Blog _Blog ICH and its influence on global regulation Read more » May 20, 2025 _Blog Paediatric Investigation Plans & paediatric requirements in the EU Read more » May 20, 2025 _Blog Understanding EUDAMED: The European Database on Medical Devices Read more » October 14, 2024 _Blog MDR Transition: New Responsibilities and Major Changes in the Medical Device Industry Read more » October 4, 2024 _Blog Biological medicinal products substitution in France? Read more » July 24, 2024 _Blog How to open a pharmaceutical establishment in France? Read more » July 2, 2024 _Blog The Jardé Law and Research Involving Human Subjects (RIPH): How Are Pharmaceutical Companies Affected? Read more » June 28, 2024 _Blog The Excellence of ATESSIA’s CMC: Your Partner in Technical and Regulatory Affairs Read more » June 13, 2024 _Blog The Post-Approval Change Management Protocol or “PACMP” Read more » June 13, 2024 _Blog What are Good Manufacturing Practices (GMP) ? Read more » May 29, 2024 _Blog What are CEPs ? Read more » April 29, 2024 _Blog What is the European Pharmacopeia ? Read more » April 29, 2024 Page1 Page2 Page3 Page4
_Blog MDR Transition: New Responsibilities and Major Changes in the Medical Device Industry Read more » October 4, 2024
_Blog The Jardé Law and Research Involving Human Subjects (RIPH): How Are Pharmaceutical Companies Affected? Read more » June 28, 2024
_Blog The Excellence of ATESSIA’s CMC: Your Partner in Technical and Regulatory Affairs Read more » June 13, 2024
