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Regulatory Training & Consulting

Expert 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

01. Drug Regulations & Overview of Health Canada

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)


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