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    Online Training Special Considerations during Medical Device Design: Dos and Don'ts

    View: 235

    Website https://compliance2go.com/product/?pid=CP2014-392 | Want to Edit it Edit Freely

    Category Biotechnology , Medical Device

    Deadline: November 26, 2014 | Date: November 26, 2014

    Venue/Country: Houston, U.S.A

    Updated: 2014-11-10 15:52:59 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    This webinar is intended to discuss important aspects of medical device design and development.

    Under the Federal Food, Drug, and Cosmetic Act (FD&C Act or the Act), a medical device firm is subject to design control requirements, to the extent applicable during development including clinical trials and postmarketing.

    Based on the FDA enforcement trends, design control failure are frequently cited in 483s and FDA warning letters.

    FDA warning letters state “Failure to establish and maintain adequate procedures to control the design of the device in order to ensure specified design requirements are met.”

    In addition, due to device design control failures, it has resulted in many device recalls.

    This webinar is intended to provide guidance on what key considerations should be focused during medical device development under the surrounding circumstances. It is also intended to provide further guidance on how to establish and maintain design control procedures in a way to survive an FDA inspection applicable for all classes of medical devices including IVDs.

    In particular, this webinar will discuss various device design failures as examples to greatly In particular, this webinar will discuss various device design failures as examples to greatly increase our awareness.

    It should be noted that an adequate understanding, interpretation, and implementation of design control system requirements in a holistic manner can significantly contribute to your product quality and regulatory compliance, helping to ensure your innovative medical products safe and effective on a global market. As a result, your adequate implementation of design control will significantly contribute to saving an enormous amount of your unnecessary time, efforts and investment for a long term.

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

    This webinar will provide great opportunities to streamline device design and development process including regulatory approval/clearances and postmarketing.

    Why Should you Attend

    You need to ask sets of questions during medical device concept phase for developing intended use/user needs.

    It is important to ensure you are familiar with the regulatory requirements applicable for medical device design and development.

    Based on the regulatory requirements, firms shall establish and maintain adequate medical device design control procedures.

    Areas Covered in the Webinar

    Statutes and Regulations

    Device Design Concept

    Definitions

    Design and Development Planning

    Key Considerations

    Design Control System Components

    Design Control Sub-Systems

    Design Input and Design Output

    Design Review

    Design V and/or V

    Design Transfer and Design Changes

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

    Common Mistakes and How to Avoid

    How to Prepare for FDA inspection for Design Control

    Best Practices based on Actual Cases

    Speaker’s Recommendation and Suggestions on PASS-IT Solutions

    Who will Benefit:

    Regulatory affairs (associates, specialists, managers, directors or VPs)

    Quality professionals (associates, specialists, managers, directors or VPs)

    R&D (engineers, scientists, managers, directors or VPs)

    Complaint and risk management personnel

    Consultants

    Contractors/subcontractors

    CEOs

    VPs

    Clinical affairs (associates, specialists, managers, directors or VPs)

    Other interested parties

    Webinar Includes:

    Q/A Session with the Expert to ask your question

    PDF print only copy of PowerPoint slides

    60 Minutes Live Presentation

    Certificate of Attendance


    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.