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    Webinar On Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)

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    Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1393 | Want to Edit it Edit Freely

    Category Food, Drugs & Biologics

    Deadline: January 13, 2015 | Date: January 13, 2015-January 14, 2015

    Venue/Country: Mississauga, Canada

    Updated: 2014-11-28 18:04:53 (GMT+9)

    Call For Papers - CFP

    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.

    Virtually every FDA inspection includes a review of SOPs and adverse agency findings are often the result of SOP administration issues.

    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 a 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:

    Quality Managers

    Quality Engineers

    Small business owners

    GxP

    Regulatory Affairs professionals

    Consultants

    Quality VPs

    IT VPs

    Regulatory VP

    CEOs

    Price tags:

    Live

    Single Live : For One Participant

    $ 249

    Corporate Live : For Max. 10 Participants

    $ 899

    Recording

    Single REC : For One Participant - Unlimited Access for 6 Months

    $ 299

    For more information and enquiries contact us at

    Compliance Trainings

    5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

    Customer Support : #416-915-4458

    Email : supportatcompliancetrainings.com


    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.