This course provides an introductory overview of the development of healthcare products and regulations across the globe. It will enable you with a basic understanding of the regulatory requirements essential to get marketing approvals for healthcare products. The course also includes an overview of different procedures for granting marketing authorization for medicinal products.
Upon the completion of this course, participants would be able to:
● Describe the origins of the regulatory system.
● Outline the regulatory processes associated with various healthcare products across the globe.
● Identify the regulatory systems and organizations in the UK, US, Europe, Canada, India, Australia, and Japan.
● Understand how medicinal products are regulated across the globe.
Who Should Attend
Students (B. Pharma/ M. Pharma/ B.Sc./M.Sc./ MBBS/ BDS), Industry peers, PAs, Administrators, and Support Staff associated with regulatory affairs and other related fields such as medical, manufacturing, marketing, and academic research centers.