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Third Amendment Of The Biocides Act Gebührentarifv Ii.

Original Language Title: Dritte Änderung der BiozidG-GebührentarifV II

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209. Regulation of the Federal Minister for Agriculture, Forestry, Environment and Water Management, with which the Biocides-G-fee tariff V II is amended for the third time

On the basis of § 41 of the Biocidal Products Act (Biocides Act), BGBl. No 105/2000, in the version of the Federal Law BGBl. I No 151/2004, shall be ordered:

The Biocides-G-fee tariff V II, BGBl. II No 331/2003, as amended by the BGBl Regulation. II No 352/2008, shall be amended as follows:

1. In Section 1 (1), at the end of Z 9, the word shall be: "or" The following Z 10 shall be inserted:

" 10.

for the approval of an experiment or test in accordance with § 7 (2) to (4) Biocide G, in which a release into the environment is foreseen or expected "

2. In § 1 para. 2, at the end of the Z 9 the point is given by the word "or" , the following Z 10 shall be added:

" 10.

the approval of an experiment or test in accordance with Section 7 (2) to (4) Biocide G, in which a release into the environment is foreseen or expected. "

(3) Sections I, I A, I B, I C, II, II A, II B, II C, III and III A of the Annex are:

" Section I

Application for authorisation of a biocidal product according to § 11 para. 1 Biocides G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

1.0

Collection, documentation and administration of the application including the documents

180,-

VPG

2.0

Performance of the completeness check, including the examination of additional data in accordance with Annex IIIB to Directive 98 /8/EC for a product type according to the Appendix to § 2 para. 1 Z 4 Biocides G

1 760.-

VPG

3.0

Implementation of the completeness check, for a product type (as far as not falling under the tariff post 2.0)

1 540,-

VPG

4.0

Additional implementation of the completeness check for each additional product type, in addition to tariff post 2.0 or 3.0

165,-

BG

5.0

Assessment of the particulars and documents, including the evaluation of additional data in accordance with Annex IIIB to Directive 98 /8/EC as regards the requirements for the admission requirements in accordance with Article 11 (1) of the Biocides Act, for the first type of product according to the Appendix. § 2 para. 1 Z 4 Biocide G, if the biocidal product contains an active substance

14 300,-

BG

6.0

Evaluation of the information and documents relating to the requirements of the admission requirements in accordance with § 11 paragraph 1 Biocides G, for the first product type (if not falling within the tariff post 5.0), if the biocidal product contains an active substance

13 200,-

BG

6.1

evaluation of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions in which the active substance is listed in Annex I to Directive 98 /8/EC or a modification or supplement to the specific provisions of Annex I to Directive 98 /8/EC, or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, a maximum value or a number of maximum residue limits (MRLs), or to modify existing MRLs, for a product type as set out in section 2 (1) (4) of the Biocidal Products Act, if the biocidal product contains an active substance, if appropriate in addition to Tariff post 5.0 or, if applicable, 6.0

30 000,-

BG

6.2

evaluation of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions in which the active substance is listed in Annex I to Directive 98 /8/EC or a modification or supplement to the specific provisions of Annex I to Directive 98 /8/EC, or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required for a product type according to the Appendix to § 2 para. 1 Z 4 Biocides G, if the biocidal product contains an active substance, if necessary in addition to the tariff post 5.0 or, if applicable, 6.0

20 000,-

BG

6.3

evaluation of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions in which the active substance is listed in Annex I to Directive 98 /8/EC or a modification or supplement to the specific provisions of Annex I to Directive 98 /8/EC, or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required for a product type according to the Appendix to § 2 para. 1 Z 4 Biocides G, if the biocidal product contains an active substance, if necessary in addition to the tariff post 5.0 or, if applicable, 6.0

10 000,-

BG

7.0

Evaluation of the particulars and documents relating to the requirements of the admission requirements in accordance with § 11 paragraph 1 Biocides G, in addition to the tariff post 5.0 or 6.0, for each additional product type for which the evaluation of additional data according to Annex IIIB of the Directive 98 /8/EC is necessary

2 000,-

BG

7.1

evaluation of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions in which the active substance is listed in Annex I to Directive 98 /8/EC or a modification or supplement to the specific provisions of Annex I to Directive 98 /8/EC, or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, a maximum value or a set of maximum residue limits (MRLs), or to modify existing MRLs, per additional product type, if appropriate in addition to the tariff post 7.0

3 000,-

BG

7.2

evaluation of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions in which the active substance is listed in Annex I to Directive 98 /8/EC or a modification or supplement to the specific provisions of Annex I to Directive 98 /8/EC, or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC is required, pro more Product type, if necessary in addition to tariff post 7.0

2 000,-

BG

8.0

Evaluation of the information and documents with regard to the requirements of the admission requirements in accordance with § 11 para. 1 Biocides G (as far as not falling under the tariff post 7.0), in addition to tariff post 5.0 or 6.0, per additional product type

1 000,-

BG

9.0

Evaluation of the particulars and documents relating to the application of the admission requirements in accordance with § 11 paragraph 1 Biocides G, in addition to the tariff post 5.0 or 6.0, per additional active substance from Annex I or IA to Directive 98 /8/EC

3 300,-

BG

9.1

Assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if a modification or addition to the specific provisions under which the further active substance is listed in Annex I to Directive 98 /8/EC or a modification or completion of the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, and on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, To establish the maximum or several residue limits (MRLs) or to modify existing MRLs, for a product type as set out in the Appendix to § 2 (1) Z 4 Biocides G, per further active substance from Annex I or IA to Directive 98 /8/EC, In addition to the tariff post 9.0

30 000,-

BG

9.2

Assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if a modification or addition to the specific provisions under which the further active substance is listed in Annex I to Directive 98 /8/EC or a modification or completion of the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, and on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required for: Product-type according to the Appendix to § 2 para. 1 Z 4 Biocides G, per further active substance from Annex I or IA to Directive 98 /8/EC, if appropriate in addition to the tariff post 9.0

20 000,-

BG

9.3

Assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if a modification or addition to the specific provisions under which the further active substance is listed in Annex I to Directive 98 /8/EC or a modification or completion of the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or annex IIIA, point XII and/or point XIII of Directive 98 /8/EC is required for a Product-type according to the Appendix to § 2 para. 1 Z 4 Biocides G, per further active substance from Annex I or IA to Directive 98 /8/EC, if appropriate in addition to the tariff post 9.0

10 000,-

BG

10.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. a Biocides

750,-

BG

11.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. b Biocides

2 000,-

BG

12.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. c Biocides

4 000,-

Section I A

Application for authorisation of a biocidal product according to § 11 paragraph 1 Biocides G, which is already provisionally authorised pursuant to § 12 para. 1 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

BG

13.0

Evaluation of the information and documents with regard to the requirements of the admission requirements in accordance with § 11 paragraph 1 Biocides

1 100,-

Section I B

Application for authorisation of a biocidal product in the form of mutual recognition according to § 13 Biocide-G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

14.0

Collection, documentation and administration of the application including the documents

180,-

VPG

15.0

Implementation of the completeness check

850,-

BG

16.0

Evaluation of the information and documents relating to the requirements of the admission requirements in accordance with § 13 Biocide G,

3 300,-

BG

17.0

Evaluation of the information and documents with regard to the requirements of the admission requirements in accordance with § 13 Biocides G, if the requirement for documents according to § 13 para. 3 Biocide G is required, in addition to the tariff post 16

3 300,-

Section I C

Application for authorisation of a biocidal product within a defined frame formulation according to § 15 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

18.0

Collection, documentation and administration of the application including the documents

100,-

VPG

19.0

Implementation of the completeness check

250,-

BG

20.0

Evaluation of the information and documents with regard to the requirements of the admission requirements in accordance with § 15 Biocides

750,-

Section II

Application for registration of a biocidal product pursuant to § 11 para. 2 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

21.0

Collection, documentation and administration of the application including the documents

110,-

VPG

22.0

Implementation of the completeness check

550,-

BG

23.0

Evaluation of the information and documents relating to the requirements of the registration requirements in accordance with § 11 paragraph 2 Biocides G, for the first product type if the biocidal product contains an active substance

5 500,-

BG

23.1

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, a maximum value or a number of maximum residue limits (MRLs), or to modify existing MRLs, for a product type as set out in section 2 (1) (4) of the Biocidal Products Act, if the biocidal product contains an active substance, if appropriate in addition to Tariff post 23.0

10 000,-

BG

23.2

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required for a product type according to the Appendix to § 2 para. 1 Z 4 Biocide G, if the biocidal product contains an active substance, if necessary in addition to the tariff post 23.0

6 500,-

BG

23.3

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required for a product type according to the Appendix to § 2 para. 1 Z 4 Biocide G, if the biocidal product contains an active substance, if necessary in addition to the tariff post 23.0

3 500,-

BG

24.0

Evaluation of the information and documents with regard to the requirements of the registration requirements in accordance with § 11 paragraph 2 Biocide G, in addition to the tariff post 23.0, per additional product type

550,-

BG

24.1

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, a maximum value or a number of maximum residue limits (MRLs) or to modify existing MRLs if the biocidal product contains an active substance, per additional product type, if appropriate in addition to the subheading 24.0

750,-

BG

24.2

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC shall be required if: Biocidal product contains an active substance, per additional product type, if appropriate in addition to the tariff post 24.0

500,-

BG

25.0

Evaluation of the information and documents with regard to the requirements of the registration requirements in accordance with § 11 paragraph 2 Biocides G, in addition to the tariff post 23.0, per further active substance from Annex IA to Directive 98 /8/EC

1 375,-

BG

25.1

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or Annex IIIA, point VI, and additional proof required in accordance with Annex IIA, point VII and/or Annex IIIA, in accordance with Annex IIA, Point XII and/or XIII of Directive 98 /8/EC is required and, where appropriate, a maximum value or a number of maximum residue limits (MRLs), or to modify existing MRLs, per further active substance from Annex IA to Directive 98 /8/EC, where appropriate in addition to the subheading 25.0

10 000,-

BG

25.2

the assessment of the particulars and documents referred to in Annex IIA and IIIA of Directive 98 /8/EC, if any modification or addition to the specific provisions under which the active substance is listed in Annex IA to Directive 98 /8/EC or a modification or a supplement to the assessment report on the basis of additional required audit evidence in accordance with Annex IIA, point VI and/or in accordance with Annex IIIA, point VI, or on the basis of additional required audit evidence in accordance with Annex IIA, point VII and/or Annex IIIA, Point XII and/or point XIII of Directive 98 /8/EC is required, per further Active substance from Annex IA to Directive 98 /8/EC, where appropriate in addition to the tariff post 25.0

6 500,-

BG

26.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. a Biocides

300,-

BG

27.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. b Biocides

800,-

BG

28.0

Evaluation of the information and documents relating to the provision of the conditions for the establishment of a frame formulation according to § 10 paragraph 3 Biocides G, for deviations according to § 2 para. 1 Z 10 lit. c Biocides

1 600,-

Section II A

Application for registration of a biocidal product according to § 11 paragraph 2 Biocides G, which has already been provisionally registered pursuant to § 12 paragraph 2 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

BG

29.0

Evaluation of the information and documents with regard to the requirements of the registration requirements pursuant to § 11 paragraph 2 Biocide G

500,-

Section II B

Application for registration of a biocidal product in the form of mutual recognition according to § 14 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

30.0

Collection, documentation and administration of the application including the documents

110,-

VPG

31.0

Implementation of the completeness check

275,-

BG

32.0

Evaluation of the information and documents with regard to the requirements of the registration requirements in accordance with § 14 Biocides G

1 375,-

Section II C

Application for registration of a biocidal product within a defined frame formulation according to § 15 Biocide G 1

Type of charge

Rate post

Official activity

Fee in Euro

GG

33.0

Collection, documentation and administration of the application including the documents

50,-

VPG

34.0

Implementation of the completeness check

100,-

BG

35.0

Evaluation of the information and documents with regard to the requirements of the registration requirements pursuant to § 15 Biocides

350,-

Section III

Application for authorisation of a biocidal product in case of danger in default according to § 16 Biocide G 2

Type of charge

Rate post

Official activity

Fee in Euro

GG

36.0

Collection, documentation and administration of the application including the documents

180,-

VPG

37.0

Implementation of the completeness check

1 100,-

BG

38.0

Evaluation of the information and documents with regard to the presence of the admission requirements in accordance with § 16 Biocide G (an assessment of the active substance, if necessary, is not included)

10 000,-

Section III A

Application for registration of a biocidal product in case of danger in default according to § 16 Biocide G 2

Type of charge

Rate post

Official activity

Fee in Euro

GG

39.0

Collection, documentation and administration of the application including the documents

110,-

VPG

40.0

Implementation of the completeness check

450,-

BG

41.0

Evaluation of the information and documents with regard to the presence of the registration requirements in accordance with § 16 Biocides G (a necessary assessment of the active substance if necessary is not included)

5 000,-

"

4. In the Annex, the following section VI shall be added in accordance with Section V A:

" Section VI

Application for approval of an experiment or test for research and development purposes with release of a biocidal active substance or a biocidal product into the environment according to § 7 (2) to (4) Biocide G

Type of charge

Rate post

Official activity

Fee in Euro

BG

72.0

Evaluation of the data and documents relating to the experiment or test with regard to the requirements of the approval requirements in accordance with § 7 para. 2 to 4 Biocide G

2 500,-

"

Berlakovich