This course provides a basic understanding of QMS and how it helps manage a product’s or process’s quality. It will help you understand how documents are structured, processed and the responsibilities required for quality management. This course also allows you to understand the document lifecycle in the quality management system.
Upon the completion of this course, participants would be able to:
● Describe how government regulations and requirements are satisfied to launch the product globally.
● Understand how statistical data can be used to improve process efficiency with reduced quality issues.
Who Should Attend
Students (B. Pharma/ M. Pharma/ B.Sc./M.Sc./ MBBS/ BDS), Industry peers, Regulatory professionals in pharmaceutical and healthcare sectors, academic research centers.