Environmental Risk Assessment of Medicinal Products Requirements and Implications of the New EMA Guideline
Free Webinar
Join our expert for a focused session on navigating ERA requirements and implication of the latest EMA guideline.
📆Date: 30th September 2026
🕐 Time: 2:30 PM UTC+1 | Duration: 45 min
💻 Platform: Microsoft Teams
Webinar Overview
Are you prepared for the EMA Environmental Risk Assessment (ERA) requirements? This live webinar will provide a overview of ERA and PBT assessment, helping professionals navigate the latest regulatory expectations.
Key Learning Outcomes
Participants will be able to:
- Address the requirements of the new EMA guideline on Environmental Risk Assessment.
- Provide a comprehensive overview of environmental risk assessment and the evaluation of persistence, bioaccumulation, and toxicity (PBT) potential.
Programme Content
- Legal framework;
- Environmental Risk Assessment and PBT potential:
- Assessment phases;
- Use of environmental data previously generated by other marketing authorization holders;
- Environmental studies required for the determination of environmental risk and PBT potential.
Registration
To secure your participation, please complete the registration form.