Webinar Replay: Managing FDA Medical Device Compliance in Windchill

Webinar Replay: Managing FDA Medical Device Compliance in Windchill

In this webinar replay, explore how to Manage FDA Medical Device Compliance in Windchill!Windchill dashboards FDA Medical Device Compliance

  • Medical device manufacturers have an arduous process of managing all the relevant data (documents, BOM’s, drawings, ECN’s, etc.) of the DHF, DMR, DHR to ensure passing audits for FDA medical device compliance
  • See how Tristar is taking a new approach not only to report on this data, but actually dynamically collect, manage and give Dashboard status throughout the product development process

Space is limited! SIGN UP NOW to participate in the live product demonstrations and Q&A with our PTC Windchill expert.

Time listed: 11am US/Eastern

Bogdan Cudzilo FDA Medical Device ComplianceeMeet Your Presenter:

Bogdan Cudzilo serves as a Business Development Manager for TriStar. In his 10-year career, Mr. Cudzilo has developed domain expertise in the deployment and usage of Product Development Systems. He began his career in researching fracture damage resistance in aircraft composite structures, followed by contract work for a Tier 1 OEM aerospace supplier. Later he became involved in consulting and training in best practices for CAD and CAE for small and medium manufacturers in a variety of industries.

 


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