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EMA draft framework of collaboration with academia
Scientific guidance on post-authorisation efficacy studies
The General Data Protection Regulation and use of health data_ challenges for pharmaceutical regulation
ENCePP Seal studies and imposed PASS_ new compliance and disclosure measures
EMA patient registries initiative
Table of effects in benefit-risk assessments
Promoting ENCePP at national level - Introduction to the Italian model
Perspective from CROs
Perspective from industry
Perspective from academia