Top Industry News
- MHRA Guidance on Qualified Person Responsible for Pharmacovigilance (QPPV) Including Pharmacovigilance System Master Files (PSMF)
- PMDA We Have Updated the Page of GMP Compliance Inspection Services
- MHRA Register Medical Devices to Place on the Market
- India Plans Regulatory Streamlining to Promote Medical Device Industry
- TGA Revises MDR Transition Strategy to Reflect New EU Timeline
- ANVISA Understand the New Rules for Clinical Analysis Laboratories
- MHRA Notify the MHRA About a Clinical Investigation for a Medical Device
- Philippine FDA Adopts Updated WHO Guidelines On the Evaluation of Biosimilars
- MHRA Impact of Extension of Medical Device Regulations Transitional Period and the Validity of Certificates in the EU
- ANVISA Advises on Importing Medical Devices for Repair or Repair