Top Industry News
- DANISH 2022 Deadline for Submitting Applications Concerning Marketing Authorisations and Clinical Trials
- FDA In Vitro Permeation Test Studies for Topical Drug Products Submitted in ANDAs
- SFDA Guidance for Submission
- ANVISA Nutrition Labeling: Check the Amendments to the Rules
- PMDA Adapts Guidance on Product Identification Codes to Regenerative Medicines
- MHRA Software and AI as a Medical Device Change Programme
- FDA Issues Final Guidance About Multiple Endpoints in Clinical Trials
- EMA Updates Guidance for Applicants Seeking Scientific Advice and Protocol assistance
- PMDA Information on Risks, etc. During Evaluation of Pharmaceuticals