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    Secrets to Writing Effective SOPs for Medical Device QMS

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    Website http://c2gowebinars.com/product/?topic=sop-qms | Want to Edit it Edit Freely

    Category Medical Device

    Deadline: February 23, 2016 | Date: February 23, 2016

    Venue/Country: Online, U.S.A

    Updated: 2016-02-09 19:10:10 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    This webinar will help you ensure that your procedures that are complete, concise, and easy to follow. The FDA expects Medical Device manufacturers to “establish and maintain procedures”. You will learn what this means and how to comply with expectations.

    Why you should attend:

    Standard Operating Procedures (SOPs) are a basic ingredient of an effective quality management system. Yet, “inadequate SOP” observations still rank among the most frequently cited 483 and Warning Letter observations. SOPs are one of the first things an auditor/ investigator will review during and inspection. Well written SOPs send a message that your QMS is complete, accurate, and followed.

    This webinar will help you to write clear, unambiguous, and flexible SOPs. You will learn techniques for creating easy to read, clear, and concise SOPs that your employees can easily follow. Well written SOPs ensure that your employees understand and consistently follow processes.

    Areas covered in the Webinar:

    This 90-minute webinar will focus on how to write clear concise SOPs that your employees can follow. Topics to be covered include:

    FDA and NB expectations for SOPs

    Lessons Learned from 483s and warning letters

    Common problems with SOPs

    How to structure your QMS and SOPs

    How to outline and format your SOPs

    Using process maps to make procedures clear

    Using diagrams and visuals

    Maintaining and controlling SOPs

    Ensuring adequate training to your SOPs

    Best Practices

    Who will benefit:

    Quality Systems Specialists

    Document Control Specialists

    Quality and Compliance Specialists

    Internal Auditors and Managers

    Training Specialists

    CAPA Specialists

    Supplier Quality Engineers and Auditors

    Quality/Compliance managers or directors for Medical Device companies

    General Managers wanting to learn how to understand Quality System requirements

    Webinar includes:

    Q/A Session with the Expert to ask your question

    A copy of the PowerPoint slides

    90 Minutes Live Presentation

    Attendance of Certificate


    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.