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    Drafting a Software Verification and Validation Report Package and Protocol - The 11 Must-have Documents

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    Website https://www.complianceonline.com/drafting-a-software-v-and-v-documentation-package-and-protocol-21cf | Want to Edit it Edit Freely

    Category

    Deadline: December 04, 2018 | Date: December 04, 2018

    Venue/Country: U.S.A

    Updated: 2018-10-27 16:27:52 (GMT+9)

    Call For Papers - CFP

    A tougher U.S. FDA expects a company to maintain certain documents in equipment, process and product software V&V. These documentation requirements can assist in a 21 CFR Part 11 CGMP records / signature V&V as well. This training program will provide valuable assistance to all regulated companies in evaluating their existing or anticipated software V&V activities and documentation requirements, especially in light of the changes in the FDA's stance vis a vis industry compliance, past problems, and the growing cloud environment. It will help attendees understand and recognize the most common software V&V failings and their fixes. The webinar will allow attendees to develop and use a repeatable software V&V template for all software validation projects.

    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.