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Top Industry News
- FDA REMS Document Technical Conformance Guide
- CDSCO Asks Companies to Submit Summaries of Their Indian Pharmacovigilance Systems
- PMDA Updated Non-Clinical Investigation Procedures for Medical Devices
- MHRA Human Medicines: Register of Electronic Export Certificates
- SWISS Updates Decentralized Clinical Trials Plan
- PMDA Methods for Submission of Data Pertaining to Compliance Review of Approval Review Data for Generic Drugs for Prescription
- ICH Releases Draft Guideline Proposing Harmonized Bioequivalence Testing
- India Calls for Medical Device Testing Laboratories to Step up to Increase Assessment Capacity