Webinar: EU In Vitro Diagnostic Regulation (IVDR) Implementation. State of Play and Challenges
The webinar will be given by Todor Darakchiev, M. Pharm., Head of Division Medical Devices Department, Market Supervision and Inspections, […]
The webinar will be given by Todor Darakchiev, M. Pharm., Head of Division Medical Devices Department, Market Supervision and Inspections, […]
Regulation (EU) 2024/1689, commonly referred to as the “EU AI Act,” is considered the world’s first comprehensive regulation of artificial […]
Join us for an insightful webinar exploring the evolving professional identity within Pharmaceutical Medicine and medicines development. More information at […]
The 2024 revision of the Declaration of Helsinki included the Declaration of Taipei (DoT) for the secondary use of data […]
Practical challenges of implementing ICH-GCP(R3) in your clinical trials Please note that this webinar, a special virtual Workshop following the […]
Good Clinical Practice (GCP) is the international scientific and ethical standard for the conduct of interventional clinical trials. The ICH […]
The 2024 revision of the Declaration of Helsinki included for the first time the Declaration of Taipei (DoT) for secondary […]
The DoH is often recognized as the constitution of research ethics. Its latest revision encompasses all the fundamental principles that […]