Introduction

Many citations by FDA and notified bodies include findings with respect to insufficient information in the Design History File, not following the procedures to make the device as established in the DMR, and incomplete or inaccurate production data of incoming,in-process and finished products. Is your company able to access all relevant documents detailing the design of your device? Is your DMR accurate and is it being followed? Can the operators access your DMR? Are you recording and documenting all your production and testing data and maintaining them in the DHR?


Areas Covered in the Session:


- DMR and outsourced design/production

- DMR and OEM relationships

- Controlling and maintaining DMR

- Device History Record (DHR)

- Definition

- Contents

- Using DHR data for tracking and trending

- DHR and outsourced design/production

- DHR and OEM relationships

- Technical File (TF)

- Definition

- Contents

- TF and outsourced design/production

- TF and OEM relationship

- Design/process changes and DHF, DMR, DHR, and TF



Who will benefit:



This Webinar is designed for people involved in document preparation and maintenance, and those who have involvement with documentation. This typically includes:



Quality Managers/Engineers

Production/Process Managers/Engineers

Manufacturing Managers/Engineers

QA and QC managers, inspectors, supervisors and personnel

Documentation Specialists
Supplier Quality Managers/Engineers

Venue

Compliance2go

Compliance2go, 10777 Westheimer Suite 1100 Houston, Texas United States of America, Houston, Texas, 77042, United States

Useful links

• Venue information More information about the venue

Organised by

Compliance2go

Contact information

Mr David Jones
10777 Westheimer Suite 1100 Houston, Texas United States of America 77042, Houston, Texas, 77042, United States of America
877.782.4696
Contact us by email

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