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    Test Method Validation to Verify the Performance of a Medical Device

    View: 138

    Website https://www.compliance4all.com/control/w_product/~product_id=502393LIVE?channel=ourglocal_Apr_2019_S | Want to Edit it Edit Freely

    Category Test Method Validation, FDA Requirements, Validation Trainings, compliance trainings, test method validation and verification, analytical method validation test, validation procedure trainings, Online test courses

    Deadline: April 03, 2019 | Date: April 04, 2019

    Venue/Country: Online, U.S.A

    Updated: 2019-02-18 15:29:37 (GMT+9)

    Call For Papers - CFP

    Overview:

    Those who work with process optimization and validation focus on optimizing a process and reducing variability. Those working on Test Method Validation, on the other hand, focus on discerning between process variation and measurement error from the test method itself.

    Why should you Attend:

    This webinar will help you better understand Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.

    Areas Covered in the Session:

    When should Methods be Validated?

    Qualification vs Validation

    Types of Test Method Validations

    How to perform successful test method validations

    Who Will Benefit:

    Manufacturing Engineers

    Regulatory Affairs Teams

    Quality Assurance & Quality Control Teams

    Operations Teams

    Document Control

    Speaker Profile:

    Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, Jose served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

    Event Fee: One Dial-in One Attendee Price: US $150.00

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: compliance4all14atgmail.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.