3-Hour Virtual Seminar on Excel Spreadsheet Validation for FDA 21 CFR Part 11

In this Interactive session, the speaker will explain validation of Excel Spreadsheet Applications, which is required as part of a 21 CFR 11 compliant environment, as well as requirements for Excel Spreadsheets.

Angela Bazigos
Instructor:
Angela Bazigos
Date:
Friday, November 15, 2019
Time:
09:00 AM PST | 12:00 PM EST
Duration:
3 Hours

More Trainings by this Expert   Product Id : 502771

Price Details
$290 Live
$490 Corporate Live
$340 Recorded
$540 Corporate Recorded
Combo Offers
Live + Recorded
$549 $630 Live + Recorded
Corporate (Live + Recorded)
$799 $1030 Corporate
(Live + Recorded)
Price Detail Options
Overview:

Part 11 / Annex 11 Computer Systems Validation (CSV) is to be implemented in order to increase the integrity, accountability and security of the spreadsheets and achieve GxP Compliance.

CSV enables the level and rigor of specification and verification applied to spreadsheets to be based on spreadsheet risk, complexity, and novelty. This bootcamp will provide the attendees with the tools for successful computer systems validation for Excel Spreadsheets.

Areas Covered in the Session:

  • Types and Uses of Excel Spreadsheets (e.g. disposable spreadsheets, spreadsheets used as documents, etc.)
  • Computer Systems Validation for Excel (will cover 21 CFR 11, Annex 11)
  • Examples of Typical Approaches for Excel Validation
  • How to tailor your risk based methodology to Excel to determine the level of validation required

Who Will Benefit:
  • VP of IT
  • Director of IT
  • Quality Managers
  • Project Managers (for CSV / IT)
  • Validation Specialists
  • Database Administrators
  • System Administrators
  • Directors /Senior Directors of Discovery
  • Directors /Senior Directors of Development
  • Directors /Senior Directors of Commercialization
  • Document Managers
  • Training Managers
  • Regulators


Speaker Profile
Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services.

Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Microbiology, Food Safety & Turnarounds. Past employers / clients include Royal Berkshire Hospital, Roche, Novartis, Genentech, PriceWaterhouseCoopers & Stanford Hospital. Positions include Chief Compliance Officer,Director of QA and MIS Director. Co-authored & prototyped 21 CFR 11 guidance with FDA. Co-authored Computerized Systems in Clinical Research w/ FDA & DIA Patent on speeding up software compliance https://www.google.com/patents/US8266578.

Recently quoted in Wall Street Journal for using training to bring regulatory compliance to the Boardroom includes training for Society of Quality Assurance.

Comments / collaborates with FDA on new guidance documents. Former President of Pacific Regional Chapter of Society of Quality Assurance. Stanford's Who's Who for LifeSciences.




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