DEVREG services on development are focused on the management and monitoring of development programs in Europe, in collaboration with different CROs and laboratories, to provide a consistent data package for registration of agrochemicals in Europe.
DEVREG offers a complete service on field trials coordination assisting the Client Development Manager in trial planning and executes the set-up and documentation of trial protocols for any GEP field efficacy trials as well as for GLP-study plans (residues).
DEVREG offers the assistance for contracting trials and follow-up with external CROs regarding trial progress, data capture and reporting. DEVREG also supports Client Development Manager as a second interface for any trial related activities towards Regulatory, Stewardship or Research groups.
Regulatory areas:
- Physico Chemical properties and stability.
- Analytical methods (validations, ILV, etc.).
- Efficacy, crop safety, processing, yield, etc.
- Toxicological studies and non-dietary exposure.
- Residues on plant product and processed commodities.
- Ecotoxicological studies
Development coordination activities include:
- Trial planning under direction of the Client Development Manager.
- Trial supervision and reporting, summarizing and initial data interpretation.
- Work with regulatory group in the establishment of GEP and GLP-study plans for field trials and ensuring that all necessary data capture is reflected in the trial protocol.
- Assist Development Managers in coordinating efforts with Regulatory, Stewardship and Research groups.
- Review of service provider contracts for adherence to administrative and operational procedures.
- Assist with updating of planning records and trials status to Development Manager.
For further information, please contact with our Management and staff to provide the best proposal for development of your products.