Vishakha W.
- Role
- Sr Regulatory Consultant, Medtech at IQVIA
- Location
- Boston, MA, US
- LinkedIn followers
- 500 followers
Healthcare & Human ServicesView LinkedIn profile
About Vishakha W.
Detail-oriented, driven and self-motivated regulatory affairs professional with a strong…
Experience
Sr Regulatory Consultant, Medtech
Sep 2023 — Present
Skills
- Clinical Trials
- Quality Assurance
- Pmas
- Hplc
- Standard Operating Procedure (Sop)
- Research
- Microsoft Excel
- Biotechnology
- Microsoft Office
- High-Performance Liquid Chromatography (Hplc)
- Pharmaceutical Industry
- Microsoft Word
- Ind
- 510(K) Pre-Market Notification
- Regulatory Affairs
- 21 Cfr Part 11
- Good Clinical Practice (Gcp)
- Sop
- U.s. Title 21 Cfr Part 11 Regulation
- Cgmp Practices
- Gcp
- Gmp
- Internal Audit
- Nda
- Regulatory Submissions
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