More CDER published Q&A Catalogue for Generic Drug Authorisations
More EMA: Update of the Q&A Documents "Centralised Procedures"
More Updated Version of the Q&As regarding the Clinical Trials Regulation
More New JP Draft 2.28 Circular Dichroism Spectroscopy Published for Public Comments
More Counterfeit Protection - Amendment of Delegated Regulation (EU) 2016/161
More MHRA Guidance for the Supply of Medical Cannabis Products
More Four JP Drafts Related to Chromatography Published for Public Comments
More New General Ph. Eur. Chapter 2.1.7 Balances for Analytical Purposes
More Record Number of Fake Drugs seized during INTERPOL Operation
More Revised IPEC GDP Audit Guide for Pharmaceutical Excipients
More Absence of Approved Storage Facilities leads to GDP Non-Compliance Report
More EDQM updates Guidance for Electronic Submission of CEP Applications
More New FDA Draft Guidance for Industry on Bioequivalence Studies
More Consultation on Amendments on Pharmacovigilance Activities