As part of our eLearning platform, the following courses will ba available very soon:


C001 - Clinical Research For Beginners (available) click here to enrol

C002 - Introduction to GCP (in preparation)

C003 - GCP updates, what is next to come (in preparation)

C004 - Monitoring Clinical Trials I (in preparation)

C005 - Monitoring Clinical Trials II (in preparation)

C006 - GCP Inspection, clinical trials audit (in preparation)

C007 - Clinical Trials Supplies (in preparation)

C008 - The Patient Information and Consent Process (in preparation)

C009 - GCP advanced comprehensive program (in preparation)

C010 - Clinical Research Data Management (in preparation)

C011 - Risk-based approach to monitoring (in preparation)

C012 - Drug Development Process (in preparation)

C013 - Pharmacology essentials for the Clinical Research Professional

C014 - Generic Drugs development and Bio-similars/ Subsequent entry biologicals (in preparation)

C015 - Safety Sureveillance and reporting in Clinical Research (in preparation)

C016 - Post marketing research and Registry studies (in preparation)

C017 - Code of Federal Regulations FDA- 21CFR312- Made it simple ( in preparation)

C018 - Code of Federal Regulations FDA - 21 CFR11 - Made it simple (in preparation)

C019 - Quality Assurance in Clinical Research (in preparation)

C020 - Standard Operational Procedures for the Sponsor of Clinical Trials

C021 - Introduction to Project Management in Clinical Trials (in preparation)


Courses required to obtain the Master certificate in Clinical Research (C001 to C016, C019 to C021), optional one of  the C017 or C018 plus and a Final Essay to be assigned.

The Diploma is issued by EduPharma and the Clinical Research Institute of America upon satisfactory completion of the courses, final exam and essay.

More information will follow.

For more info please contact us at info@grpc.ca