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    MEDICAL DEVICES 2011 - Design Control Explained - Webinar By ComplianceOnline

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    Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701878?channel=ourglocal | Want to Edit it Edit Freely

    Category Medical Devices,conference,event,Webinar

    Deadline: March 08, 2011 | Date: March 08, 2011

    Venue/Country: Palo Alto, U.S.A

    Updated: 2011-02-02 18:19:58 (GMT+9)

    Call For Papers - CFP

    Why Should You Attend:

    FDA expectations for compliance with the Design Control requirements according to the CFR 820.30 have increased significantly in recent years. A well established design control process can not only make the devices compliant but also can eliminate the unnecessary wastes from the system.

    This course will cover the essential areas of the Design Control and the methods to effectively improve / implement them within the existing or new product development process. The training will also cover the proven methods for effectively driving the entire process.

    Learning Objectives:

    Understanding the CFR requirements.

    Getting ready for FDA inspection.

    Understand key areas of Design Control.

    Implementation of Design Control in existing product development process.

    Interfaces with risk management & usability engineering process.

    NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.