Top Industry News
- FDA Submitting Documents Using Real-World Data and Real-World Evidence to FDA for Drug and Biological Products
- ANVISA New Rules for Nutrition Labeling Take Effect in 30 days
- SFDA Guidance for Priority Review of Product Registration
- PMDA Posts English-language Translation of Guide to Remote Inspection Procedure
- MHRA Medical Devices: Medical device stand-alone software including apps (including IVDMDs)
- FDA Leveraging Patient Preference Information in Medical Device Clinical Trial Design
- FDA General Clinical Pharmacology Considerations for Pediatric Studies of Drugs, Including Biological Products Guidance for Industry