Chandrasekar Elangovan
19 February 2026
Overview of Regulatory Affairs for Medical Devices
10-hour
Medical Device Classifications, Conformity Assessment Routes, General Safety and Performance Requirements, Technical Documentation and other regulatory aspects of the QMS, Clinical Evaluation, Post Market Surveillance (PMS), PMCF & Vigilance, Risk Assessment and Management.
Anne Jury
Distributed by:
CE

Issued to

Chandrasekar Elangovan

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Credential Verification

Issue date: February 19, 2026

ID: cff45919-f922-485a-b78c-f8c9f63c99ca

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Issued by

Educo Life Sciences

Educo Life Sciences is a learning and development specialist that provides technical training solutions to the pharmaceutical, biotechnology, cell and gene, and medical device industries. ,

Type

Course

Level

Professional

Price

Paid

Description

The holder of this certificate attended an Educo Life Sciences training course as outlined on the certificate.

Earning Criteria

Participation

Attended the course held by Educo Life Sciences.

Watching

Or watched the recorded materials for the course held by Educo.