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    Spotlight on Complaint Handling and Medical Device Reporting

    View: 39

    Website https://www.complianceonline.com/complaint-handling-medical-device-reporting-webinar-training-706099 | Edit Freely

    Category

    Deadline: August 09, 2020 | Date: August 19, 2020

    Venue/Country: U.S.A

    Updated: 2020-07-06 19:52:01 (GMT+9)

    Call For Papers - CFP

    This webinar will help you to understand the expectations of complaint handling and medical device reporting. You’ll also learn about lessons from 483s and warning letters. We’ll discuss how you can develop your processes to efficiently and effectively manage complaints and MDRs. Also, we’ll discuss how to link these processes to failure investigation, recalls, and CAPA (Corrective and Preventive Action). We’ll cover best practices, so you can be prepared for an FDA inspection.

    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.