Live Webinar
on
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)
Date & Time: Tuesday, February 07, 2012
10:00 AM PST | 01:00 PM EST
Duration: 90 Minutes
Instructor: Angela Bazigos
Location: Online
Price : $245.00
Register Now
(for one participant)
Instructor Profile:
Overview:
Angela Bazigos CEO, Touchstone Technologies Silicon Valley
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 should you 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
Angela Bazigos is the CEO of Touchstone Technologies Silicon Valley, Inc. an FDA Compliance company. She has almost 30 years experience in the Lifesciences industry and has applied for patents aimed at speeding up Software Compliance. She is a member of the SQA CVIC (Society of Quality Assurance Computer Validation Initiative Committee), DIA and RAPS and teaches classes on 21 CFR 11, Computer Systems Validation, Compliance Strategy and Project Management. More recently, Ms. Bazigos was selected to co-author Computerized Systems In Clinical Research / Current Data Quality and Data Integrity Concepts with FDA, DIA and Academia. ...more
SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow. Suggest a Topic
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Click here to register for this webinar Who Will Benefit: l
Anyone that creates / maintains SOPs
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VP, Director, Manager of any dept that writes SOPs or performs training QA / QC
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Regulatory Affairs
It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely benefit from this program. For more information, please contact the event coordinator. We look forward to seeing you at the webinar. Best regards, Event-coordinator GlobalCompliancePanel
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