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Top Industry News
- Great Britain Plans to Accept European CE Marks Until 2030 Under New Proposals
- ANVISA Updates the Rule Governing Requirements for Clinical Analysis Exams
- EMA Review Of Transparency Rules for the EU Clinical Trials Information System (CTIS)
- Japan’s PMDA Adds Video On Sharing Safety Risk Information to e-learning Platform
- FDA Updated Final Guidance for Industry Entitled “Q9(R1) Quality Risk Management”
- MHRA Human Medicines: Register Of Electronic Export Certificates
- FDA Draft Guidance on Decentralized Clinical Trials for Drugs, Biological Products, and Devices
- Philippine FDA Shares Guidelines on Training Sessions as face-to-face Events Resume