Our Life science resources & articles | ProductLife Group

French Pharmacovigilance Survey: Addressing a Potential Request from Competent Authority

China Takes Steps to Assist Drug-Device Submission Process with New Guideline

Regulating Biotech Products in the Complex LATAM Region

Placing Renewed Focus on Risk Management and the RMP

Preparing for the EU’s New, More Harmonized, Clinical Trials Portal

Adopting a Strategic Approach to Managing EU Variations

France introduces new early access program for pressing patient need

Electronic Product Information (ePI)

Artificial Intelligence (AI) in Pharmacovigilance: do we really need it…?

Load more resources