Agricultural biologicals may be global. Regulatory pathways aren’t
Bringing a biological crop protection product to market requires more than a strong technical dossier. Regulatory requirements can vary significantly across the US, Canada, EU and GB, influencing development plans, data requirements and time to market.
Sagentia Regulatory, formerly TSG Consulting, helps with:
- Regulatory strategy and market access planning
- Complex biological submissions, including microbial dossiers, secondary metabolite assessments and whole genome sequencing reviews
- Product registrations, renewals and dossier development, including data gap assessments, literature reviews and regulatory submissions
Download our leaflets and insight reports
Product authorisations in Europe
Clearing the path for biological product commercialization
Key phases in the acquisition and development of a pesticide and/or biopesticide (EU)
Steps to secure EU active substance approval and renewal
Environmental sciences
Navigating EFSA’s revised birds and mammals guidance
US and Canada regulatory services