Profile Details

Create Project

★★★★★

☆☆☆☆☆

USD 120 /hr

★★★★★

☆☆☆☆☆

Hire Sweta S.

Singapore

USD 120 /hr

Experience in Handling Clinical and Regulatory Documents for CE approvals and regular certification Audit.

Profile Summary

Experience in Handling Clinical Evaluation Process for high risk medical device comprising of 1. Conduct of clinical Trial for the medical device. 2. Writing of Clinical trial report and presenting it in CER. 3. Writing of literature search plan and report and conducting the same. 4. Writing of PMCF plan and report and conducting the same 5. Writing of PMS plan and report and conducting the same.

Subject Matter Expertise

• ★ Clinical Evaluation Reports (CER)
• ☆ Product Development

Services

• Writing

Writing Technical Writing

Work Experience

Clinical affairs manager

Merlin MD Pte Ltd

February 2016 - Present

Education

Masters

Institute of Clinical Research

June 2007 - June 2009

Certifications

• Certification details not provided.