Pharmacovigilance Manager

Designation

Department

Job location :

Responsibilities

I To independently review following applications online through Sugam Portal to CDSCO:

1. Import license of reference product for BE studies
2. BE study NOC for export purpose
3. Manufacture of new drugs to be introduced for the first time in India or to undertake clinical trial
4. Manufacture of fixed dose combination
5. Protocol amendment of clinical trial
6. Clinical trial site addition/ deletion/ closure or change in principal investigator
7. NOC for Form 29 for clinical trial samples
8. Manufacture of new bulk drugs (API)
9. Marketing of an already approved drug with new indication
10. Marketing of an already approved drug as a new dosage form or new route of administration
11. Marketing of an already approved drug as modified release dosage form.
12. Marketing of an already approved drug with additional strength
13. Export of biological sample
14. NOC for Form 29 for development purpose
15. Permission to manufacture and export API.

II. To review updated pack inserts

III. To review therapeutic rationale

IV. To review patient information leaflet

V. To initiate PIF

VI. To handle regulatory queries from various departments

VII. To screen updation of Indian regulatory guidelines on weekly basis

VIII. To prepare SOPs for Medicoregulatory Section

Qualification

Experience