2008 -
2008 Industrial Training and Internship @ MESHA PHARMA (P) LIMITED
Arnab Sarkar Education
Northeastern University
null
Arnab Sarkar Skills
Medical Device Regulation (MDR)
510(k)
CE marking
Regulatory Agencies
Clinical Strategy
Cross-functional Team Leadership
Professional Responsibility
Class III Medical Devices
Adobe Acrobat
Regulatory Affairs
FDA
Medical Devices
Pharmaceutical Industry
Regulatory Submissions
Regulatory Documentation
Regulatory Analysis
Device Registrations
Biotechnology
Technical Files
Regulatory Compliance
Regulatory Filings
Teamwork
Microsoft Excel
Quality Control
Quality Assurance
Regulatory Reporting
English
Microsoft Office
Customer Service
Research
Photoshop
Social Media
PowerPoint
Product Development
Public Speaking
Microsoft Word
Clinical Trials
SOP
Pharmaceutics
GMP
MDRs
UDI
Regulatory Dossier
Management
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Regulatory Requirements
Microsoft PowerPoint
Engineering
U.S. Food And Drug Administration Fda
Standard Operating Procedure Sop
Equity
Securities
u.s. Food and Drug Administration
Standard Operating Procedure
Arnab Sarkar Summary
Arnab Sarkar, based in United States, is currently a Principal Regulatory Affairs Specialist at Smith+Nephew. Arnab Sarkar brings experience from previous roles at Smith+Nephew, Bioventus and TIMI Study Group | Brigham and Women's Hospital | Harvard Medical Research. Arnab Sarkar holds a Northeastern University. With a robust skill set that includes Medical Device Regulation (MDR), 510(k), CE marking, Regulatory Agencies, Clinical Strategy and more. Arnab Sarkar has 3 emails and 1 mobile phone numbers on RocketReach.
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