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    Good Documentation Practices to Support FDA Computer System Validation

    View: 239

    Website https://goo.gl/NCV7DV | Want to Edit it Edit Freely

    Category eu regulations food labelling, fda compliance, fda labeling requirements

    Deadline: November 03, 2017 | Date: November 03, 2017

    Venue/Country: CO, U.S.A

    Updated: 2017-10-05 13:41:43 (GMT+9)

    Call For Papers - CFP

    OVERVIEW

    This webinar will leave you with the information needed to create and maintain good documentation that meets FDA compliance standards. You will learn about what must be done and what must not be done. In addition, you’ll learn about the various computer system validation deliverables and how to document them.

    FDA requires that all documentation related to GxP products (GMP, GLC, and GCP) be created and maintained in accordance with specific rules. From the color of the ink used to the retention requirements, you’ll learn all about how to create and maintain good FDA-compliant documentation.

    WHY SHOULD YOU ATTEND

    You should attend this FDA regulatory compliance training if you are responsible for any FDA-regulated data and/or records. All documents need to be created and maintained in accordance with FDA guidelines for good documentation to avoid any issues during an inspection or audit. You will also benefit from learning about the guidelines for computer system validation and the many deliverable documents that need to be produced in a way that is FDA-compliant. Having completed this course, you will be on your way to successful future FDA audits and inspections.

    AREAS COVERED

    • FDA Good Documentation Practices

    • Computer System Validation (CSV)

    • System Development Life Cycle (SDLC) Methodology

    • GAMPV System Categorization

    • Industry Best Practices

    • Potential Pitfalls

    WHO WILL BENEFIT

    • Information Technology Analysts

    • QC/QA Managers

    • QC/QA Analysts

    • Clinical Data Managers

    • Clinical Data Scientists

    • Analytical Chemists

    • Compliance Managers

    • Laboratory Managers

    • Automation Analysts

    • Computer System Validation Specialists

    • GMP Training Specialists

    • Business Stakeholders responsible for computer system validation planning, execution, reporting, compliance, maintenance and audit

    • Consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance

    • Auditors engaged in the internal inspection of labeling records and practices

    All FDA-regulated industries:

    • Pharmaceutical

    • Biological

    • Medical Device

    • Tobacco

    LEARNING OBJECTIVES

    • To understand how to create, revise and maintain documentation that is FDA-regulated.

    • To understand the many deliverables required to complete a computer system validation effort.

    • To understand industry best practices.

    • To understand and avoid potential pitfalls.

    For more detail please click on this below link:

    https://goo.gl/NCV7DV

    Email: supportattrainingdoyens.com

    Toll Free: +1-888-300-8494

    Tel: +1-720-996-1616

    Fax: +1-888-909-1882


    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.