Directive 1998/8 - Placing of biocidal products on the market

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1.

Current status

This directive was in effect from May 14, 1998 until August 31, 2013 and should have been implemented in national regulation on May 13, 2000 at the latest.

2.

Key information

official title

Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market
 
Legal instrument Directive
Number legal act Directive 1998/8
Original proposal COM(1993)351 EN
CELEX number i 31998L0008

3.

Key dates

Document 16-02-1998
Publication in Official Journal 24-04-1998; Special edition in Latvian: Chapter 03 Volume 023,Special edition in Estonian: Chapter 03 Volume 023,Special edition in Polish: Chapter 03 Volume 023,Special edition in Maltese: Chapter 03 Volume 023,Special edition in Croatian: Chapter 03 Volume 001,Special edition in Slovenian: Chapter 03 Volume 023,Special edition in Czech: Chapter 03 Volume 023,Special edition in Slovak: Chapter 03 Volume 023,Special edition in Romanian: Chapter 03 Volume 024,Special edition in Bulgarian: Chapter 03 Volume 024,Special edition in Hungarian: Chapter 03 Volume 023,Special edition in Lithuanian: Chapter 03 Volume 023,OJ L 123, 24.4.1998
Effect 14-05-1998; Entry into force Date pub. + 20 See Art 35
End of validity 31-08-2013; Repealed by 32012R0528
Transposition 13-05-2000; At the latest See Art 34

4.

Legislative text

24.4.1998   

EN

Official Journal of the European Communities

L 123/1

 

DIRECTIVE 98/8/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

of 16 February 1998

concerning the placing of biocidal products on the market

THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION,

Having regard to the Treaty establishing the European Community, and in particular Article 100a thereof,

Having regard to the proposal from the Commission (1),

Having regard to the opinion of the Economic and Social Committee (2),

Acting in accordance with the procedure laid down in Article 189b of the Treaty (3) in the light of the joint text approved on 16 December 1997 by the Conciliation Committee,

 

(1)

Whereas, in their resolution of 1 February 1993 on a Community programme of policy and action in relation to the environment and sustainable development (4), the Council and the representatives of the Governments of the Member States, meeting within the Council, approved the general approach and strategy of the programme presented by the Commission, in which the need for risk management of non-agricultural pesticides is emphasised;

 

(2)

Whereas, both when the eighth Amendment (5) to Council Directive 76/769/EEC of 27 July 1976, on the approximation of the laws, regulations and administrative provisions of the Member States relating to restrictions on the marketing and use of dangerous substances and preparations (6) was adopted in 1989 and during the discussion in the Council on Directive 91/414/EEC concerning the placing of plant protection products on the market (7), the Council expressed concern at the lack of harmonised Community provisions for biocides, formerly known as non-agricultural pesticides, and invited the Commission to examine the situation in Member States and the possibility for action at Community level;

 

(3)

Whereas biocidal products are necessary for the control of organisms that are harmful to human or animal health and for the control of organisms that cause damage to natural or manufactured products; whereas biocidal products can pose risks to humans, animals and the environment in a variety of ways due to their intrinsic properties and associated use patterns;

 

(4)

Whereas the Commission review showed differences in the regulatory situation in the Member States; whereas such differences may constitute barriers not only to trade in biocidal products but also to trade in products treated with them, thereby affecting the functioning of the internal market; whereas, therefore, the Commission proposed the development of a framework of rules relating to the placing on the market for use of biocidal products, taking as a condition a high level of protection for humans, animals and the environment; whereas, having regard to the principle of subsidiarity, decisions taken at Community level should be restricted to those necessary for the proper functioning of the common market and to avoid duplication of work by Member States; whereas a directive on biocidal products is the most appropriate way of establishing such a framework;

 

(5)

Whereas the framework of rules should provide that biocidal products should not be placed on the market for use unless they have complied with the relevant procedures of this Directive;

 

(6)

Whereas, to take account of the specific nature of some biocidal products and the risks associated with their proposed use, it is appropriate to provide for simplified authorisation procedures, including registration;

 

(7)

Whereas it is appropriate that the applicant submit dossiers which contain information which is necessary to evaluate the risks that will arise from proposed uses of the product; whereas a common core data set for active substances and for biocidal products in which they are contained is necessary so as...


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Original proposal

 

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