Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar

Join us for a webinar on Febuary 16 for a discussion of the webinar.

Who Will Benefit

  • All Excel users
  • IT
  • QA
  • QC
  • Laboratory staff
  • Managers
  • Executives

Webinar Takeaways

  • Develop spreadsheet applications that are GxP compliant
  • Learn how to use Excel’s built in 21 CFR Part 11 features
  • Apply features required for GxP environments without programming macros.
  • Follow along as we configure Excel for audit trails, security features, data verification, and multiple concurrent users
  • Validate your application with minimal documentation
  • Understand what does and does not need to be validated.
  • How to specify and test your application
  • Avoid 483s and Warning Letters
  • How to use cell and file protections
  • Reduce validation time and costs
  • Increase compliance while lowering resource needs

Overview

which explains how to configure and validate a GxP compliant spreadsheet applications to avoid FDA 483s. Follow the step-by-step instructions as we configure Excel for audit trails, security features, and data entry verification. David Nettleton will make you understand how to validate your application with minimal documentation. Bring your laptop and use Excel for your own needs. This session will make you a better Excel user, saving you time and costs

Industries who can attend

This 90-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.


Faculty David Nettleton

Faculty David Nettleton

Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, EU General Data Protection Regulation (GDPR), software validation, and computer system validation. He is involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications. He has completed more than 300 mission critical laboratory, clinical, and manufacturing software implementation projects. His most recent book is Software as a Service (SaaS) Risk-Based Validation With Time-Saving Templates, which provides fill-in-the-blank templates for completing a COTS software validation project. 

Choose a Purchase Options

$199

Live Webinar - Single Participant 90-mins

You get one log-in for the live 90-minute webinar for one participant, presentation materials and the opportunity to ask questions by phone and email

$399

Group Up to 5 Participants

You get 5 log-in for the live 90-minute webinar for all the participant, presentation materials and the opportunity to ask questions by phone and email


$299

Recorded Access Corporate Group

You'll have access to group log-in for an archived recording of the entire 90-minute webinar, including the Q&A period, for 1 location. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

$389

MP3 Download - Training DVD

Within 48 hours delivered - Lifetime Access ,Audio recording of a webinar and reference manual delivered by download. Listen anytime on any compatible device.

$289

Live + Recorded Access - Single Participant

You get one log-in for the live & recorded 90-minute webinar for one participant, presentation materials and the opportunity to ask questions by phone and email