Kruti Trivedi
- Role
- Senior Regulatory Affairs Specialist Cmc at Hikma Pharmaceuticals
- Location
- Edison, NJ, US
- LinkedIn followers
- 500 followers
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About Kruti Trivedi
Reliable and passionate regulatory affairs professional with 9 years of experience…
Experience
Senior Regulatory Affairs Specialist Cmc
Oct 2020 — Present
Skills
- Validation
- Post Approvals
- Microsoft Office
- Emerging Trends and Issue in Medical Device Industry
- Microsoft Excel
- Pharmaceutical Industry
- Research
- Regulatory Affairs
- Sop
- U.s. Food and Drug Administration (Fda)
- Gmp
- Andas
- Regulatory Requirements
- Pharmaceutics
- Standard Operating Procedure (Sop)
- Medical Device Regulations
- Regulatory Submissions
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