The International Regulatory Affairs Network
MoT: Clinical Trial Management and Regulatory Affairs
13.04.2010 - 15.04.2010
Ort: Lausanne
Veranstalter: EPFL
Context: Managing and carrying out clinical trials, while respecting the legislative framework and good practices management. Dealing with regulations applying to medical devices and therapeutics.
Objectives: To develop understanding and competencies in the clinical trial process, in the regulations framework including the needed authorizations and approvals for medicines and devices.
