THIS COURSE WILL DESCRIBE THE REGULATORY AND BUSIN 2013 - Live Webinar on Excel Spreadsheet Compliance with 21 CFR 11 By Angela Bazigos
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Category Medical Device
Deadline: March 19, 2013 | Date: March 20, 2013
Venue/Country: Houston, U.S.A
Updated: 2013-02-15 16:49:55 (GMT+9)
Call For Papers - CFP
This course will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application.Why should you AttendSpreadsheet Applications such as MS Excel are frequently used in 21 CFR 11 compliant environments, but they were not specifically designed for regulated environments and their development is not optimized for 21 CFR 11 compliance. However, the FDA expects that spreadsheets be compliant and lack of compliance can result in a warning letter. Consequently, validation of Excel Spreadsheet Applications is required as part of a 21 CFR 11 compliant environment. Areas Covered in the Session1. Requirements for Excel Spreadsheets2. FDA Part 11 Validation Guidance3. Compliance Problems with Spreadsheets4. Design Specifications for 21 CFR 11 compliance5. How does the FDA Design and Use spreadsheets6. Documentation for Part 117. Future Trends in 21 CFR 11 compliance for Excel SpreadsheetsWebinar Includes:Q/A Session with the Expert to ask your questionPDF print only copy of PowerPoint slides90 Minutes Live PresentationWho will BenefitQuality ManagersQuality EngineersSmall business ownersInternal and external auditorsManagement RepsFDA inspectorsConsultantsAbout SpeakerAngela Bazigos is the CEO of Touchstone Technologies Silicon Valley and has almost 30 years experience in Life Science. She applied for a patent to speed up computer systems validation and FDA software audits in the life sciences industry which was approved in June 2012. She has co-authored “Computerized Systems in Clinical Research” with the FDA, DIA and Academia and teaches classes in Project Management, 21 CFR 11, Computer Systems Validation (CSV), Quality Assurance and IT. She is the Vice President of the Pacific Regional Chapter of Society of Quality Assurance and writes articles for the SQA journal. She is also a member of DIA, RAPS and CVIC. She was recently inducted into Stanford’s Who’s Who for contributions to the Life Sciences industry.Ms. Bazigos has worked in various capacities at Roche, Price Waterhouse Coopers, Incyte Genomics, Abgenix, Novartis, Chiron, Applied Biosystems, Clinimetrics, and Veracyte, respectively. More recently, Ms. Bazigos was recognized as an industry subject-matter expert by the FDA and DIA. Ms. Bazigos graduated from North Staffordshire University (England, UK) with an MSc in Computing and University of Reading (England, UK) with a BSc in Microbiology & Biochemistry.Speaker : Angela BazigosProduct ID : F62189Schedule Date :Wednesday, March 20, 2013duration : 01:00 to 02:30 PM EDThttps://compliance2go.com/index.php?option=com_training&speakerkey=13&productKey=28
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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