APC provides a complete service ensuring successful
product re-registration in EU Member States
APC can:
- Evaluate what uses can probably be registered according to new EU risk assessments
- Manage studies and field trials, repare, submit and follow-up dossiers
- Co-ordinate multi-company Task Forces
Cost and timeline for the Annex III dossier will depend on:
- Changes in target crops, pests, diseases and weeds
- Changes in GAP compared with pre Annex I uses
- Changes in formulation type and composition
- Individual requirements by different member states
pdf for more details