Post Market Surveillance of Medical Devices: Foundation and Regulatory Context
In the fast-evolving landscape of medical devices, Post-Market Surveillance (PMS) is no longer a compliance formality—it's a strategic cornerstone for product success, patient safety, and regulatory longevity. This foundational course explores the global PMS ecosystem and equips you with a holistic understanding of how PMS interlinks with risk management, clinical evidence, vigilance, design control, CAPA, and management responsibility.
This is your pathway to mastering PMS as a proactive, data-driven lifecycle process!
Stay in touch, participate in Q&A and connect with other learners via our community 'PMS Learners', click here to join the community.
We also have weekly live sessions to clear your doubts. Please send your questions in advance to contact@neujinsolutions.com.
Note: The certificate will be shared over email upon successful completion of the course.
6 Lessons
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Module 1: Introduction to the Post Market Surveillance
Get Introduced to Post Market Surveillance. This module contains quiz and exercise.
Module 2: Designing a PMS system
Learn how to design a compliant and effective PMS System. This module contains quiz and exercise.
Module 3: PMS Data Evaluation & Continuous Improvement
Learn how to evaluate PMS Data and drive Continuous Improvement. This module contains quiz and exercise.
Module 4: Vigilance, Reporting and Field Actions
Learn about Vigilance, Regulatory Reporting and Field Actions. This module contains quiz.
Module 5: Building a Global PMS Culture
Learn how to build an organization wide culture that fosters PMS. This module contains quiz.
Module 6: Learner's Handout, Templates and Feedback
Summary of course and key take-aways