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.
02.New Drug Submissions (Standard, Priority, NOC/C, Fees, Appeals, etc)
03.Changes post NOC
04.The Common Technical Document
05.Clinical Trial Regulations
07.Pharmacovigilance (Regulations, Guidelines, Inspections)
Find out what SPharm can do for you.
Learn how our proven expertise can help reach your objectives faster. Contact us today.