Top Industry News
- ANVISA Updates the Regulatory Framework for Drug Labeling
- PDMA ICH M11 “Electronically Structured and Harmonized Clinical Trial Protocol (CeSHarP)” Guideline Draft Information Session
- FDA Content of Human Factors Information in Medical Device Marketing Submissions
- PMDA 4th ICH Forum: ICH Efficacy Guideline Update
- FDA Drug Products Labeled as Homeopathic Guidance for FDA Staff and Industry
- MHRA Human Medicines: Register of Electronic Export Certificates
- PMDA Explanations and Materials for Preparing Documents for Accreditation and Registration of Foreign Manufacturers of Pharmaceuticals, etc.
- MHRA Medicines: Apply for a Parallel Import Licence