Top Industry News
- Europe’s MDCG updated guidance on legacy medical devices, repackaging
- FDA - Data Standards for Drug and Biological Product Submissions Containing Real-World Data
- FDA-Guidance for Preparation of Food Contact Substance Notifications
- EU - EC updates Clinical Trial Regulation Q&As ahead of January go-live
- Pakistan finalizes overhaul of regulation of contract manufacturing organizations
- FDA Approves Cyltezo, the First Interchangeable Biosimilar to Humira
- FDA says IRB review still needed for IVD studies involving human specimens