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    Bulletproofing your cGXP Documentation from Audit Citations

    View: 208

    Website http://www.onlinecompliancepanel.com/ | Want to Edit it Edit Freely

    Category

    Deadline: January 30, 2013 | Date: January 30, 2013

    Venue/Country: san francisco, U.S.A

    Updated: 2012-12-20 22:09:26 (GMT+9)

    Call For Papers - CFP

    Description:

    Regulators consider documentation to be a critical entity. Consequently, they always audit documentation systems and it is rare to find audits where 483s for poor documentation have not been issued.

    By attending this webinar, you will become familiar with what attributes contribute to good document development, the complexities and challenges posed by hybrid documentation systems and steps you absolutely need to take to ensure that your documentation system is bullet proof.

    Developing documentation to meet regulatory approval involves activities that record information and data either electronically or on paper. These documents should be developed such that they promote the easy dissemination of the information/data instead of confusing the operations.

    Why Should you Attend:

    The ability to write clear and concise documents is an essential skill required of those working in the Life Sciences industry. This course is ideal for all people who are required to create, complete and/or review documents in the Life Sciences industry.

    Objectives of the Presentation:

    At the end of the webinar, participants will:

    Become aware of document types audited

    Have exposure to examples of Quality attributes of documents

    Understand the regulatory requirements for electronic documents

    Become aware of the requirements for maintaining paper documents

    Become familiar with SOP requirements that auditors look for

    Review some Good Documentation Practices related 483s and WL

    Who can Benefit:

    Project Managers

    IT Engineers

    Design Engineers

    Documentation System managers

    Consultants

    QA Who review and approve raw data

    Regulatory Affairs Submission Personnel

    Pricing

    Live Session for one participant

    Price: $243.00

    Corporate Live Session 4 to 10 participants in single location.

    Price:$986.00

    Recorded Session Access recorded sessions only for one participant unlimited viewing for 6 months.

    Price: $288.00


    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.