This postgraduate comprehensive education program provides training in the field of medical product development at an advanced level and is especially designed for professionals working within the pharmaceutical, biotechnology, and device industries, regulatory authorities, government and universities. ACDRS collaborates with a highly experienced international faculty with a network of experts in pharmaceutical medicine, medical product development, and regulatory sciences. Participation in the ACDRS provides an opportunity to integrate work and education, to discuss with experts face-to-face, to gain in-depth knowledge while building an international network, and to put this into perspective with your own career plan. Former course participants rate the program as a tremendous success and benefit to their work and career.
The syllabus of the ACDRS Course covers all aspects of global pharmaceutical medicine and medical product development sciences. This includes the discovery and development of new therapeutics, biopharmaceutical sciences, clinical pharmacology and trial methodology, good clinical practice and ethics, pharmacovigilance, and risk management, biostatistics, regulatory affairs, health economics, project and portfolio management, marketing, and new therapeutic approaches. Participants will be involved in lectures, panel discussions, team-oriented case studies, and interactive learning.
“Attending ACDRS was one of the most rewarding experiences of my educational journey. It has helped me tremendously in my career. I felt so strongly about the value of this program that I joined the ACDRS family as a guest lecturer. It's not just what you gain in the time you spend at the sessions or the exceptional content, it's also the connections you make and the lifelong value you derive from it.”
–Mike Dyszel, Senior Director, Global Portfolio & Program Management, Mallinckrodt Pharmaceuticals