Validation of Excel Spreadsheet for Use in FDA Regulated Environment
Date: May 12, 2025
Duration: 60 Minutes
Time: 12 PM EST
Why should you attend:
Capability to use Excel creates an inexpensive and handy tool for FDA regulated industry, particularly R&D operations and early-stage development activities. However, companies frequently struggle with understanding and implementing applicable regulations on spreadsheets. Many companies use invalidated spreadsheets leading to negative audit findings. This seminar will address all these issues by providing methods for planning and executing excel spreadsheet validations that satisfy FDA requirements.
Areas Covered in the Session:
- Regulatory requirements for excel spreadsheets
- Spreadsheet design considerations and validation methods
- Risk based evaluation and qualification of spreadsheets
- Documentation requirements
- Common FDA audit findings and solutions
Who will benefit:
The following individuals or disciplines will benefit from attending this Webinar.
- System owners and personnel who create or use spreadsheets in FDA regulated areas
- QA / QC managers, executives and personnel
- IT / IS managers and personnel
- Validation specialists
- Software quality reviewers
- Regulatory affairs and training personnel
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
We accept credit card, debit card, and PayPal.
Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
