Live Webinar On What the FDA looks for in SOPs during an inspection By Compliance2go

Start Date : 2012-03-06
End Date : 2012-03-06
Time : 10:30 am - 12:00 pm

Phone : 1.877.782.4696

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Location : United States of America
Online

Industry : Medical,Pharma; Research,Development;

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Description

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 and 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 Titles

Organized by

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10777 Westheimer Suite 1100 Houston, Texas United States of America 77042

About Speaker

 

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

Published by Compliance2go

Contact the Organizer

http://www.compliance2go.com/index.php?option=com_user&view=register

Country: United States of America.Event Categories: Seminar,Training and Webinar.Industry: Medical,Pharma and Research,Development.

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