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

EventHumanMedicinesQuality of medicinesScientific guidelines

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Date

, -

Lokacija

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.

Documents

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