Webinar: Facilitate the Medical Device Design Controls with Modern Requirements


September 30, 2020 | 11 AM EST

Constant development and innovation in medical devices are critical in ensuring personal health and safety. Organizations that want to succeed must adhere to evolving regulatory compliance when it comes to medical devices, and Requirements Management is a crucial component towards documentation and success. In this webinar, we will explore how to manage medical device design controls more efficiently using Modern Requirements.

Key Learning Objectives:

  1. Overview of the typical Medical Device Design Controls process and associated key tasks
  2. Documenting and Reporting for the Design History File (DHF)
  3. Formal review and E-signature for 21 CFR part 11 FDA and ISO 13485:2016
  4. Applying Change Management and Traceability to modifications or improvements of every stage of the design processes
  5. Automatic hazardous risk scoring

Our Speakers:

Bob Savelson

SVP Sales & Marketing
Modern Requirements

Asif Sharif

Chief Technologist
Modern Requirements

Mao Mao
Customer Success Consultant
Modern Requirements

Only submissions with valid email and company names will be considered

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