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Centre for Drug Regulatory Affairs has launched a???????????? ?????? ?? ??????? ???? ???????????. The course aims at providing a know-how of regulatory submission requirements for a generic drug to USFDA.

Objectives of the course:?

1. Understanding the stages of regulatory control.

2. Regulatory forms and procedures of USFDA.

3. Hands-on training in Pharma Ready? an eCTD software.

4. Detailed content and requirements of USFDA form.

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Duration:?15 hours

Timings:?09.30 am – 04.00 pm IST

Last Date for registration:?August 1, 2021

Coordinator:?Dr Krishnamurthy Bhat, Professor, Department of Pharmaceutical Quality Assurance, 沙巴体育 College of Pharmaceutical Sciences, 沙巴体育 Academy of Higher Education, 沙巴体育.

CLICK here to download the brochure