Developing and Implementing an Effective SOP in Healthcare Industry - Webinar

  • ID: 4383919
  • Webinar
  • 60 Minutes
  • Global Compliance Seminar
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In healthcare business environments, it is critical to define, document and implement an effective standard operating procedure (SOP) to ensure relevant business practices are done in a consistent, reliable, and effective manner - each and every time. Implementing an effective SOP has been under-valued by business owners for various reasons (e.g., due to perception for no need).

Effective SOPs can significantly help healthcare business owners save an enormous amount of time, energy, financial resources and beyond.

This webinar is intended to help you develop and implement guidelines for developing and implementing an effective SOP using a CAC-SI method. CAC-SI in this case refers to a Current, Accurate, and Comprehensive (e.g., SOP) in a Systematic, Integrated Manner.

In this 60-min presentation, the speaker will guide you through the details of the contents for your integration in your practical and actionable SOP. At the end of the presentation, you should be able to come up with your practical, actionable, and sustainable solutions to your organizations.

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  1. SOPs: Definitions and Why?
  2. When are SOPs needed?
  3. Who should develop an SOP?
  4. Requirements in the SOPs
  5. Writing an effective SOP
  6. Contents and format of SOPs
  7. How to implement SOPs
  8. Training employees with the SOPs
  9. Practical, Actionable, and Sustainable Solutions (PASS)
  10. Speaker’s Experience and Actual Cases.
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  • David Lim Dr David Lim,
    President and Principal Consultant ,
    Regulatory Doctor


    Dr. David Lim, Ph.D., RAC, ASQ-CQA. Dr. Lim is President and Principal of Regulatory Doctor. Dr. Lim frequently presents global regulatory and quality compliance topics in various forums and meetings. Recently, Dr. Lim developed 510(k) templates ready for use compliant with e-Copy and RTA policy. In addition, Dr. Lim developed FDA inspection checklists for drug and medical device manufacturers based on his analysis of FDA inspectional observations cited in 483s for the past seven years. Dr. Lim provides his feedback to regulatory agency (e.g., US FDA) through public comments and also served as a panel member during the FDA’s transparency public meeting in 2009. Dr. Lim contributes to the Regulatory Affairs Professional Society (RAPS) as an author and speaker. Dr. Lim leads and directs all research projects including, but not limited to, pharmacovigilance, medical device reporting, recalls and patient safety signals being conducted at the Regulatory Doctor.

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  • Healthcare Business Owners
  • Recruiters
  • Consultants
  • Regulatory Affairs Professionals
  • Clinical Affairs
  • Quality
  • Marketing
  • Senior Management
  • Contractors and subcontractors
  • Consultants
  • Anyone interested in the topic.
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