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Live webcast on Understanding Design Controls for Medical Devices By Compliance2go

January 19, 2012 Medical news in Houston,Texas, United States of America

Prior to introduction of a new device, or even a modified design for an existing device, a systematic process must be followed. This process must ensure that all requirements are met. A firm's design




FOR IMMEDIATE RELEASE
Houston, Texas, United States of America (Free-Press-Release.com) January 19, 2012 -- Understanding Design Controls for Medical Devices
Description
Discount: Get 15 % Discount as a early bird registrations. Use Promo code CGO15

Wednesday, March 28, 2012

Prior to introduction of a new device, or even a modified design for an existing device, a systematic process must be followed. This process must ensure that all requirements are met. A firm's design control process must meet all regulatory requirements, but at the same time not be so unwieldy as the present a barrier to timely market introduction. This webinar will cover the basics of design controls, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution. Documentation requirements for each design stage will be included as well.

Areas Covered in the Session:

- History of design control
- Design planning
- Design input/output
- Design reviews
- Design documentation
- Design transfer
- In-process design control

Who will benefit:

This webinar will provide valuable assistance to all companies that perform design activities. The employees who will benefit include:
R&D personnel and management
Process and Quality Engineers
QA management
Consultants
Quality system auditors


About Speaker

Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy products. In this position, Jeff is responsible for supplier management, during which he oversees supplier management, CAPA, and document control. Prior to this, Jeff spent 13 years at Life-Tech as the Director of Regulatory Affairs, where he was responsible for regulatory compliance of all aspects of the quality system. Jeff received his regulatory affairs certification in 1996.

Purchase formats: Live: $189.00 One Dial In - Unlimited attendance $249 Recorded: $289.00, CD: $349.00

For any assistance contact us at support@compliance2go.com or call us at 877.782.4696

https://compliance2go.com/index.php?option=com_training&speakerkey=15&productKey=84


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Contact Information

  • Name: Compliance2go

    Company: compliance2go

    Telephone: 877.782.4696

    Email: ***@compliance2go.com


  • About the author

    Compliance2go as the name suggests that without having proper adherence to the ever changing compliance rules and regulations, of the government any company needs to halt. The undying need for operational transparency ensures that the professionals are we



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