Effect of the new Annex 13 on Complaints and Recalls - ECA Academy
Implementation of Annex 13 of the EU GMP Guide
Guidance Document - Annex 13 to the Current Edition of the Good Manufacturing Practices Guidelines - Orion GMP Solutions
SARQA/DKG Conference 3-4 October SARQA/DKG Conference 3-4 OCTOBER 2002 Annex 13 Update An Industry Perspective Michael J Cooke Director, Global. - ppt download
GMP for IMPs in View of the Revision of the EU Clinical Trial Provisions
Implementation of Annex 13 of the EU GMP Guide
Selection of European legal documents relevant to radiopharmaceuticals | Download Table
Clinical Trial Requirements U.S. vs. EU Similarities and Differences
ATMPs, Medicine Shortages & CTR: April 2022… | NSF International
Annex 13 - Manufacture of Investigational Medicinal Products
PIC/S revises GMP guide to reflect new EU clinical trials regulation | RAPS
GMP UPDATE - WHAT IS NEW IN THE EU - PART I - GMP Journal
Pharmaceuticals | Free Full-Text | Quality Assessment of Investigational Medicinal Products in COVID-19 Clinical Trials: One Year of Activity at the Clinical Trials Office | HTML