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    Reduce Costs for Compliance with Data Integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

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    Website https://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-trai | Edit Freely

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    Deadline: February 16, 2020 | Date: February 26, 2020

    Venue/Country: Courtyard by Marriott Scottsdale Salt River, AZ, U.S.A

    Updated: 2019-12-30 16:39:59 (GMT+9)

    Call For Papers - CFP

    This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.

    It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation.

    The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.

    Understand the specific requirements associated with local and SaaS/cloud hosting solutions.

    It details the requirements for HIPAA Protect Health Information (PHI)

    Nearly every computerized system used in laboratory, clinical, manufacturing settings and in the quality process has to be validated. Participants learn how to decrease software implementation times and lower costs using a 10-step risk-based approach to computer system validation.

    The instructor reviews recent FDA inspection trends and discusses how to streamline document authoring, revision, review, and approval.

    Participants will learn how to write a Data Privacy Statement to comply with the EU General Data Protection Regulation (GDPR).


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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