Industry stakeholder webinar on revised environmental risk assessment guideline for medicinal products for human use - 1 year experience

Event Human Medicines Quality of medicines Scientific guidelines

Date

, -

Location

Online
European Medicines Agency, Amsterdam, the Netherlands

Event summary

The guideline on the environmental risk assessment of medicinal products for human use has been revised and came into force in September 2024. 

Stakeholders from industry (originator companies, generic companies, CROs) are invited to join this webinar on the one year experience with the revised guideline.

Webinar participation

Webinar participation is via Webex:

You do not need to register to follow the webinar. Please feel free to share the above Webex link with others.

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