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Angela Bazigos 2012 - How does the FDA Design and Use spreadsheets

Date2012-04-03

Deadline2012-04-03

VenueHouston, USA - United States USA - United States

KeywordsMedical Device

Websitehttps://www.compliance2go.com

Topics/Call fo Papers

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 Attend

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

1. Requirements for Excel Spreadsheets

2. FDA Part 11 Validation Guidance

3. Compliance Problems with Spreadsheets

4. Design Specifications for 21 CFR 11 compliance

5. How does the FDA Design and Use spreadsheets

6. Documentation for Part 11

7. Future Trends in 21 CFR 11 compliance for Excel Spreadsheets

Who will Benefit

Quality Managers

Quality Engineers

Small business owners

Internal and external auditors

Management Reps

FDA inspectors

Consultants

https://compliance2go.com/index.php?option=com_tra...

Last modified: 2012-02-14 21:03:16