Achieving the Regulatory GRAS Status with Optimal Review of Safety & Data Generation
Time: 9:00 am
day: Pre-Conference Day
Details:
The journey to regulatory approval can sometimes seem like a never-ending and complex labyrinth. Cross-departmental collaboration with regulatory decision makers will help you bridge this gap and help exercise the skills that are in your control.
Join this workshop to unite with industry-leading regulatory experts to understand the ins and outs of pre-submission meetings and regulatory frameworks to streamline approval.
This workshop will gather experts to discuss:
- Outlining and assessing GRAS notices to help inform review of safety and identify early market opportunities for specific bioactives
- Pin-pointing nuances in data quality to best prepare for pre-submission meetings and effectively demonstrate growth and intake outcomes
- Implementing risk-benefit models for regulatory strategies to compare alternatives and hone in on best directions forward
