Amendment Of The Act On Addictive Substances And To Amend Certain Other Acts

Original Language Title: změna zákona o návykových látkách a změna některých dalších zákonů

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273/Sb.



LAW



of 22 March. August 2013,



amending the Act No. 167/1998 Coll., on addictive substances and amending

certain other acts, as amended, and certain other

the laws of the



Parliament has passed the following Act of the United States:



PART THE FIRST



Amendment of the Act on addictive substances



Article. (I)



Act No. 167/1998 Coll., on substance abuse and on the amendment of certain other

laws, as amended by Act No 354/1999 Coll., Act No. 121/2000 Coll., Act

No 132/2000 Coll., Act No. 57/2001 Coll., Act No. 185/2001 Coll., Act

No. 407/2001 Coll., Act No. 320/2002 Coll., Act No. 222/2003 Coll., Act

No 362/2004 Coll., Act No. 228/2005 Coll., Act No. 74/2006 Coll., Act

No 124/2008 Coll., Act No. 41/2009 Coll., Act No. 141/2009 Coll., Act

No 281/2009 Coll., Act No. 291/2009 Coll., Act No. 106/2007 Coll., Act

No 341/2007 Coll., Act No. 375/2007 Coll., Act No. 18/2009 Coll., Act

No 167/2012 Coll. and Act No. 50/2013 Coll., is amended as follows:



1. § 1, including the title reads as follows:



"§ 1



The subject of the edit



(1) this Act regulates the



and treatment of addictive substances), their export, import and transit

operations with them,



(b)) treatment preparations containing addictive substance, with

containing the addictive substance, and substance of category 1 according to directly

of the applicable legislation of the European Union regulating drug precursors ^ 1)

(hereinafter referred to as "listed substance in category 1") and medicinal products

containing that substance in category 1, their export, import and

transit operations with them and



(c)), cannabis and poppy cultivation of coca and the export, import and disposal of

poppy concentrate.



(2) this Act has been notified in accordance with the directive of the European Parliament

and Directive 98/34/EC of 22 December 2004. June 1998 on the procedure for the provision

information in the field of standards and technical regulations and rules on services,

the information society, as amended. ".



2. Footnote 1 is added:



"1) European Parliament and Council Regulation (EC) No 273/2004 of 11 March.

February 2004 on drug precursors, as amended. ".



3. In paragraph 2 (a). and, § 3, paragraph 1). 2, § 5 para. 1, 2, 4 and 8, section 10, paragraph 1. 4, §

11 (1) 1 and 2, section 20 (2). 2 (a). b) to (d)), § 21 para. 2 (a). b), c)

and (e)), section 27 para. 1, § 27a para. 1 and 2, and in section 43a paragraph. 1 (b). (b) point 1)

the words "this Act" shall be replaced by "Government regulation about the list

substance abuse ".



4. In paragraph 2 (b)):



"(b)) with a solution or mixture, in any physical condition that contains

the addictive substance or the addictive substance, and substance of category 1 or

a medicine according to the law on medicinal products containing that substance

category 1 ".



5. In paragraph 2, points (c) and (d))), including footnotes # 1a and 2

shall be deleted.



Subparagraph e) to (j)) shall become point (c)) to (h)).



6. In paragraph 2 (a). (c)), after the words "Papaver somniferum" is inserted after the word "L."

at the end of the text of the letter shall be added the words ", with the exception of entire plants

poppy, including capsules, intended for ornamental purposes ".



7. In paragraph 2, points (f) and (g))) including footnote No. 2b shall be deleted.



Letter h) is renumbered as paragraph (f)).



8. In paragraph 2 (a). f), the words "and preparations containing" are replaced by

the words "and the latter, containing poppy concentrate".



9. in the heading of title II of part one: "the treatment of ADDICTIVE SUBSTANCES and

Preparations ".



10. In section 3, paragraph 3. 2 the first sentence, after the words "used to"

the words "limited research".



11. § 3a, including the title.



12. in § 5 para. 1 introductory part of the provisions, the words "or preparations

containing ephedrine and pseudoephedrine "are replaced by the words" or healing

preparations containing scheduled substances of category 1 ".



13. in section 5, the dot at the end of paragraph 1 is replaced by a comma and the following

subparagraph (c)), which read as follows:



"(c)) to prepare the pharmaceutical forms in pharmacies or pharmacists

pharmaceutical assistants under the supervision of a pharmacist. "



14. in § 5 para. 2 of the introductory part, the words "provisions and medicines

containing ephedrine and pseudoephedrine "are replaced by the words" and medicinal products

containing scheduled substances of category 1 ".



15. in § 5 para. 2 (a). and) and § 32 para. 2 the words "constitutional social

care "shall be replaced by" providing residential social services ".



16. in § 5 para. 2 (a). (c)) and in section 10, paragraph 1. 4, the words "social welfare"

replaced by the words "providing social services".



17. in § 5 para. 2 (a). (d)), the words "welfare services" are replaced by

the words "providing residential social services or doctors who are

VLA prescribing medicinal products, medical

insurance company ".



18. in § 5 para. 2 (a). g), the words "and prepare to dosage forms"

shall be deleted.



19. in § 5 para. 4, the words "and preparations containing ephedrine and

pseudoephedrine "are replaced by the words" and medicinal products containing listed

substances of category 1 ".



20. In § 5 paragraph 5 is added:



"(5) the authorisation for treatment is not required for the acquisition, storage and

processing of the cannabis plant, which can contain up to 0.3% of substances in

the Group tetrahydrokanabinolů, and only for the purposes of industrial hemp,

technical and gardening, as well as the trade in cannabis for these

purposes. ".



21. in § 5 para. 7 the second sentence, after the words "this list"

the words "and a request for amendment of the particulars referred to in the list".



22. in section 5, paragraph 7, the following paragraph 8 is added:



"(8) any changes to the information specified in the list referred to in paragraph 7 is

a person classified in the list shall be required to inform the Ministry in writing without delay

health. ".



The present paragraph 8 shall become paragraph 9.



23. in section 5, the following paragraph 10 is added:



"(10) Addictive substances referred to in annex No 3 or 4 Government regulation of

list of addictive substances and preparations containing them may without a permit to

treatment of disposing of, if they are not stored, the person on the basis of

consent granted regional authority ^ 3). To grant consent shall inform the

Regional Office, which has granted approval, the Ministry of health. This

information is given on a form issued by the Ministry of health. ".



24. In § 8 para. 1 is the number "7" shall be replaced by the number "6".



25. In section 8 paragraph 1. 2 the first sentence, the words ", or precursors"

shall be replaced by "or", and the second sentence shall be deleted.



26. in section 8 paragraph 3 reads:



"(3) the authorization to the treatment of addictive substances and preparations shall be issued

for a maximum period of 5 years. ".



27. In section 8, paragraph 5 shall be deleted.



Paragraphs 6 to 12 shall become paragraphs 5 to 11.



28. in § 8 para. 6, the second and third sentences shall be replaced by "the application shall

showing that there are



and, a copy of) the original or officially certified copy of the decision confirming the

the authorization to the treatment of drugs according to the law on pharmaceuticals or certificate of

compliance with the conditions for the performance of veterinary therapeutic and preventive activities

under the law on Chamber of veterinary surgeons,



(b)) evidence of integrity, if it is not possible under section 8a of the paragraph. 4,



c) proof of business permit,



(d)) the document containing the property owner's consent to the activities

referred to in the request,



e) contract for professional veterinary activities, if this activity

exercised,



f) proof of the provisions of the responsible person referred to in paragraph 5,



g) proof of medical fitness under section 18,



h) proof of professional competence pursuant to § 7 para. 1,



I) Declaration by the applicant that, in the case of activities which comes

into direct contact with addictive substances and preparations will be elected

the appropriate way to their security pursuant to section 10 and 11,



(j) a description of the intended production technology), in respect of an application for authorisation to

the production of addictive substances and preparations ".



29. in § 8 para. 7 and 11, § 9 para. 1, § 10 para. 1 to 3, § 14 para. 1 and

in paragraph 15 (b). (c)), the words "products and precursors" shall be replaced by "and

preparations ".



30. In section 8 shall be inserted after paragraph 8, paragraph 9, which reads as follows:



"(9) in the case of changes to the information provided in the application for a licence to

treatment related to the changes



and no longer permitted activities) or their extension,



(b)) in the name, location, legal status and identification number of the person, if it is a

a legal person, or



(c)) domicile and place of business, if different from the residence, in the case of

a natural person,



the person wishing to make these changes to submit to the Ministry of

health care a new application for the issue of permits for treatment. ".



Paragraphs 9 to 11 shall become paragraph 10 to 12.



31. in § 8 para. 10, the words "and for the reasons set out immediately

binding by a regulation of the European communities, ^ 5 c) ' shall be deleted.



Footnote # 5 c is deleted.



32. In article 8 the following paragraph 13, which read as follows:



"(1) a person who has been issued a new authorisation for treatment, is required to

return invalid authorization to the treatment of the Ministry of health up to 14

days from the date of acquisition of legal power of the new authorisation for treatment. This

the obligation also applies to persons to whom the residence permit expires

the treatment referred to in paragraph 7 and which already do not intend to continue to treat

with addictive substances and preparations; the deadline for returning the invalid permit

the treatment is 14 days from the date of expiry of the residence permit

treatment. ".




33. under section 8, the following new section 8a, which including the title reads as follows:



"§ 8a



Integrity



(1) the authorization to the treatment may be issued only to a natural person of good repute,

that has permanent residence in the territory of the Czech Republic, or good repute

a legal person with a registered office in the Czech Republic. The condition of permanent residence

or offices in the Czech Republic shall not apply in the case of a person who

has a permanent residence permit or residence, place of business, residence,

Central Administration, principal place of business or

organizational folder in the territory of another Member State of the European Union,

Contracting State to the agreement on the European economic area or the Swiss

the Confederation.



(2) the integral for the purposes of this Act, a person who was not

convicted for an intentional or negligent criminal act committed in

with regard to the treatment of addictive substances or preparations.



(3) the integrity of the shows



and an excerpt from) criminal record, not older than 3 months



1. for natural persons with permanent residence or other place of residence on the territory

The United States,



2. in the case of a natural person is or was a national of another

the Member State of the European Union or in another Member State of the European Union

has or had a place of residence,



3. for legal entities established on the territory of the Czech Republic,



(b) a similar statement from the document), criminal records



1. for natural persons with permanent residence or other place of residence outside

the territory of the Czech Republic and at the physical person in the last 5 years

continuously resided outside the territory of the Czech Republic for more than 6

months; document comparable to extract from the criminal register must be

issued by the competent authority of the State of permanent or other residence of this

persons, States in which this person in the past 5 years

continuously resided for more than 6 months, and a State which is not

the same as the State of permanent residence or other residence of that person and this

the person is its citizen,



2. in the case of a legal person located outside the territory of the Czech Republic; document

similar to the extract from the criminal register must be issued to

the legitimate authority of the State of the registered office,



(c) a sworn declaration of integrity)



1. in the case of a natural person, the State of permanent residence or other residence

natural persons and the State, where the natural person in the last 5 years

the 24-hour visa, the document referred to in subparagraph (b)); affidavit of

integrity must be made before a notary public or by the competent authority

the State of permanent or other residence of that person and States in which the

This person in the past 5 years continuously resided for a period longer

than 6 months,



2. in the case of a legal person, does not make the State of the seat of the legal person document

referred to in subparagraph (b)); affidavit of integrity must be made

before a notary public or by the competent authority of the State of residence.



(4) in order to demonstrate the integrity of the persons referred to in paragraph 3 (b). and)

1 and 3, the Ministry of health provides under a special legal

prescription ^ 5f) an extract from the criminal register. Extradition request listing

of convictions and an extract from the criminal register with

to be transmitted in electronic form, in a manner allowing remote

access. The Ministry of health may obtain any other

supporting documents, where necessary to verify the information referred to in paragraph

3. ".



34. In § 9 para. 1 the first sentence, the words "§ 8 para. 6 "shall be replaced by the words" §

8 (2). 5. "



35. In § 9 para. 4, the third sentence shall be deleted.



36. In § 9 paragraph 6 is added:



"(6) a person issued a permit to the treatment, is required to

to ensure that the activities to which the permit is required treatment,

will not be carried out without the consent of the responsible person. ".



37. In § 9 para. 9 the first sentence, the words "§ 8 para. 6 "shall be replaced by the words" §

8 (2). 5. "



38. In § 9 para. 9 second sentence, the words "Ministry of health"

replaced by the words "on a form issued by the Ministry of health".



39. In paragraph 11 (1) 1 and 2, the words "preparations containing them, and

precursors "shall be replaced by" and products containing them ".



40. In paragraph 11 (1) 2, the words ", or precursors" shall be replaced by

the words "and preparations".



41. section 12 including the title reads as follows:



"section 12



Shop



Addictive substances and preparations can be passed or sold only to persons

entitled to dealing with them. The same applies to the transfer of other

the rights associated with addictive substances and preparations ".



42. In article 13, paragraph 1 reads:



' (1) medicinal product in accordance with the law on medicinal products (hereinafter referred to as "medicinal

preparation "), which contains an addictive substance or substance

category 1, may be issued to a person at the pharmacy, which has not been issued

the authorization to the treatment, only on the recipe, requisition, or no prescription with

restrictions under the law on pharmaceuticals ^ 6a). In the case of a medicinal product,

that contains an addictive substance referred to in annex No. 1 or 5 of regulation

Governments on the list substance abuse, may be issued only on a prescription or

requisition marked blue stripe, oriented from bottom left to

the upper right corner, or exclusively on electronic recipe, where

so the law on pharmaceuticals ^ 6). If this is about a medicine that contains

the addictive substance referred to in annex No. 1 or 5 Government regulation about the list

substance abuse and which is also included in annex 8 of regulation

Governments on the list substance abuse, may be issued in a pharmacy on prescription

or requisition without marking blue stripe. ".



43. In section 13 paragraph 10 is added:



"(10) a medicine that contains an addictive substance or listed

substance in category 1, shall not be issued repeatedly to one recipe. ''.



44. In the title of § 14, § 14 para. 2 and 3 and in paragraph 35, the words ", and

precursors "shall be replaced by" and preparations ".



45. In section 14 is at the end of paragraph 1, the following sentence "the person performing the

disposal of unusable addictive substances and preparations and wastes is

containing about draws up write. ".



46. In article 14, the following paragraph 4 is added:



"(4) in the treatment of inoperable addictive substances and preparations,

as well as waste containing, proceed as in the

management of hazardous wastes, including the keeping of records referred to in

the law governing waste management. ".



47. In paragraph 15 (b)) shall be deleted.



Subparagraph (c)) to (g)) shall become point (b)) to (f)).



48. In paragraph 15 (b). (d)), after the words "Papaver somniferum" is inserted after the word "L.".



49. In article 15, subparagraph (f)):



"(f)) advertising on addictive substances and preparations (EOU) support

the public under the law governing the regulation of advertising ".



50. section 16, including title and footnotes # 5e, and 7 c shall be deleted.



51. In Title III of part one: "eligibility for treatment

ADDICTIVE SUBSTANCES AND PREPARATIONS ".



52. In § 17 paragraph 2. 1 the first sentence, the words "(§ 8 paragraph. 5) ' shall be deleted and the phrase

the second is replaced by the phrase "Integrity shall be demonstrated in a manner pursuant to §

8A. ".



53. In paragraph 19 (1):



' (1) as the responsible person can appoint a natural person who

She graduated from the master's degree programme in one of the following

areas:



and) pharmacy,



(b)) General Medicine, dental medicine, dentistry,



(c)) chemistry, or



d) veterinary medicine. ".



54. In section 20 (2). 2 (a). and) and in section 21 para. 2 (a). and) the words "to

This Act "shall be replaced by" Government regulation about the list of substance abuse

substances ".



55. In section 20 (2). 2 (a). and the words "or) preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".



56. In section 20 (2). 2 (a). (b)), the words "or preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".



57. In section 20 (2). 2 (a). (b)), the words "or preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".



58. In section 20 (2). 2 (a). (c)), the words "or preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".



59. In section 20 (2). 2 (a). (d)), the words "or preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".



60. In section 20 (2). 2 letter e) is added:



"e) to the export of the cannabis plant, which can contain up to 0.3% of the substances

tetrahydrokanabinolů group for industrial, technical and horticultural

purposes. ".



61. section 20a and 20b, including headings and footnotes # 8b shall be deleted.



62. In section 21 para. 2 (a). a) and (c)), the words "or preparations containing

ephedrine or pseudoephedrine, "shall be replaced by the words" or medicinal products

containing scheduled substances of category 1, ".



63. In section 21 para. 2 (a). (b)) and in section 26 para. 1 (b). (c)), the words "or

preparations containing ephedrine or pseudoephedrine "shall be replaced by

"or medicinal products containing substances listed in category 1".



64. In § 21 para. 2 (a). (b)), the words "or preparations containing

ephedrine or pseudoephedrine "are replaced by the words" or medicinal products with

containing scheduled substances of category 1 ".




65. In § 21 para. 2 letter d) is added:



"(d)) to the importation of the cannabis plant, which can contain up to 0.3% of the substances

tetrahydrokanabinolů group for industrial, technical and horticultural

purposes ".



66. In § 21 para. 2 (a). e), the words "or medicinal products

containing ephedrine or pseudoephedrine, "shall be replaced by the words" or

medicinal products containing substances listed in category 1, ".



67. In § 21 para. 4 and in section 43a paragraph. 3 (b). e), the words "of the products,

precursors or auxiliary substances of category 2 and 3 by directly

of the applicable legislation of the European communities ^ 2) "shall be replaced by the words" and

preparations ".



68. In paragraph 22 of the paragraph. 3 the first sentence with the number "6" is replaced by "3" and in the

the third sentence, the words "made available" are deleted.



69. under the first heading of title V shall read: "cannabis, COCA, OPIUM POPPY and

The SAME WAY ".



70. the heading of section 24 reads as follows: "cannabis, coca and opium poppy".



71. In paragraph 24 of the letter a) is added:



"a) grow the plant species and varieties of hemp (Cannabis genus) that can

contain more than 0.3% of the substances from the Group of tetrahydrokanabinolů, with

exception of cultivation on the basis of the license granted under this Act;

the ban does not apply to the cultivation of varieties of the cannabis plant (genus Cannabis)

for research purposes, for breeding new varieties and for maintaining the

genetic diversity of scientific and research institutions established

by law or by the State, as defined in the authorization to the treatment ".



72. In paragraph 24, at the end of subparagraph (b)) the dot replaces the comma and the following

subparagraph (c)), which read as follows:



"(c)) to grow varieties of opium poppy (Papaver somniferum l.), which may, in

the dry matter of the capsules contain not more than 0.8% of morphine; prohibition does not apply

on the cultivation of varieties of opium poppy (Papaver somniferum l.) for research and

experimental purposes, for the cultivation of new varieties of plants, and for maintaining the

genetic diversity of plants by scientific and research institutions. ".



73. In paragraph 24 of the present text shall become paragraph 1 and the following

paragraphs 2 and 3 shall be added:



"(2) the person cultivating opium poppy (Papaver somniferum l.) or a person who

makovinu is processed or stored, is also obliged to immediately notify the

the locally competent Department of the police of the Czech Republic all suspected

circumstances, in particular the entry of foreign people to the stand, cutting, the poppies

the theft of the poppies or unusual orders, which indicate that the same

can be used for the illicit manufacture of drugs.



(3) the same produced in the territory of the Czech Republic must be exported

or is incapacitated or is processed so that it contained the addictive substance

It was not possible to use or acquire any technology

resources. ".



74. In section 26 para. 1 (b). a), the words "and preparations," the words

"disposal," and at the end of the text of the letter shall be added the words ", if

These persons in the past calendar year with these substances shall not treat,

It is sufficient to notify this fact to the Ministry of health ".



75. In section 26 para. 1 (b)):



"(b)) to the end of April, an estimate of the production, cultivation and importation of the substance abuse and

preparations in the next calendar year; for the products listed in the annex

# 8 Government regulation about the substance list shall indicate only an estimate of the

production; in the case above the initial estimate of production and

the import of these persons are obliged to estimate production and importation without delay

increase; These estimates may be adapted ^ 10b) by the International Bureau for the

Narcotics Control Board ^ 2a) ".



76. In section 26 para. 4, the last sentence is replaced by the phrase "die

entrepreneurial natural person who has been issued a permit to the treatment,

obligation to submit a special report shall be transferred pursuant to paragraph 1. and) on

the responsible person or its representative and in the case that these persons

cannot meet this obligation, then passes to the heritage Manager. ".



77. In section 27 is at the end of paragraph 1, the following sentence "If these persons in

the past calendar year shall not treat with these substances, it is sufficient that

notify in writing to the State Institute for drug control. ".



78. In paragraph 27a para. 1 the first sentence, the words "competent regional veterinary

manage or urban health administration in Prague "are replaced by the words" Institute

for State control of veterinary Biologicals and medicaments (hereinafter referred to as

"The animal health Institute") "and the second sentence shall be replaced by the phrase" message

Veterinary Institute on a form served lished. ".



79. In article 27a, paragraph 2 shall be deleted.



The former paragraph 3 shall become paragraph 2.



80. Under section 27a para. 2 the words "Institute for State control of veterinary

Biologicals and pharmaceuticals "is replaced by" Veterinary Institute ".



81. § 28, including the title.



82. In paragraph 29 (b). and) point 1 shall read:



"1. the assessment of land sown with poppy seeds or cannabis varieties for harvest in

the calendar year, including the name of the varieties used ^ 10 g), numbers

parcel number, name, and cadastral territory ^ 10 h), or identification

soil block numbers, or the part of the soil block land parcel ^ 10i) ".



83. the footnote # 10 g:



"10 g) Act No. 218/2003 Coll., on marketing of seeds and plants

cultivated plants and amending some laws (law on the circulation of the seed and

seed), as amended. ".



84. In paragraph 29 (b)):



"(b)) in the vegetation and harvest or during the disposal of harvested

data on the area of poppy concentrate land and how the destruction of opium poppy,

poppy concentrate left on land or harvested or hemp, including the name of

registered varieties used ^ 10 g), parcel number, name, and numbers

cadastral territory ^ 10 h) or identification number of the soil block

where applicable, a part of the soil block, evidence of soil ^ 10i), no later than 5

days before performing their disposal; If the person cultivating opium poppy

reverse does not remove the makovinu coming from the treated seeds, passes

obligation to transmit reports during the disposal of poppy concentrate on a person who

cleaning poppy seeds ".



85. In § 31 para. 1 the words "competent regional veterinary

administrations or Public Health Administration in Prague "is replaced by

"Veterinary Institute".



86. In article 32, paragraph 1 shall be deleted.



Paragraphs 2 and 3 shall become paragraphs 1 and 2.



87. In § 33 para. 1 the words "preparations, precursors and auxiliary

substances of category 2 and 3 according to the applicable regulations of the European right

Community ^ 1) "is replaced by" and "and the words", and in the case of

precursors and auxiliary substances of category 2 and 3 according to the directly applicable

regulations of the European Communities ' ^ 1 ') for at least 3 years ^ 10n) "

shall be deleted.



88. In § 34 paragraph 1 reads:



"(1) the checking of compliance with the obligations arising from this Act and of the

decision issued on its basis shall carry out



and) authorized employees



1. the Ministry of health,



2. The State Institute for drug control in matters relating to pharmacies and

treatment with cannabis for medicinal use,



3. regions of inclusion in the regional office, if it is not about control of pharmacies, and

Furthermore, in matters relating to the inspection referred to in section 13 and 14,



4. The animal health Institute,



(b)) members



1. the police of the Czech Republic,



2. the customs administration of the Czech Republic in matters relating to poppy cultivation

linseed and hemp and in matters relating to compliance with the obligations arising from article 11,



(hereinafter referred to as "inspectors"). ".



89. In § 34 paragraph 1. 6, the word "write" is replaced by the word "Protocol".



90. section 36 including the title reads as follows:



"§ 36



Administrative offences



(1) a legal entity or individual entrepreneur is committed by the administrative

tort by



and) contrary to section 4 pursues an activity that requires a permit to

treatment, without this authorisation,



b) contrary to section 5 (3). 8 do not notify the Ministry of health change

the data referred to in the list,



c) contrary to section 8 (2). 2 manufactures addictive substances or preparations of

maximum available refund volume laid down in the authorization to the treatment,



(d)) in the application for the authorization to the treatment administered pursuant to section 8 (2). 6 shall be

incorrect or incomplete data,



e) contrary to section 8 (2). 7 absence of the Ministry of health in writing

an application for a new permit for treatment no later than 6 weeks prior to the

the expiry date of an existing authorisation for treatment,



f) contrary to section 8 (2). 8 do not communicate in writing to the Ministry of health

change of information contained in the request for authorization to the treatment,



g) has requested the release of the new permits for treatment in the case of some of the

changes to the data referred to in the request for authorization to the treatment provided for under section 8

paragraph. 9,



h) contrary to section 8 (2). 11 has not notified of termination of the activity to which it

the authorization to the treatment,



I) contrary to section 8 (2). 13 Department of health does not return void

the authorization to the treatment within 14 days from the date of acquisition of legal power of the new

the authorization to the treatment,



j) in violation of § 9 para. 9 to notify in writing the Ministry of health

appointment of a representative of the responsible person or termination of its functions,



k) in violation of § 9 para. 10 does not appoint a responsible person in the

the prescribed period or has requested the Ministry of health about the change

the authorization to the treatment,



l) contrary to section 10 of the stores of addictive substances and preparations, as well as

the equipment for their production or cultivation,




m) contrary to section 11 transports the addictive substances listed in the annexes 1,

2, 3 or 5 Government regulation about the list of addictive substances and preparations is

tagged,



n) contrary to section 12 of the passes or sells addictive substances and preparations or

other rights associated with addictive substances and preparations,



about) as the person referred to in § 5 para. 2 (a). a) or b) fails

debased forms of the recipes or requisitions with a blue stripe municipal

Office of the municipality with extended competence pursuant to § 13 para. 6,



p) as a person who no longer meets the conditions laid down in § 5 para. 2

(a). and) or (b)), does not relinquish unused or degraded forms

recipes or requisitions with a blue stripe within 5 days of the village Municipal Council

extended jurisdiction pursuant to § 13 para. 7,



q) contrary to § 14 para. 1 does not make a disposal of unusable

addictive substances and preparations or wastes containing,



r) contrary to section 15 (b). and) places the addictive substances and preparations in

customs warehouses, free zones or free warehouses

warehouses,



with the breach of any of the prohibitions), pursuant to section 15 (b). (b)),



t) contrary to section 20 (2). 1 take the addictive substances or preparations without

export permit



u) contrary to section 21 para. 1 takes the addictive substances or preparations without

import permit,



in the request) an export or import permit, in accordance with section 22 paragraph 1. 2

incorrect or incomplete information shall,



w) does not return the Ministry of health of the export or import authorisation

According to section 22 para. 3,



x) violates the ban to cultivate cannabis plant species or variety (genus

Cannabis), which can contain no more than 0.3% of the substances from the Group of

tetrahydrokanabinolů, pursuant to § 24 para. 1 (b). a), or



s) violates the ban to cultivate opium poppy varieties, which may, in the dry matter of the

capsules contain more than 0.8% of morphine, according to § 24 para. 1 (b). (c)).



(2) a legal entity or individual entrepreneur is committed by the administrative

tort by



and growing as a person), opium poppy or the person handling or

to notify immediately the police holding the makovinu of the Czech Republic

the circumstances pursuant to § 24 para. 2,



b) contrary to section 24 para. 3 inactivate or reflects the makovinu poppy

field vyprodukovanou on the territory of the Czech Republic,



c) contrary to section 25 para. 1 ride or makovinu without the import export

or export permit



(d)) in the application for an export permit or a permit to import poppy concentrate

poppy concentrate according to § 25 para. 1 indicate incorrect or incomplete data,



e) as the person who is authorised to deal with addictive substances and

preparations on the basis of the authorization to the treatment, fail to comply with any of the

reporting obligations pursuant to section 26 paragraph 1. 1 or 3, or in the report shall be

incorrect or incomplete data,



(f)) as a person, that its action does not require a licence to

treatment of addictive substances and preparations according to § 5 para. 7, fails to comply with

one of the reporting obligations in accordance with § 26 para. 2,



g) contrary to section 30 does not pass the Ministry of health to the 15th

the first day of the month following the calendar quarter quarterly

reports on the export or import of poppy concentrate in the previous quarter, or in

reports indicate incorrect or incomplete data,



(h) fails to fulfil any of the obligations) under § 32 para. 1 or § 33 para. 1,



I) fails to comply with the control or the obligation of notification under section 35, or



(j)) does not use the names of addictive substances and preparations according to § 42.



(3) a legal entity or individual entrepreneur, which provides

Pharmacy, health services, committing an administrative offense further by



and) contrary to section 27 para. 1 does not pass to the State Institute for drug control

by the end of February, the annual report for the previous calendar year and status

movement of stocks of addictive substances listed in Appendix 1 or 5 of regulation

Governments on the list of addictive substances, including products containing,

exception of those mentioned in annex No. 8 on the list of government regulations

substance abuse,



b) contrary to section 27 para. 1 shall indicate in its annual reports on the status and movement of

stocks of addictive substances listed in Appendix 1 or 5 of regulation of the Government of

list of addictive substances, including products containing them, with the exception of

products listed in annex No. 8 on the list of government regulation of addictive

substances, for the previous calendar year of incorrect or incomplete information, or



c) in contravention of section 27 para. 2 upon termination of the activities of the pharmacy does not pass

The State Institute for drug control of emergency status report and movement

stocks of addictive substances listed in Appendix 1 or 5 of regulation of the Government of

list of addictive substances, including products containing them, with the exception of

products listed in annex No. 8 on the list of government regulation of addictive

substances, or in the report indicate incorrect or incomplete data.



(4) a legal entity or individual entrepreneur, which provides

Pharmacy, health services or distributes pharmaceuticals, is guilty of an

the administrative offense further by



and) contrary to section 27a para. 1 does not report to a 10. January of the calendar year

Veterinary Institute of preparations containing addictive substances collection

referred to in annexes 1 and 5 Government regulation about the list of addictive substances,

with the exception of those listed in annex No. 8 on the list of government regulations

substance abuse, veterinarians for the previous calendar year, or



b) contrary to section 27a para. 1 shall indicate in the report about the subscription products

containing addictive substances referred to in annexes 1 and 5 of the regulation of the Government

about the list of addictive substances, with the exception of the products listed in annex No.

8 Government regulation about the list of substance abuse, for veterinarians

the previous calendar year of incorrect or incomplete information.



(5) a legal entity or individual entrepreneur, which cultivates opium poppy

or hemp on a total area larger than 100 square meters, is guilty of an administrative

tort by



and) contrary to section 29 does not fulfil the obligation, or



(b)) provide inaccurate or incomplete information in the reports referred to in section 29.



(6) a legal entity or individual entrepreneur, which was awarded to the

the licence for the cultivation of cannabis for medicinal use, is guilty of an administrative

tort by breach of an obligation under section 24a of para. 4 (b). and), (b)),

(c)), d), (e)), or (f)) or under section 24b para. 1. ".



91. In section 37 paragraphs 1 and 2 shall be added:



"(1) for the administrative offence under § 36 odst. 1 shall be imposed to



and 500 000 CZK), in the case of an administrative offence referred to in subparagraph (b)), (c)), e) to (h)),

j) to q)), x) or y),



(b)) 1 000 000 CZK in the case of an administrative offence referred to in subparagraph (d)), i, t)))

or w),



(c) Eur 10 000 000), in the case of an administrative offence under (a)), r) or s).



(2) an administrative offence under § 36 odst. 2 500 000 imposed in

CZK. ".



92. In article 37, paragraphs 5, 6 and 8 shall be deleted and paragraph 7,

becomes paragraph 5.



93. In paragraph 37, paragraph 5 is added:



"(5) for the administrative offence under § 36 odst. 5, fined the



and 500 000 CZK), in the case of an administrative offence referred to in subparagraph (b)),



(b)) 1 000 000 CZK in the case of an administrative offence under (a)). ".



94. In paragraph 37, the following paragraph 6 is added:



"(6) for the administrative offence under § 36 odst. 6, imposed to 1 000 000

CZK. ".



95. section 38, including the title reads as follows:



"§ 38



Forfeiture of things



For the administrative offence under section 36, you can save the confiscation of substance abuse and

products, equipment, and materials needed for their manufacture or

growing, if the perpetrator belongs to an administrative offense and



and) were for committing an administrative offense intended,



(b)) have been used to an administrative offence,



(c) committing an administrative offense) were obtained, or



(d)) they were acquired as a matter of administrative tort acquired. ".



96. Section 38 shall be added to § 38a, which including the title reads as follows:



"§ 38a



Prevents things



If no saved confiscation referred to in § 38, you can decide that the

such a thing works, if the offender belongs, which can't be for administrative

offence to prosecute, or does not belong to the perpetrator of the administrative offense or his

does not belong in full, and if required by the safety of persons, property or other

the general interest. ".



97. In section 39 paragraph 2 reads as follows:



"(2) for the offense referred to in paragraph 1 (b). and you can impose a fine to) 100

EUR and for the offense referred to in paragraph 1 (b). (b) impose a fine to) can be used

200 000 Kč. You can control the page block for the offense referred to in paragraph 1 save

a fine of up to CZK 5,000. ".



98. In § 40 paragraph 4 to 7 shall be added:



"(4) administrative offenses under § 36 odst. 1 and 2, with the exception of the administrative

offences under § 36 para. 1 (b). l) and q), committed in the health

facilities including a pharmacy, according to § 36 odst. 1 (b). m), o), p, r)), x) and

s) and in accordance with § 36 odst. 2 (a). a), b), (h) and (i))), in the first instance

discusses the Ministry of health.



(5) administrative offenses under § 36 odst. 1 (b). l), o), p) and (q)) and under section

paragraph 36. 2 (a). h) and (i)), committed in a medical facility outside of the

Pharmacy, in the first instance dealt with regional office.



(6) administrative offenses under § 36 odst. 1 (b). l) and (q)) and pursuant to § 36 odst.

2 (a). h) and (i)), committed in a pharmacy, and in accordance with § 36 odst. 3 (b). a), (b))

and (c)) and in accordance with § 36 odst. 6 in the first instance dealt with the State Institute of

drug control.



(7) administrative offenses under § 36 odst. 1 (b). m), r), x and y)), section 36

paragraph. 2 (a). a) and b) and in accordance with § 36 odst. 5 (b). a) and b) and misdemeanors

pursuant to § 39 para. 1 (b). a) and b) in the first instance hearing of the customs

administration of the United States. ".




99. In section 40 para. 8, the words "competent regional Veterinary Administration or

City Veterinary Administration in Prague "are replaced by the words" the animal health

the Institute ".



100. In paragraph 2 of section 40. 11, after the words "Customs authorities" shall be replaced

"The State Institute for drug control," and the words "competent regional

Veterinary administrations or Public Health Administration in Prague "

replaced by the words "Veterinary Institute".



101. In paragraph 41, § 43a paragraph. 1 and 2, and in section 43a paragraph. 3 (b). and the words "),

products, precursors and auxiliary substances of category 2 and 3 by directly

applicable regulations of the European Communities ' ^ 1 ') "shall be replaced by the words" and

preparations ".



102. section 41a shall be deleted.



103. In paragraph 42 the first sentence, the words "to this Act, in the case of precursors

and auxiliary substances of category 2 and 3 according to the names of directly applicable

regulations of the European Communities ' ^ 1 ') "shall be replaced by ' the regulation of the Government of

list of addictive substances ".



104. In section 43 paragraph 1 reads:



"(1) the ministries and other central administrative authorities shall cooperate with the

The Ministry of health to the extent arising from their scope

in the preparation of documentation for



and international organizations about the treatment) with addictive substances and preparations,



(b)) new proposals for inclusion of substances between the addictive substances to the annexes

the Government Decree on the list of substance abuse. ".



105. In § 43 para. 2 the words "products and precursors" shall be replaced by

the words "and preparations".



106. In § 43 para. 3 and § 43a paragraph. 3 the words "Customs authorities" shall be replaced by

the words "Authorities of the customs administration of the Czech Republic."



107. In § 43 para. 4 (b). (c)), the word "January" is replaced by

"March".



108. In § 43 para. 5 (b). (c)) and in § 43 para. 6 (a). (b)), the words "31.

March ' is replaced by ' 30. April ".



109. In § 43 para. 7 (b). and) point 1 and section 43 para. 7 (b). (b)), the words

"or precursors" shall be deleted.



110. In paragraph 43, at the end of paragraph 8, the period is replaced by a comma and the following

the letter d), which read as follows:



"(d)) shall inform the Ministry of health about the checks carried out in

pharmacies and instituted administrative proceedings conducted on the basis of

violation of obligations established by this Act, to 30. April, 31.

July, 30. October and 31. January for the previous calendar quarter. ".



111. In § 43a paragraph. 1, letter a) is repealed.



Subparagraph (b)) to (f)) are known as letters a) to (e)).



112. In § 43a paragraph. 1 (b). and), after the words "regional authority" be inserted

the words "and the State Institute for drug control", and at the end of the text of the letter

shall be added the words "and 6".



113. In Article 43a paragraph. 1, points (c) and (d))), including footnotes, no.

11j and 11 k deleted.



Letter e) is renumbered as paragraph (c)).



114. In § 43a paragraph 2 reads as follows:



"(2) the police of the Czech Republic



and the Ministry of health about) informs all important

the facts necessary for their decisions under this Act,

in particular, about the theft of addictive substances and preparations and their attempts

theft,



(b) may at any time) is a remotely through a specified contact

the workplace in case of detection of cannabis or cannabis-containing product for

person to object to the request to the registry for medicinal products with restrictions

served according to the law on pharmaceuticals ^ 6), whether that person be conducted between

persons who have been issued individually prepared medicinal product with the

content of cannabis for medicinal use; such request register

without delay and free of charge, will match the desired value; in the case that it is

This person conducted between persons who have been issued individually

prepared a medicine containing cannabis for medicinal use,

Furthermore, the registry free of charge shall notify the date of issue and the total issued amount

individually prepared medicinal product containing cannabis for

medicinal use. ".



115. In § 43a paragraph. 3, points b) to (d)), including footnotes, no.

11o and 5 p deleted.



Letter e) is renumbered as paragraph (b)).



116. section 44, including the title reads as follows:



"§ 44



Common provisions



Appeal lodged against the decision on the withdrawal of authorisation for the treatment of

the withdrawal of an export permit, import permit, on the withdrawal of the withdrawal

an export permit poppy concentrate and the withdrawal of licences to poppy concentrate has

suspensory effect. ".



117. In section 44b the words "§ 8 para. 7 and 11 "shall be replaced by the words" § 8 para. 6 and

11 ", the words" § 16 para. 1, § 28 para. 3 "shall be deleted and the words" § 25 para.

1 "shall be replaced by the words" § 25 para. 2. "



118. the following section is inserted after section 44b 44 c, including the title reads as follows:



"§ 44 c



Powers of execution



(1) the Government shall determine by regulation



and) list



1. the narcotic drugs listed in Schedule I in accordance with the single Convention on

narcotic drugs and



2. other drugs, which is due to the extent of their

abuse or because they directly or indirectly jeopardize the health,

necessary to provide treatment on the basis of the authorization to the treatment, or is

for this reason, you must ensure that the medicinal products containing these

the substances were emitted in the pharmacy only on a prescription or requisition marked

blue stripe, oriented from bottom left to the top right corner,



(b)) list



1. the narcotic substances included in List II of the single Convention on

narcotic drugs and



2. other stupefying substances for which there is, because of the extent of their

abuse or because they directly or indirectly jeopardize the health,

must ensure that medicinal products containing these substances are

issued in a pharmacy on prescription or requisition without marking the blue line



(c)) list



1. the narcotic substances included in list IV in accordance with the single Convention on

narcotic drugs and



2. other stupefying substances for which there is, because of the extent of their

abuse or because they directly or indirectly jeopardize the health,

necessary to ensure that substances and preparations containing these other narcotic

substances have been used only to a limited research, scientific and very

limited therapeutic purposes defined in the authorization to the treatment,



(d)) list



1. psychotropic substances included in list I of the Convention

psychotropic substances and



2. other psychotropic substances, for which, because of the extent of their

abuse or because they directly or indirectly jeopardize the health,

necessary to ensure that substances and preparations containing these additional

psychotropic drugs were used only to limited research, scientific

and very limited therapeutic purposes defined in the authorization to the treatment,



e) list



1. psychotropic substances included in list II in accordance with the Convention on the

psychotropic substances and



2. other psychotropic substances, which is due to the extent of their

abuse or because they directly or indirectly jeopardize the health,

necessary to provide treatment on the basis of the authorization to the treatment, or is

for this reason, you must ensure that the medicinal products containing these

the substances were emitted in the pharmacy only on a prescription or requisition marked

blue stripe, oriented from bottom left to the top right corner,



f) the list of psychotropic substances included in the list (III) under the Convention on

psychotropic substances,



g) list



1. psychotropic substances included in the list (IV) under the Convention on

psychotropic substances and



2. other psychotropic substances, for which, because of the extent of their

abuse or because they directly or indirectly jeopardize the health,

must ensure that medicinal products containing these substances are

issued in a pharmacy on prescription or requisition without marking the blue line, and



h) list of the included in the list according to the single Convention on

narcotic drugs.



(2) the Government shall state the list by



and paragraph 1 (a)). and) in annex 1 to the regulation referred to in paragraph 1,



(b) paragraph 1 (a)). (b)) in annex 2 to the regulation referred to in paragraph 1,



(c) paragraph 1 (a)). (c)) in annex No. 3 to the regulation referred to in paragraph 1,



(d) paragraph 1 (a)). d) in annex 4 to the regulation referred to in paragraph 1,



e) to paragraph 1. e) in the annex 5 to the regulation referred to in paragraph 1,



f) to paragraph 1. (f)) in annex No 6 to the regulation referred to in paragraph 1,



(g) paragraph 1 (a)). g) in Appendix 7 to the regulation referred to in paragraph 1 and



(h)) to paragraph 1. h) in annex No. 8 to the regulation referred to in paragraph 1.



(3) the Ministry of agriculture to implement section 24 establishes by decree a list of

opium poppy varieties that meet the condition of maximum 0.8% content

morphine in the dry matter of the capsules, and the method of disposal of poppy concentrate. ".



119. The annex No. 1 to 8 shall be deleted.



Article. (II)



Transitional provision



The last calendar year in which you can grow and harvest varieties

opium poppy (Papaver somniferum l.) that can in the dry matter of the capsules

contain more than 0.8% of morphine is the calendar year following the

the year in which this law came into effect, with the exception of cultivation and

harvest varieties of opium poppy (Papaver somniferum l.) for research and

experimental purposes, for the cultivation of new varieties of plants, and for maintaining the

genetic diversity of plants by scientific and research institutions.



PART TWO



Amendment of the Act on administrative fees



Article. (III)



The annex to the Act No 634/2004 Coll., on administrative fees, as amended by


Act No. 217/2005 Coll., Act No. 228/2005 Coll., Act No. 357/2005 Coll.

Act No. 361/2005 Coll., Act No 444/2005 Coll., Act No. 545/2005 Coll.

Act No. 553/2005 Coll., Act No. 48/2006 Coll., Act No. 56/2006 Coll.

Act No. 57/2006 Coll., Act No. 81/2006 Coll., Act No. 109/2006 Coll.

Act No. 112/2006 Coll., Act No. 130/2006 Coll., Act No. 135/2006 Coll.

Act No. 137/2006 Coll., Act No. 159/2006 Coll., Act No. 179/2006 Coll.

Act No. 186/2006 Coll., Act No 215/2006 Coll., Act No. 227/2006 Coll.

Act No 227/2006 Coll., Act No. 235/2006 Coll., Act No. 309/2006 Coll.

law no 575/2006 Coll., Act No. 106/2007 Coll., Act No. 261/2007 Coll.

Act No. 269/2007 Coll., Act No. 374/2007 Coll., Act No. 379/2007 Coll.

Act No. 38/2008 Coll., Act No. 130/2008 Coll., Act No. 140/2008 Coll.,

Act No. 182/2008 Coll., Act No. 189/2008 Coll., Act No. 230/2008 Coll.,

Act No. 239/2008 Coll., Act No. 254/2008 Coll., Act No. 297/2008 Coll.,

Act No. 297/2008 Coll., Act No. 301/2008 Coll., Act No. 309/2008 Coll.,

Act No 312/2008 Coll., Act No. 382/2008 Coll., Act No. 9/2009 Coll.,

Act No. 141/2009 Coll., Act No. 197/2009 Coll., Act No. 207/2009 Coll.,

Act No. 227/2009 Coll., Act No. 281/2009 Coll., Act No. 291/2009 Coll.,

Act No. 301/2009 Coll., Act No. 346/2009 Coll., Act No. 420/2009 Coll.,

Act No. 132/2010 Coll., Act No. 148/2010 Coll., Act No. 153/2010 Coll.,

Act No. 160/2010 Coll., Act No. 343/2010 Coll., Act No. 427/2010 Coll.,

Act No. 30/2011 Coll., Act No. 105/2007 Coll., Act No. 133/2007 Coll.

Act No. 134/2007 Coll., Act No. 152/2007 Coll., Act No. 188/2007 Coll.

Law No 245/2007 Coll., Act No. 249/2011 Coll., Act No. 255/2007 Coll.

Law No. 262/2007 Coll., Act No. 300/2011 Coll., Act No. 308/2007 Coll.

Act No. 329/2011 Coll., Act No. 344/2007 Coll., Act No. 349/2007 Coll.

Act No. 350/2011 Coll., Act No. 357/2010 Coll., Act No. 367/2007 Coll.

Law No 375/2007 Coll., Act No. 428/2007 Coll., Act No. 457/2011 Sb.

Act No. 458/2011 Coll., Act No. 472/2010 Coll., Act No. 19/2009 Coll.,

Act No. 37/2009 Coll., Act No. 53/2010 Coll., Act No. 119/2009 Coll.,

Act No. 169/2009 Coll., Act No. 172/2009 Coll., Act No. 202/2009 Coll.,

Act No. 221/2009 Coll., Act No. 225/2012 Coll., Act No. 274/2009 Coll.,

Act No. 350/2012 Coll., Act No. 359/2012 Coll., Act No. 399/2012 Coll.

law no 407/2009 Coll., Act No. 428/2009 Coll., Act No. 496/2012 Coll.

Act No. 502/2012 Coll., Act No. 503/2012 Coll., Act No. 50/Sb.

Act No. 69/2013 Coll., Act No. 102/2013 Coll., Act No. 170/Sb.

Act No. 185/2013 Coll. and Act No. 186/2013 Coll., is amended as follows:



1. In part VI of item 100, including footnote # 59:



"Item 100



and the issue of permits to treatment) drugs,

psychotropic substances or preparations ^ 59) Kč5 000



(b)) licence to export or import of narcotic drugs,

psychotropic substances or preparations ^ 59), Czk1, 000



(c)) licence to export or import of poppy concentrate $ 500



59) Act No. 167/1998 Coll., on addictive substances and amending certain

other acts, as amended. ".



2. in part VI of the 100 item following item 100A, which including

footnote # 77:



"Entry 100A



and the issue of a licence to the business) with a scheduled substance of category 1

According to the law on drug precursors, and by directly applicable

European Union legislation regulating drug precursors ^ 77) EUR 3 000



(b) the issue of a licence to the business) with a scheduled substance of category 1

According to the law on drug precursors, and by directly applicable

European Union legislation regulating drug precursors ^ 77) Court

Toxicology Laboratory, the laboratory of the Health Institute,

specialised diagnostic, scientific-research

or workplace learning university or public research

institution in accordance with the Act on public research institutions-$ 1,000



(c) a special edition of the licences for) an activity with a scheduled substance of category 1

According to the law on drug precursors, and by directly applicable

European Union legislation regulating drug precursors ^ 77)

care provider $ 500

for each place of business listed

in the request for a special license



(d) the issue of a new licence) because of a change in the particulars specified

in the licence pursuant to the Act on drug precursors, and by directly

applicable European Union legislation governing precursors

drugs ^ 77) or extend the licence under the Act on drug precursors CZK 2 000



(e)) because of the change to change the license of the person responsible, the changes

first or last name of the person responsible or changes of registered office,

residence, name, trade name or in the name or surname of the holder

a licence under the Act on drug precursors and by directly

applicable European Union legislation regulating drug precursors ^ 77) $ 1,000



(f) the issue of a new licence) because of a change in the particulars specified

in the licence pursuant to the Act on drug precursors, and by directly

applicable European Union legislation regulating drug precursors ^ 77)

or extend the licence under the Act on drug precursors

Court-toxicological laboratory, the laboratory of the Health Institute,

specialised diagnostic, scientific-research

or the teaching workplace or public high school

research institution in accordance with the Act on public research institutions-$ 500



g) change the license because of the change of the responsible person, changes

first or last name of the person responsible, the change of residence or the changes

the name pursuant to the Act on drug precursors, and by directly

applicable European Union legislation governing precursors

drugs ^ 77) toxicological laboratory, laboratory Court Health Institute,

specialised diagnostic, scientific research or

workplace learning high school or public research institution

under the law on public research institutions, Czk 300



(h) the new special edition of the licences) because of a change in the particulars specified

in a special license pursuant to the Act on drug precursors, and by directly

applicable European Union legislation regulating drug precursors ^ 77)

or renewal of special license pursuant to the law on precursors

drugs and by the directly applicable European Union legislation

regulating drug precursors ^ 77) care providers-$ 300 and $ 200

for each new place of business

referred to in the application for a new

special license



I change the special license) because of a change of the responsible person, changes

first or last name of the person responsible or changes of registered office, place of residence,

name, trade name or in the name or the surname of the holder of the Special

a licence under the Act on drug precursors and by directly applicable

European Union legislation regulating drug precursors ^ 77) providers

Pharmacy-$ 300



j) issue a registration certificate to the activity with the substance

category 2 or 3 according to the law on drug precursors, and by directly

applicable European Union legislation regulating drug precursors ^ 77) EUR 3 000



k) the issue of the special registration to the activity with the substance

category 2 or 3 according to the law on drug precursors, and by directly

applicable European Union legislation regulating drug precursors ^ 77)

care providers CZK 2 000



l) issue a new certificate of registration of the activity with the substance

category 2 or 3 because of changes in registration data according to the law

on drug precursors and by the directly applicable European Union legislation

regulating drug precursors ^ 77) $ 1,000



m) issue a new certificate of special registration to activities with the

substance category 2 or 3 because of changes in registration data according to

the law on drug precursors and by directly applicable regulations

The European Union on drug precursors ^ 77) providers

Pharmacy-$ 600



n) issue of an export or import permit under the Act

on drug precursors, and by directly applicable regulations

The European Union on drug precursors ^ 77) $ 1,000



about) issue a registration certificate to the activity with a default or a helping

substance according to the law on drug precursors-$ 500



p) issue a new certificate of registration to the activity with a default

or other ingredient because of changes in registration data

under the law on drugs precursors Czk 300



Exemption



From the fee referred to in subparagraphs (j)) and k) are exempt persons registered

The Ministry of health under Act No. 167/1998 Coll., on substance abuse

substances and amending some other acts, in the version in force before the

entry into force of the Act on drug precursors.



77) European Parliament and Council Regulation (EC) No 273/2004 of 11 March.

February 2004 on drug precursors, as amended.



Council Regulation (EC) No 111/2005 of 22 December 2004. December 2004

laying down rules for the monitoring of trade in drug precursors between the

Community and third countries, as amended.



Commission Regulation (EC) No 1277/2005 of 27 June. July 2005

detailed rules for the regulation of the European Parliament and of the Council (EC)


No 273/2004 on drug precursors and for Council Regulation (EC) No 111/2005,

laying down rules for the monitoring of trade in drug precursors between the

Community and third countries, as amended. ".



PART THREE



Amendment of the Act on the police of the Czech Republic



Article. (IV)



In section 34 of Act No. 273/2008 Coll., on the police of the Czech Republic, as amended by

Act No. 150/2007 Coll., paragraph 4 reads:



"(4) If a thing referred to in paragraph 1 or 2 of the narcotic or psychotropic substance

or precursor drugs, the police such a substance after the things be destroyed or

registers for the purposes referred to in section 38, where it has been decided to forfeit of the

case or the prevents things. In a similar manner by the police in narcotics proceeds

or psychotropic substances or precursors of drugs obtained in the context of

with the work undertaken pursuant to section 69 and 70. ".



Article. In



Transitional provision



Narcotic substances, psychotropic substances or precursors that were to

the effective date of this Act, stored in the warehouses of regime

Police of the Czech Republic and which is no longer needed for further proceedings,

Police of the Czech Republic.



PART FOUR



The EFFECTIVENESS of the



Article. (VI)



This Act shall take effect on 1 January 2000. January 2014.



Němcová in r.



Zeman in r.



Samantha r in r.

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