# Commission Regulation (EC) No 1490/2002 of 14 August 2002 laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and amending Regulation (EC) No 451/2000 (Text with EEA relevance) (revoked)

EU Regulation No 1490/2002 · adopted 14 August 2002

Commission Regulation (EC) No 1490/2002 of 14 August 2002 laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and amending Regulation (EC) No 451/2000 (Text with EEA relevance)

## Introductory text

Commission Regulation (EC) No 1490/2002
of 14 August 2002
laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and amending Regulation (EC) No 451/2000
(Text with EEA relevance) (revoked)
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## 1 Subject matter and scope

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## 2 Definitions

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## 3 Member State authority

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## 4 Measures in case of imbalances

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## 5 Withdrawal or replacement of notifier

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## 6 Submission and checking of data lists

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## 7 Submission of dossiers

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## 8 Submission of information by third parties

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## 9 Completeness check of dossiers

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## 10 Evaluation by the rapporteur Member State

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## 11 Receipt of and access to the draft assessment report

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## 11a Examination of the draft assessment report

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## 11b Active substance with clear indications that they do not have any harmful effects

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## 11c Consultation of the EFSA

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## 11d Submission of additional information after the draft assessment report has been submitted to the EFSA

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## 11e Withdrawal by notifier

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## 11f Active substance for which there are clear indications of harmful effects

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## 12 Presentation of a draft directive or draft decision

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## 12a View by the EFSA

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## 13 Finalised review report

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## 14 Suspension of time limits

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## 15 Measures taken by Member States

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## 16 Interim progress report

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## 17 Fees

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## 18 Other charges, taxes, levies or fees

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## 19 Temporary measures

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## 20 Amendment to Regulation (EC) No 451/2000

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## 21 Entry into force

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## Signature

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## Annex I: List of active substances (column A), rapporteur Member States (column B) and notifying producers (code identification) (column C)

## A 

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## B 

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## Annex II List of notifiers' code identification, names and addresses

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## Annex III: Coordinating authority in the Member States (more details are available at the following website: http://www.europa.eu.int/comm/food/fs/ph_ps/pro/index_en.htm)

## AUSTRIA

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## BELGIUM

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## DENMARK

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## GERMANY

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## GREECE

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## SPAIN

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## FINLAND

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## FRANCE

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## IRELAND

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## ITALY

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## LUXEMBOURG

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## NETHERLANDS

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## PORTUGAL

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## SWEDEN

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## UNITED KINGDOM

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## Annex IV: Organisations in the Member States to be contacted concerning further details on the payment of the fees referred to in Article 17 and to which such fees have to be paid

## AUSTRIA

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## BELGIUM

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## DENMARK

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## GERMANY

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## GREECE

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## SPAIN

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## FINLAND

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## FRANCE

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## IRELAND

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## ITALY

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## LUXEMBOURG

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## THE NETHERLANDS

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## PORTUGAL

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## SWEDEN

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## UNITED KINGDOM

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## Annex V Criteria for clear indications of no harmful effects

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## 1 

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## 2 

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## Annex VI Criteria for clear indications of harmful effects

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## 1 

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## 2 

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Source: https://www.legislation.gov.uk/eur/2002/1490 (the official version)
Page: https://openlegislation.uk/eu-regulation-2002-1490
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.