Sign for Notice Everyday    Sign Up| Sign In| Link| English|

Our Sponsors

    Receive Latest News

    Feedburner
    Share Us


    Medical Devices for Risk Management Techniques 2017

    View: 322

    Website http://www.compliance4all.com/control/w_product/~product_id=501425LIVE?channel=ourglocal_Aug_2017_SE | Want to Edit it Edit Freely

    Category Risk Management Program, Medical Devices Webinars, FDA Expectations, Manufacturing Engineer trends, Regulatory Affairs, medical device industry, Stages of Risk Management, How to control those risks

    Deadline: August 21, 2017 | Date: August 22, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-06-15 15:16:35 (GMT+9)

    Call For Papers - CFP

    Overview:

    This course will help you understand the regulatory requirements, including

    ISO14971, and how to create processes and procedures to implement them.

    Why should you Attend:

    Many companies have even experienced class action law suits because of

    product quality issues. An effective program of risk management can help

    you proactively identify and mitigate product risks.

    Areas Covered in the Session:

    Overview of the ISO14971 standard as it applies to medical device

    companies

    Integrating the new standard with ISO 13485 as part of your overall QMS

    Conducting a review of the intended use of your device

    Stages of Risk Management as well as Tools and Techniques

    Judging the probability that harm may occur from those hazards

    Who Will Benefit:

    Design Engineer

    Manufacturing Engineer

    Quality Engineer

    R&D Personnel

    R&D Project Managers

    Quality Managers

    Auditors

    Regulatory Affairs Specialist

    R&D Manager

    Speaker Profile:

    Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the

    medical device industry with emphasis on quality, compliance, and six

    sigma. She has an extensive background in quality and compliance for

    medical devices from new product development, to operations, to post-

    market activities.

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com


    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.