Top Industry News
- SWISS Adjustments to the Guidelines for Medicinal Product Information for Medicinal Products for Human Use
- Europe Notified Bodies Create Best Practice Guide for Submitting IVDR Technical Documents
- Malaysia’s MDA Creates Online Payment System for Medical Device Regulatory Services
- SWISS New Guidelines on Mobile Technologies for Human and Veterinary Medicinal Products
- MHRA Human Medicines: Register of Electronic Export Certificates
- Pakistan DRAP Seeks Feedback on Planned Changes to Drug Research Regulations
- FDA Q13 Continuous Manufacturing of Drug Substances and Drug Products
Mergers & Acquisitions
- How to Determine a Predicate Device for your 510(k) Medical Device?
- The Importance of Regulatory Strategy in Medical Devices
- PMS Management of Medical Devices and IVDs in the European Union (EU)
- How are Near-patient Testing Devices Regulated under EU IVDR?
- FSSAI Releases Regulatory Standards for Basmati Rice Effective August 01, 2023
- Digital Transformation in Pharmacovigilance (PV)