World Conference Calendar

32801 Conferences

The DHF, Technical File and Design Dossier - Similarities, Differences and The Future - Webinar by GlobalCompliancePanel

Added by davidross759 on 2010-08-12

Conference Dates:

Start Date Start Date: 2010-08-25
Last Date Last Day: 2010-08-25
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2010-08-24

Conference Contact Info:

Contact Person Contact Person: Support
Email Email: support@globalcompliancepanel.com
Address Address: Online Training Webinar, Wilmington, DE, 19801, United States
Phone Tel: 800-447-9407
Phone Fax: 302-288-6884

Conference Description:

This webinar will examine the existing and proposed requiements for the FDA's DHF and the MDD's TF/DD. Differing purposes / goals. Differing purposes / goals. Required and desirable contents. Areas requiring frequent re-evaluation / update. Similiarities and differences, and future trends. Typical DHF Table of Contents. Technical File or Design Dossier Table of 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. Differing approaches to file audits by the FDA and the Notified Body.

Areas Covered in the Session:

* The EU's MDD and the Technical File / Design Dossier
* Design Contol vs. a Product 'Snapshot in Time'
* DHF "Typical" Contents
* TF / DD Expected Contents
* Parallel Approaches to Documentation - Teams
* Future Directions
* FDA and NB Audit Focus
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