Top Industry News
- FDA ANDAs: Pre-Submission Facility Correspondence Related to Prioritized Generic Drug Submissions
- FDA Statistical Approaches to Establishing Bioequivalence
- PMDA ICH Efficacy Guideline Update
- SWISS Public Consultation for ICH Guideline M11 “Clinical Electronic Structured Harmonized Protocol (CeSHarP)” Opened in Switzerland
- SWISS Meeting of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH)
- MHRA Clinical Trials for Medicines: Authorisation Assessment Performance
- Indonesia Technical Guidance for the Drug and Drug Laboratory at the POM Center in Palembang
- Singapore’s HSA finalizes LDT guidelines
- India to Update New Drugs and Clinical Trials Rules With Details of Non-Clinical Test Methods