Top Industry News
- PMDA FY2023 Pharmaceutical and Medical Device Safety Information (No.400-)
- FDA - Real Time Oncology Review (RTOR) Guidance for Industry
- SFDA Guidance for Borderline Products Classification
- The FDA Releases Compliance Policy for Registering Cosmetic Product Facilities and Listing Cosmetic Products.
- The Danish Medicines Agency - 2023 Deadline for Submitting Applications Concerning Marketing Authorisations and Clinical Trials
- MHRA Joins Global Regulatory Partners in Celebrating Ten Years of International Medicines Regulatory Cooperation
- Food labels by FSSAI will feature a QR code to assist individuals with visual impairments.
- ANVISA and ANMAT Sign Agreement on Easing Regulatory Requirements for Low-Risk Medical Devices
- ANVISA Updates Import Consent Request Procedure with Mandatory Pre-Boarding
- PMDA - Publication of Foreign Manufacturer Certification/Registration Number
- TGA Global Event Promotes Side Effect Reporting
- Formal authorization issued by the Food Safety and Standards Authority of India (FSSAI) approving the utilization of Rapid Analytical Food Testing (RAFT) kits, equipment, or methods for screening and surveillance objectives.
- India and Netherlands sign a Memorandum of Intent to Cooperate on Medical Product Regulation
- MDA Important Announcement Medical Device AD Application 2023
- MHRA - Early Access to Medicines Scheme Applications: Pending, Refused, Granted
- FDA Approves New Medication for Chronic Weight Management
- CTPA's media connections regarding the EU glitter prohibition, hair straighteners, and nasal spray tanners.
- Amendments to Turkish Food Codex on Baby Formulas and Follow-up Formulas (Communiqué No: 2019/14)
- The Danish Medicines Agency - First electronic product information published for medicines
- MHRA - Human and Veterinary Medicines: Register of Licensed Manufacturing Sites
- MHRA - Common Issues Identified During Clinical Trial Applications
Mergers & Acquisitions
- The Regulatory Maze: A Roadmap for Placing Your Medical Device on the EU, UK, and Switzerland Markets
- Exceptions and Modifications to Good Pharmacovigilance Practices
- Pharmacovigilance: Redefining Drug Safety with AI and Technological Innovations
- 11 Must-know FAQs about the Drug Approval Process in Japan
- The Human Element in Artwork Quality Checks: Skills and Expertise Required
- Finding the Right Fit: Strategies for Hiring Regulatory Artwork Management Talent
- Unlocking the Potential of South Korea's Pharmaceutical Industry: An Overview of the NDA/BLA Process
- MoCRA & GMP: Ensuring Quality and Safety in Cosmetic Manufacturing