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    Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

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    Website https://www.complianceonline.com/complaint-handling-medical-device-reporting-and-recalls-seminar-tra | Edit Freely

    Category

    Deadline: January 27, 2020 | Date: February 06, 2020-February 07, 2020

    Venue/Country: Marriott Tampa Westshore, FL, U.S.A

    Updated: 2019-12-30 15:40:13 (GMT+9)

    Call For Papers - CFP

    Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.

    By attending this seminar, you will discover:

    How to overcome one of the biggest obstacles device manufacturers face

    How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling and documentation

    How and when to file Medical Device Reports (MDR), effective and appropriate communication with the appropriate regulatory agencies in the event of a recall.

    How to conduct a correction and removal actions to avoid a recall crisis, including required recordkeeping, expectation from FDA and other regulatory agencies in the event of a recall and key factors in implementing and maintaining compliance with the regulations and real life experiences of FDA.


    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.