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    Conference about Key Factors to Write an Effective Standard Operating Procedure

    View: 218

    Website http://bit.ly/Standard_Operating_Procedure | Want to Edit it Edit Freely

    Category what are key factors for effective SOP, Work Instructions in SOP, Standard Operating factors

    Deadline: May 11, 2016 | Date: May 12, 2016

    Venue/Country: Online Event, U.S.A

    Updated: 2016-04-12 19:00:01 (GMT+9)

    Call For Papers - CFP

    Overview:

    This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.

    It will begin with a strategic view of SOPs in a company and how SOPs can help streamline operations in addition to ensuring regulatory compliance. This will be followed by explanation on how to get from regulations to the SOP. Finally, Best Practices for creating, implementing and maintaining SOPs using a risk based approach and getting SOPs ready for inspection will be presented.

    Why you should attend:

    Standard Operating Procedures (SOPs) are required by law for companies that are regulated by the Code of Federal Regulations such as Title 21 and Title 493. Yet there is no guidance on how to write, organize and maintain SOPs. Consequently, SOPs are frequently written in a way that makes compliance difficult or downright impossible. Worse, this often leads to many regulatory errors that first come to light during an FDA audit.

    This webinar will show you how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.

    Areas Covered In the Session:

    SOPs and their relation to the regulations

    SOPs as part of the company's regulatory infrastructure

    SOP on SOPs and how to ensure conciseness, consistency and ease of use

    Risk Based approach on SOP Best Practices for creation and maintenance

    Training on SOPs

    Tools for SOP tracking and when is validation required

    What the FDA looks for in SOPs during an inspection

    Who will benefit:

    Anyone that creates / maintains SOPs

    VP, Director, Manager of any dept that writes SOPs or performs training

    QA / QC

    Regulatory Affairs

    Speaker Profile:

    Angela Bazigos , is the Chief Compliance Officer of Morf Media. She has 40 years of experience in the Lifesciences industry spanning GLP, GCP, GMP, Medical Devices & 21 CFR 11 and has a patent aimed at speeding up Software Compliance.

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com

    http://www.compliance4all.com/

    Event Link : http://bit.ly/Standard_Operating_Procedure

    LinkedIn Like us – https://www.linkedin.com/company/compliance4all

    Twitter Follow us – https://twitter.com/compliance4all

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    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.