Sign for Notice Everyday    Sign Up| Sign In| Link| English|
Home Post Event 2025Event 2026Event By Topic By Country Contact

Our Sponsors


    THIS WEBINAR WILL GREATLY HELP MEDICAL DEVICE INDU 2013 - Medical Device Design Control - Webinar By GlobalCompliancePanel

    View: 415

    Website http://bit.ly/YELPxy | Want to Edit it Edit Freely

    Category Medical Device, Pharma, Biotech, Clinical, Drug, Food Safety, Heath,FDA

    Deadline: May 08, 2013 | Date: May 08, 2013

    Venue/Country: California, U.S.A

    Updated: 2013-04-22 19:27:22 (GMT+9)

    Call For Papers - CFP

    Overview: Understanding, interpreting, and implementing design control requirements in a holistic manner can significantly expedite the regulatory processes, bringing innovative medical products to the global market faster and saving enormous amount of your unnecessary time, efforts and investment.

    In this presentation, you will get familiar with regulatory and quality requirements of design control concerning medical devices, active implantable medical devices and IVDs.

    This webinar will greatly help medical device industry and relevant professionals establish and maintain adequate design control procedures.

    Why Should You Attend: Device manufacturers are required to establish and maintain the FDA-compliant quality management systems, where appropriate and applicable, including design control. This webinar is intended to provide guidance on understanding, interpreting, and implementing design control requirements. This presentation is further intended to help you establish and maintain adequate design control procedures for all classes of medical devices including IVDs.

    Areas Covered in the Session:

    Federal Statutes and Regulations Governing Medical Devices in the US

    Introduction and Definitions

    Design and Development Planning

    Design Input

    Design Output

    Design Review

    Design Verification And Validation including Software Validation

    Design Transfer

    Design Changes

    Design History File (DHF)

    Device History Record (DHR) and Device Master Record (DMR)

    Who Will Benefit:

    R&D Scientists, Engineers, Managers, and Directors

    Regulatory Affairs

    Quality Professionals

    Product Development Professionals

    CROs

    Consultants

    Senior Management

    Contractors and Subcontractors

    Anyone interested in design control

    Dr. Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal “Science.” Since then, Dr. Lim has held various positions at Duke, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences, Inc., A Luminex Company.

    Price: $225.00

    GlobalCompliancePanel

    NetZealous LLC,

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/YELPxy

    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.