The Clinical Research, Drug Safety and Pharmacovigilance Diploma program is designed to develop specialized knowledge and skills required to design and write study protocols, monitor and manage clinical trials and to conduct drug safety and Pharmacovigilance activities including adverse reaction reporting, preparing periodic safety update reports and in, establishing and managing Risk Evaluation and Mitigation Strategies in compliance with Canadian, US regulations and international guidelines. The program focuses on the global as well as Canadian health care system and regulatory agencies, health care legislations, international guidelines, and standard operating procedures (SOP) and practices for managing clinical studies and drug safety activities. Using practical and current real cases, AAPS integrated a unique approach and provides students with the foundation and practical knowledge to formulate a sound clinical development plan; ensure clinical trial data is credible and accurate; and that the rights, integrity and confidentiality of trial subjects are protected.
AAPS graduates from the Clinical Research, Drug Safety and Pharmacovigilance program pursue careers in the Pharmaceutical, Biotechnological, Medical devices, Cosmetics, Natural health Products, and Allied industries. |
These courses are intended as guidelines. Speak to your guidance counsellor to see what courses are offered at your school.
Please contact the school for information. |
* We make every attempt to provide accurate information on prerequisites, programs, and tuition. However, this information is subject to change without notice and we highly recommend that you contact the school to confirm important information before applying.
