Scheduled On : Tuesday, October 22, 2013 at 10 AM PDT | 1 PM EDT
Duration : 120 Minutes
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Description :
In
Dec. 2010, the FDA has stepped up enforcement for 21 CFR 11 compliance
with spreadsheets being considered as low hanging fruit for FDA
inspectional findings.
Spreadsheet 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.
Spreadsheet 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 Session :
- Requirements for Excel Spreadsheets
- FDA Part 11 Validation Guidance
- Compliance Problems with Spreadsheets
- Design Specifications for 21 CFR 11 compliance
- Documentation for Part 11
- Future Trends in 21 CFR 11 compliance for Excel Spreadsheets
Who Will Benefit:
- Quality Managers
- Quality Engineers
- Small business owners
- GxP
- Consultants
- Quality VPs
- IT VPs
Speaker Profile
Angela Bazigos is the CEO of
Touchstone Technologies Silicon Valley, Inc. “Your Passport to
Compliance”. She has 30 years of experience in the Life sciences
industry spanning Project Management, Quality Assurance and Regulatory
Affairs and has a patent aimed at speeding up Software Compliance. Ms.
Bazigos is the president of PRCSQA (Pacific Regional Chapter of the
Society of Quality Assurance) a member of the SQA CVIC (Society of
Quality Assurance Computer Validation Initiative Committee), ASQ, DIA
and RAPS and consults to Pharma / Biotech / Medical Device companies as
well as investment groups on compliance matters, including strategy,
submissions, quality assurance and remediations following action by the
FDA. She teaches classes on Compliance, 21 CFR 11, Computer Systems
Validation, and Project Management both to investor groups and industry.
More recently, Ms. Bazigos co-authored Computerized Systems in
Clinical Research / Current Data Quality and Data Integrity Concepts
with FDA, DIA and Academia. She is on the board for UC Berkeley’s
Business School for Executive Education in Life Sciences and on the
Stanford Who’s Who Registry for contributions to the Life science
industry
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