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Validation and Use of Excel® Spreadsheets in FDA Regulated Environments - Webinar

  • ID: 4899824
  • Webinar
  • February 2019
  • Region: Global
  • 120 Minutes
  • Compliance Online
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Why Should You Attend:

Excel® Applications are widely used in laboratories, offices and manufacturing e.g., for data capture, data manipulation and report generation. Regulations such as FDA's GxPs and 21 CFR Part 11 require users of software and computer systems to demonstrate and document data accuracy, integrity and confidentiality. Out-of-the box Excel® has not been designed for regulated environments. However, with a good knowledge of Excel® capabilities combined with good procedures and practices on how to validate and use Excel® the requirements can be met. This webinar will demonstrate how requirements will be met.

Hand -Outs:

For easy implementation, Attendees will receive:

User Manual with Excel functions that help to comply with FDA requirements
SOP: Validation of spreadsheet applications
SOP: Development and use of spreadsheets in regulated environments
Gap analysis/checklist for Macros and Spreadsheet applications
Examples for validation documents
Note: These complimentary hand-outs will be sent to customers on request. Please email customercare@complianceonline.com for these documents, stating your order number, and they will be emailed to you within 4 working days.

Areas Covered in the Webinar:

FDA and other agency’s requirements for spreadsheet validation - What do inspectors ask and what documents should be available.
How to design spreadsheets for Part 11/GxP/SOX/HIPAA compliance?
Validation during design, development, installation and on-going use.
When, what and how much to test?
Dealing with standard Excel functions: Recommendations from GAMP5.
How to ensure and validate spreadsheet integrity and security for GxP and Part 11?
How to apply risk based validation to spreadsheet applications?
Validation of 'ad hoc' spreadsheet applications.
How to document planning, specifications, installation, testing and changes?
Examples from manufacturing, laboratories and offices.
Note: Product cover images may vary from those shown
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Dr. Ludwig Huber, Ph.D., is the director of Labcompliance and editor of www.labcompliance.com, the global online resource for validation and compliance. Dr. Huber is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems". He has given multiple presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. This included seminars, workshops and presentations for the US FDA, China SFDA, Korea MFDS, Singapore HSA, ISPE, Japan PDA, PIC/S and several other national health care agencies.
Note: Product cover images may vary from those shown