Webinar On Key Regulatory Documents Design History File DHF Device Master Record DMR
This 90 minute webinar will examine the existing and proposed requirements for the U.S. FDA's DHF and the EU MDD's TF/DD. This webinar will provide valuable assistance to all regulated device companies that need to ensure their DHFs, TFs/DDs and associated and derivative documentation meet their respective requirements. It also addresses current requirements as well as some changes on the horizon.
Areas Covered in the Session :
How to meet and document their differing requirements.
Required and desirable contents.
Areas requiring frequent re-evaluation / update.
Similarities and differences, and future convergences and trends.
Typical DHF contents.
Typical Technical File or Design Dossier contents.
The importance and usefulness of the "Essential Requirements".
Structure of the "Declaration of Conformity"; self-declaring or N-B reviewed.
Parallel approaches to development.
Where the Device Master Record / Device History Record "tie in".
Differing approaches to records audits by the U.S. FDA and an EU Notified Body.
Who Will Benefit:
This webinar will provide valuable assistance to all regulated device companies that need to ensure their DHFs, TFs/DDs and associated and derivative documentation meet their respective requirements. Its principles apply to personnel / companies in the Medical Devices, Diagnostic, and to a lesser extent the Pharmaceutical and Biologics fields. The employees who will benefit include:
QA / RA
All personnel especially involved in device development, regulatory compliance and documentation.
Single Live : For One Participant
Corporate Live : For Max. 10 Participants
Single REC : For One Participant - Unlimited Access for 6 Months
For more information contact
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Learn More: Webinar On Key Regulatory Documents Design History File DHF Device Master Record DMR