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
Issued to
Chandrasekar Elangovan
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Credential Verification
Issue date: February 19, 2026
ID: cff45919-f922-485a-b78c-f8c9f63c99ca
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.