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    IQ, OQ, PQ - Verification and Validation for Medical Devices

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    Website https://www.complianceonline.com/iq-oq-pq-verification-validation-for-medical-device-webinar-trainin | Want to Edit it Edit Freely

    Category

    Deadline: December 06, 2019 | Date: December 06, 2019

    Venue/Country: U.S.A

    Updated: 2019-11-02 02:32:52 (GMT+9)

    Call For Papers - CFP

    Verification and validation are important elements of the Quality System Regulations and ISO13485. This course will cover validation essentials for medical device manufacturers. You’ll learn which processes needed to be validated and what steps are required to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and change management. We’ll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices. A validated process is optimized ensure predictable and improved quality and compliance results.

    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.