Validation and Control of Excel Spreadsheets in Regulated Environments
- Speaker:Ludwig Huber
- Date: 29th November 2018 10:00 AM PST | 01:00 PM EST
- Product Code:GRC-90438
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Excel Applications are widely used in laboratories, offices and manufacturing e.g., for data capture, data manipulation and report generation. Regulations such as HIPAA, Sarbanes Oxley Act and FDA's GxP 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® requirements can be met. For example, the FDA is widely using Excel® and complies with its own regulations.
- Regulatory requirements for spreadsheets; FDA Part 11 and GxP
- Recent FDA inspectional observations and warning letters
- Recommendations from the new GAMP®5 and EU Annex 11
- How to design spreadsheets for compliance.
- How to design, ensure and validate spreadsheet integrity.
- When, what and how much to test?
- Validation of standard/native Excel functions?
- 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
For easy implementation, attendees will receive
- SOP: Validation of spreadsheet applications
- SOP: Development and use of spreadsheets in regulated environments
- Gap analysis/checklist for Macros and Spreadsheet applications
Who will benefit:
- Developers and users of spreadsheet templates
- Lab Supervisors and managers
- QA managers and personnel
- Teachers and more
- Manufacturers of Pharmaceutical drug substances (APIs)
- Contract laboratories
- Medical device companies
- Clinical testing
- CROs and others
Ludwig Huber, Ph.D., is the director of Lab compliance and editor of Lab Compliance. He 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 CFDA, , ISPE, Japan PDA, PIC/S and several other national health care agencies.