Regulation EC 1107/2009
Placing on the market of PPPs
- Regulation EC 1107/2009
- Regulation EU 540/2011 - approved substances [Updated 03/09/2014]
- Regulation EU 546/2011 - uniform principles for evaluation and authorisation of PPPs
- Regulation EU 547/2011 - labelling requirements for PPPs
- Regulation EU 283/2013 - setting data requirements for active substances
- Communication - list of test methods and guidance documents
- Regulation EU 284/2013 – setting data requirements for PPPs
- Communication - list of test methods and guidance documents
- Report on minor uses (Art. 51)
- Questions and answers - Rev 6 [Updated 31/03/2022 - under revision]
Adoption of Regulation EC 1107/2009
Directive 91/414/EEC
Evaluation, authorisation, approval of active substances at EU-level and national authorisations of PPPs
- Directive 91/414/EEC
- Regulation EC 33/2008 - implementation rules of Directive 91/414/EEC – regular and accelerated procedure for the assessment of active substances
- Resubmitted applications of active substances NOT in Annex I
- Regulation EC 1095/2007 - implementation rules of Directive 91/414/EEC
- Stages 1, 2, 3 and 4 of the programme of work for the examination of the active substances
Regulation EEC 3600/92 - implementation of the first stage
Regulation EC 451/2000 - implementation of the second stage
Regulation EC 1490/2002 - implementation of the third stage
Regulation EC 2229/2004 - implementation of the fourth stage - Regulation EU No 188/2011 - procedure for the assessment of active substances which were not on the market (new active substances)
Information to stakeholders
Phosphonate products
- Letter to stakeholders: Trade problems due to phosphonate residues in certain food products
- Phosphonate products on Phytoweb – Information by the Belgian Federal Public Service Health, Food Chain Safety and Environment
Related links
- Competent authorities – contact points
- Applicable penalties in the different Member States under Article 72 of Regulation (EC) 1107/2009