Webinar On FDA Inspection and Medical Device Design Control

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Category Medical Devices

Deadline: July 28, 2015 | Date: July 28, 2015

Venue/Country: Canada, Canada

Updated: 2015-06-26 17:43:14 (GMT+9)

Call For Papers - CFP

This 60-min presentation will provide great opportunities to get familiar with design control requirements and the FDA inspection concerning design control systems applicable to all types of medical devices including IVDs.

This webinar is a must for medical device and IVD firms including anyone interested in the topics from other industry.

Areas Covered in the Session :

Applicable Laws and Regulations

Definitions

Design Control Requirements

Design and Development Planning

Design Input and Design Output

Design Review

Design Verification And Validation

Design Transfer and Design Changes

Design History File (DHF), Device History Record (DHR) and Device Master Record (DMR)

FDA Inspection for Design Control

Common Mistakes and How to Avoid

How to Prepare for FDA inspection for Design Control

Best Practices for Establishing and Maintaining a Design Control System

Speaker’s Recommendation and Suggestions on PASS-IT Solutions

Who Will Benefit:

R&D

Quality

Regulatory Affairs

Compliance Officers

CEOs

VPs

Attorneys

Complainant Managers

Managers (RA, QA/QC, CA)

Consultants

Contractors and Subcontractors

Anyone interested in the topic

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

Customer Support : #416-915-4458

Email : supportcompliancetrainings.com