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From borderline classifications and low-risk criteria to complex substance identity and variable composition, these products require careful justification at every step. This training explores the key regulatory grey areas, including specification challenges, read-across strategies and the use of literature in place of standard data packages.
With a strong focus on applicable knowledge, the course equips you to navigate ambiguity, address common pitfalls, and build defensible IUCLID submissions for complex and often unconventional substances.
Deliverables:Step-by-step understanding of EU regulatory procedures for biocontrol
Actionable guidance on data generation and dossier compilation
Expert tips to streamline approvals and reduce regulatory delays
Sectors that should take part:
Chemical industry
Biopesticide and biocontrol developers and producers
Startups and small and medium-sized enterprises developing biocontrol products
Regulatory affairs
Professional groups:
Academic Researchers aiming to translate lab findings into regulatory submissions
Industry Experts transitioning to or supporting biocontrol solutions
Regulatory Affairs Specialist and consultants expanding into the biocontrol space
From borderline classifications and low-risk criteria to complex substance identity and variable composition, these products require careful justification at every step. This training explores the key ...
Mehr Informationen| Datum | Dauer | Preis | ||
|---|---|---|---|---|
| Online, DE | ||||
| 12.11.2026 4 h | 4 h | Details | Details Jetzt buchen | |