FDAnews Announces Spreadsheet Validation: Best Practices to Maintain Compliance Webinar Jan. 14, 2021

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Excel spreadsheets must receive FDA validation. Wouldn’t it be nice to know — in advance — what the agency looks for? Better read this now.



Spreadsheet Validation:
Best Practices to Maintain Compliance
An FDAnews/CenterWatch Webinar
Thursday, Jan. 14, 2021, 1:30 p.m. - 3:00 p.m. EST

Perch on the shoulder of an expert on spreadsheet validation...look on in real time as he highlights potential pitfalls and defines innovative validation approaches...ask why he does this instead of that...and get feedback.

Discover the tips and tricks that will help one streamline the spreadsheet validation process for quick-and-final FDA approval.

Attendees will:

  • Discuss FDA examples of noncompliance and regulatory concerns with respect to 21 CFR 210-211, 21 CFR Part 11 and 21 CFR Part 820
  • Determine spreadsheet validation gaps the FDA targets
  • Choose an approach for efficient and repeatable validation that fits into a traditional QA and validation processes
  • Generate spreadsheet specifications and qualification protocols
  • Test spreadsheets and macros
  • Plan, manage and resource an effective project

Close the compliance gap before one faces FDA warnings and liabilities.

Interested in registering multiple sites?
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
to learn about our special multisite discount.

Webinar Details:
Develop World-Class SOPs that Minimize Human Error
An FDAnews Webinar
Wednesday, Jan. 13, 2021, 1:00-2:30 p.m. EST

$287 per site

Easy Ways to Register:
Online: https://www.fdanews.com/sophumanerror
By phone: 888.838.5578 or 703.538.7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations

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Michelle Butler
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