About Course

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.



Eligibilities



--- Health care and Pharmaceutical ---

(CMCCP) Chemistry, Manufacturing & Controls (CMC) Certified Professionalâ„¢

Total Days
28 Days

Total Hours
180 Hours

Batch Size
25 Members

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