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QMS&PMS

Part 7 Draft And Submit Periodic Risk Evaluate Report (PREP) To China NMPA

2021-10-01

This session of the webinar introduces the draft and submit periodic risk evaluate report (PRER) to China NMPA.…

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Part 6 Adverse Event Reporting Management Under Order 739

2021-10-01

This session of the webinar introduces the adverse event reporting management under order 739. The speaker list article…

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Part 5 How To Choose Distributors Who Are Compliant With NMPA Requirements In China?

2021-10-01

This session of the webinar introduces how to choose distributors who are compliant with NMPA requirements in China.…

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Part 4 Responsibilities And Potential Risks Of Medical Device License Holder In PMS.

2021-10-01

This session of the webinar introduces the the responsibilities and potential risks of medical device license holder in…

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Part 3 Medical Device Product Life Cycle Management With A Focus On Design Control

2021-10-01

This session of the webinar introduces the Medical device product life cycle management with a focus on design…

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Part 2 NMPA Medical Device QMS/GMP And Its Alignment With International Regulations Or Standards.

2021-10-01

This session of the webinar introduces the medical device QMS/GMP and its alignment with international regulations or standards.…

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Part 1 NMPA Medical Device Regulations/guidelines And Major Updates

2021-10-01

This session of the webinar introduces the medical device regulations/ guidelines and major updates. The speaker introduces the…

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