Top Industry News
- ANVISA Publishes Three New Guides on Drug Registration
- Malaysia’s MDA to Start Withdrawing Incomplete Medical Device Applications After 30 Days
- SWISS MDR/IVDR Amendment: Ensuring Equivalence to the EU Medical Device Regulations
- PMDA Updated Information On Humanitarian Clinical Trials (Drugs, Devices/Refurbishment)
- SFDA Specifications: Test Procedures and Acceptance Criteria for New Veterinary Drug Substances and New Medicinal Products: Chemical Substances (VICH GL39)
- FDA Identification of Medicinal Products — Implementation and Use
- PMDA Submission of Materials Related to Subcommittees, etc.
- FDA Draft Guidance Allows AI/ML Devices to Evolve Without Requiring New Submissions
- TGA Changes to Medical Device Essential Principles for Nanomaterials