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Post Market Surveillance

Post_market_surveillance

During the last years the request and requirements on PMS has increased and more is in the ISO 13485:2016 and the new Medical Device Regulation. This course will give an introduction to the regulations and guidance on PMS (plan and report) as well as the process interfaces.

About Post Market Surveillance

Goal:

To give an understanding of the PMS process, which is a life cycle approach for your medical device(s).

Who benefits:

Management, clinical affairs, design & development engineers, QA/RA specialists, risk managers, customer support/service and marketing.

Course Leader:

Anette Sjögren, PREVENTIA AB

Anette is a member of the Swedish (TK355 – ISO 13485, ISO 14971 and IEC 62366) and the international technical (TC210) committee and was also part of the international PMS task force.

Language:

Course material is in English.

Presentation in English or Swedish (depending on the participants).

Kontakt os for yderligere information

Do you have any questions?

Contact us

Register for the training class here

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Hvornår:

Add to calendar 2023/06/14 09:00 2023/06/14 18:00 Post Market Surveillance During the last years the request and requirements on PMS has increased and more is in the ISO 13485:2016 and the new Medical Device Regulation. This course will give an introduction to the regulations and guidance on PMS (plan and report) as well as the process interfaces.
https://www.dnv.dk/training/post-market-surveillance-156037
This only adds the event to your calendar, please remember to register for this event. false YYYY/MM/DD akeGphYOczrmtQTfhmEQ22349

Varighed:

1 day.

Pris:

Course fee: DKK 6.800,- (ex. VAT). Course material and certificate of participation is included in the price.

Yderligere information:

You can find our cancellation policy, terms & conditions and practical information about the course here: www.dnv.dk/betingelser

About Post Market Surveillance

Goal:

To give an understanding of the PMS process, which is a life cycle approach for your medical device(s).

Who benefits:

Management, clinical affairs, design & development engineers, QA/RA specialists, risk managers, customer support/service and marketing.

Course Leader:

Anette Sjögren, PREVENTIA AB

Anette is a member of the Swedish (TK355 – ISO 13485, ISO 14971 and IEC 62366) and the international technical (TC210) committee and was also part of the international PMS task force.

Language:

Course material is in English.

Presentation in English or Swedish (depending on the participants).

Interne kurser for din virksomhed

Kontakt os