Cabinet of Ministers Regulation No 1135 in 2013 (22 October. No 55 70) amendments to the Cabinet of Ministers of 8 March 2005, regulations No 175 "prescription form manufacturing and storage, as well as prescription and storage rules" Issued in accordance with article 60 of the law on medical treatment and the law "on the illicit manufacture of narcotic drugs and psychotropic substances and to the legitimate movement of medicinal products order" 36. the first paragraph of article 1 do cabinet 8 March 2005 rules no 175 "prescription form of manufacture and storage as well as prescription and storage rules "(Latvian journal, 2005, nr. 48; 2007, 104 no; 2008, 22, nr. 87; 2011, 60 no) the following amendments: 1. replace the text, the word" Centre "(the fold) with the word" service "(the fold) (except this rule 7 and 34 and 50.2); 1.2. to replace the words "in the text of the provisions of the form" E "E or S form"; 1.3. make point 7 by the following: "7. Prescription forms of treatment of treatment institutions and persons distributed by the national health service (hereinafter service). Service in accordance with the legislation on public procurement organized order prescription form, as well as for the manufacture of a prescription form of commercial printing, 5 and 6 of these regulations, paragraph defensive incorporated to prevent the prescription form of counterfeiting. " 1.4. to supplement 16 to the third sentence by the following: "the wallet may not be equipped with an alarm if it is equipped with an alarm in the room that provides permanent signalling connection."; 1.5. to Supplement 26 to the third sentence by the following: "the European Union, the countries of the European economic area or the Swiss Confederation at the prescription pharmacy stores in three years. '; 1.6. to replace the first sentence of paragraph 48, the number "30" with the number "90"; 1.7. to express in this paragraph 50.2: "50.2. the Ministry of health, State Agency of medicines, health inspection and law enforcement institutions to request information on the medicines and medical equipment, drawn to the consumer the specific prescription forms;" 1.8. to supplement the rules with 57 and 58 as follows: ' 57. Prescription forms, printed up to 2013 of 25 October, authorized to distribute up to July 1, 2014. 58. Write out the drugs and medical devices on the prescription form, printed in up to 25 October 2013, 2014 allowed December 31. From January 1, 2014, when drugs and medical devices in these forms: the word "(ls)". "; 1.9. to supplement the rules with the informative reference to European Union directives as follows: "Informative reference to European Union Directive provisions included in the law arising from the Commission of 20 December 2012, the implementation of the directive in 2012/52/EU, laying down measures to facilitate the prescriptions issued in another Member State."; 1.10. Express 1 and 2 of the annex by the following: "1. the annex to Cabinet of Ministers of 8 March 2005, regulations No 175 regular recipes model form Annex 2 of the Cabinet of Ministers of 8 March 2005, regulations No 175 recipes Special model form" 1.11. Express 3.2.2 the first sentence as follows: "the patient's first name, last name (indicating the full name, without using the initials), personal code (E or S bearer form – identification number) by address or telephone. "; 1.12. Express 3.2.4. subparagraph by the following: "the treatment of 2.4 persons first name, last name (indicating the full name, without using the initials), specialty and personal number or health inspections of the assigned treatment person's identifier statement."; 1.13. Express 3. paragraph 12 of the annex as follows: ' 12. If the medicinal product is prohibited from replacing the medical person cross out the words "medicinal product authorised for replace" and indicate the reasons for the ban. Justification the references you can use recipes to follow-up the second half, using the designation "Vertu". "; 1.14. the supplement to annex 3, paragraph 21, after the words "national compensation" with the words "category or"; 1.15. the supplement to annex 3, chapter IV, of the following: "(IV). the additional requirements of a prescription form to fill out, if the patient is informed that the recipe will be used in one of the European Union, the countries of the European economic area or the Swiss Confederation 24. Information about the patient to indicate the patient's date of birth. 25. the content of the treatment the person specifies additional properties (e-mail address and telephone or fax number (with country code)). 26. Prescribing medicine, indicates one of the following names: 26.1. drug international non-proprietary name, or, if such name does not exist, the General name of the medicinal product; 26.2. the manufacturer of the medicinal product, the name if the medicinal product is prohibited from replacing, deleting the words "medicinal product authorised for replace" and stating the reasons for the ban; 26.3. the manufacturer of the medicinal product name if the extract biological medicinal products. " 2. the rules shall enter into force on 25 October 2013. Prime Minister Valdis Dombrovskis Health Minister Ingrida Cricket»