Top Industry News
- New Zealand MEDSAFE Updates Overview of New and Changed Medicine Regulation
- EMA Use of Clinical Trials Information System Becomes Mandatory for New Clinical Trial Applications in the EU
- SFDA Guideline on Good Pharmacovigilance Practices (GVP)
- FDA Considerations for the Design and Conduct of Externally Controlled Trials for Drug and Biological Products
- EMA Shares Guidance on CTR, Confidential Data as New Rules Take Effect
- FDA M13A Bioequivalence for Immediate-Release Solid Oral Dosage Forms
- MHRA Human Medicines: Register of Electronic Export Certificates