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Health Canada Regulatory Training
SPharm provides training services to individuals and organizations to enable a practical understanding of the health product regulatory approval process. Our course materials are developed in-house and are constantly updated to keep current with industry practices and changing regulatory environments. The training we provide includes real-life examples with case studies and hands-on exercises to illustrate concepts and deepen your knowledge of the regulatory process to ensure that it is not only current, but also actionable.
Training Categories
02.New Drug Submissions (Standard, Priority, NOC/C, Fees, Appeals, etc)
03.Changes post NOC
04.The Common Technical Document
05.Clinical Trial Regulations
06.DIN Submissions
07.Pharmacovigilance (Regulations, Guidelines, Inspections)
08.Advertising
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