The course covers the requirements for regulatory submissions, good manufacturing practices,
and quality assurance throughout the product life-cycle. The course also includes topics such
as analytical chemistry, biostatistics, process validation, stability testing, and document management.
The course is suitable for individuals involved in the development and manufacture of pharmaceuticals,
biologics, and medical devices. The course is designed to equip the participants with the tools
and knowledge needed to manage their agency effectively and comply with the regulatory standards.
Foundar
Director
HR

IT Maneger