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11. 3.

98 EN Official Journal of the European Communities C 76/53

(98/C 76/135) WRITTEN QUESTION E-1761/97


by Jan Mulder (ELDR) to the Commission
(27 May 1997)

Subject: Use of biological crop protection products in the European Union

1. Does the Commission agree that the use of biological crop protection products should be encouraged, from
the environmental point of view and from the point of view of consumers? In this connection can the
Commission state how many biological and how many chemical crop protection products have been registered
since July 1993?

2. Does the Commission take the view that the existing directive for the registration of biological crop
protection products based on bacteria, viruses and other micro-organisms can adequately satisfy the
requirements of the market and, in particular, that such products are rapid and cost the same as comparable
chemical products?

3. If the Commission believes that this is not the case, what action is it considering in order to facilitate the use
of biological products in the future?

4. Is the Commission of the opinion that from the economic point of view the systems for registering
biological crop protection products in the European Union and in the United States are broadly comparable, and
that the two trading organizations provide their businesses with the same encouragement to take part in
international competition? If not, what action is the Commission considering to improve the competitive position
of European businesses?

Answer given by Mr Fischler on behalf of the Commission


(16 July 1997)

1. The use and authorization of plant protection products is regulated by Council Directive 91/414/EEC of
15 July 1991 concerning the placing of plant protection products on the market (1). This Directive provides a
Community decision for both chemical substances and micro-organisms (inclusion in a positive list) used in
plant protection products and for national authorizations of the preparations containing them. In principle the
criteria for both chemical substances and micro-organisms are the same, i.e. the use of the preparation and
residues resulting may not have, in accordance with the envisaged conditions of use, any harmful effects on
human or animal health or on groundwater or any unacceptable influence on the environment.

Since July 1993, 18 dossiers for chemical active substances and 3 dossiers for micro-organisms have been
accepted as complete at Community level. A final decision for inclusion in the positive list can only be taken
after a detailed evaluation on the basis of a report prepared by a Member State. Currently no chemical active
substance nor micro-organism has been included in the positive list, as the examination procedures are still
ongoing.

2. to 4. The requirements for the dossier to be submitted are different for chemical and microbial preparations.
The data requirements for microbial preparations have so far only been established in general terms. Moreover,
the Directive provides a certain flexibility when the applicant can justify that certain studies are not necessary to
demonstrate that for particular aspects human health or the environment are not at risk. The costs for the
preparation of a dossier for micro-organisms are normally lower than for chemical preparations but, in cases
where there is reason for concern, costly testing may be required to demonstrate the absence of any harmful
effects.

The Commission is currently preparing a working document in order to establish in detail the data requirements
for micro-organisms. This document will be discussed in the framework of the Organization for economic
cooperation and development (OECD) in order to establish harmonised data requirements for micro-organisms
in all OECD coutries.

Moreover the Commission is considering whether to propose a fast track procedure for the authorization of
certain low risk plant protection products, including biological plant protection products.

(1) OJ L 230, 19.8.1991.