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Title
Regulatory Rapporteur June 2022
Summary
Pharmacovigilance legislation - Exploring the impact of pharmacovigilance legislation on human medicines Plus: Interview: Updates to quality legislation from the EMA Article: Medical device standards update Interview: Evolutions in patient healthcare at the MHRA Article: Exploring Amgen's Project Orbis experience with sotorasib Article: What can past decision-making data tell us about how the FDA will make future combination product categorisation decisions?
DocumentAccess
Regulatory Rapporteur June 2022MEMBERS
What can past decision-making data tell us about how the FDA will make future combination product categorisation decisions?MEMBERS
Updates to quality legislation from the EMAMEMBERS
Medical device standards updateMEMBERS
Evolutions in patient healthcare at the MHRAMEMBERS
10 years of pharmacovigilance legislation: the perspective of a national agencyMEMBERS
Exploring Amgen's Project Orbis Experience with sotorasibMEMBERS
How regulators are navigating the evolving pharmacovigilance landscape PUBLIC