User Acceptance Testing

This product is currently out of stock and unavailable.


Current regulations expect that all users are appropriately trained and that must include being trained how to effectively perform UAT.
This course provides an understanding of the role of users in system validation and covers good documentation practice and the writing of UAT scripts. It then moves on to running UAT scripts and the need for accurate reporting their results plus the implications when a stage in
a UAT script fails and program changes are necessary.
ICH GCP and 21 CFR Part 11 both expect that all computerized systems in clinical research should be validated, and the implementation of such computerized systems is growing exponentially. The process of establishing a computerized system is dependent upon one pivotal role – the User. The role of the User especially with regard to the User Acceptance Testing (UAT) is essential, but if users are not trained in all the areas that they need to be aware of when performing UAT the final system when implemented may not be as effective as it could have been.

Areas to be Covered:

Regulatory background
The validation process and where users fit in
The importance of documentation
User Acceptance Testing (UAT)
Writing UAT Scripts
Running UAT Scripts

Who will Benefit:

Clinical Research Professionals
Data Managers
Anyone who interfaces with a validated clinical system

Jane Tucker

Jane Tucker :
Over the past 28 years Jane has moved from routine data cleaning activities, via computer system validation onto training and data quality activities, eventually specializing in Quality Risk Management. Jane has worked for a variety of large pharmaceutical companies and CROs before retiring from GlaxoSmithKline. Jane now operates as a Risk Management Trainer and Consultant, specializing in Study Level Risk Management and Risk Based Monitoring as well as facilitation of risk assessment workshops.

Sue Fitzpatrick :
Sue Fitzpatrick joined the Pharmaceutical Industry in 1980. She has been responsible for the management and audit of CRAs and clinical trials in a wide range of therapeutic areas. As former Head of Education and Training at the Institute of Clinical Research she was responsible for the provision of training courses for the industry and postgraduate courses in collaboration with several UK Universities.

Sue continues her collaborations and is an accredited teacher with Cranfield University. Sue is currently a Director of Redtree people working on employability skills to help new entrants enter the sector. She has authored many articles and books on clinical research and career development topics. Sue is currently working on a book in Clinical and Healthcare Research for publication with the Oxford University Press.

This product is currently out of stock and unavailable.

  Go PRIME   🛈 $ 240 SELECT
  Personal Plan 🛈 $ 3000 SELECT
  Business Plan 🛈 $ 9000 SELECT

  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance