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Understanding Design

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					Live Webinar on : Understanding Design Controls for Medical Devices Wednesday, March
28, 2012 duration : 01:00 to 02:00 PM EST



                                        Description


                                        Prior to introduction of a new device, or even a
                                        modified design for an existing device, a systematic
Get 15 % Discount as an early bird
                                        process must be followed. This process must ensure
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                                        that all requirements are met. A firm's design control
 CGO15
                                        process must meet all regulatory requirements, but at
                                        the same time not be so unwieldy as the present a
Who will benefit                        barrier to timely market introduction. This webinar
                                        will cover the basics of design controls, and provide
                                        recommendations for implementation of a compliant
·      This webinar will provide        design control system. Also discussed will be design
                                        control requirements for devices already in
valuable assistance to all
                                        distribution. Documentation requirements for each
companies that perform design           design stage will be included as well.
activities. The employees who will
benefit include:

R&D personnel and management            Areas Covered in the Session

Process and Quality Engineers           - History of design control

QA management                           - Design planning


Consultants                             - Design input/output


Quality system auditors                 - Design reviews

                                        - Design documentation

                                        - Design transfer
                                      - In-process design control




purchase formats                      About Speaker:

    $189 One Dial In - One            Jeff Kasoff, RAC, is the Director of Quality at
Attendee                              Byrne Medical, a leading manufacturer of
                                      endoscopy products. In this position, Jeff is
     $249 One Dial In - Unlimited     responsible for supplier management, during
attendance (To be arranged in a       which he oversees supplier management, CAPA,
Conference room/Meeting room.         and document control. Prior to this, Jeff spent 13
Note : Only One Dial In Allowed)      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
    $289 On Demand (Recording         received his regulatory affairs certification in 1996.
available within 48 hrs after the
completion of the webinar)

    $349 Get Training CD



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                        Phone : 877.782.4696 | Fax : 281-971-0286
                          Email : Support@compliance2go.com

				
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