Job Description
- Responsible to guide in preparation / update of Quality Management System Documents Responsible to prepare / review / update Design Master File, Technical Master File Responsible to prepare / review / update Technical documentation for the international registration of products.
- Responsible to prepare / review / update to get clinical trial approval from Drug Controller General India.
- Responsible to guide in preparation / update of Quality Management System Documents Responsible to prepare / review / update Design Master File, Technical Master File Responsible to prepare / review / update Technical documentation for the international registration of products.
- Responsible to prepare / review / update to get clinical trial approval from Drug Controller General India.