This course provides a detailed overview of the evaluation of Medicines Regulations in Europe. It also explains why the selling of medicinal products is restricted only to authorized personnel and how pharmaceutical industries are controlled and regulated. This course provides you with a basic understanding of the basic regulatory requirements to obtain marketing approval for healthcare products. It also helps you understand the concepts of patient safety and the efficacy of medicines.
Upon the completion of this course, participants would be able to:
● Describe the evaluation of medicines regulations.
● Outline the regulatory processes associated with various healthcare products in Europe.
● Importance of safety, efficacy, and quality in medical products.
Who Should Attend
Students (B. Pharma/ M. Pharma/ B.Sc./M.Sc./ MBBS/ BDS), Industry peers, Life sciences graduates.