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

Angela Bazigos
Instructor: Angela Bazigos
Date: Tuesday April 13, 2021
Time:

10:00 AM PDT | 01:00 PM EDT

Duration: 3 Hours
Webinar Id: 20026

Price Details

Live Webinar
$290. One Attendee
$490. Unlimited Attendees
Recorded Webinar
$340. One Attendee
$540. Unlimited Attendees
Combo Offers   (Live + Recorded)
$549 $630   One Attendee
$799 $1030   Unlimited Attendees

Unlimited Attendees: Any number of participants

Recorded Version: Unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of live webinar)

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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