Thank you for your interest in the Vaisala Validation Webinar Series

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Webinar #1 – What is Validation? 
  • This webinar covers the basics of validation
  • Overview of regulations that mandate validation
  • What is the role of validation within a larger Quality System?
  • Different types of validation in the pharmaceutical and medical device industries
  • Methodology and goals of validation
Watch Webinar #1

Webinar #2 –5 Rules for Sensor Placement in Validation/Mapping
  • How to deploy sensors in environmental mapping studies
  • How many sensors to use and where to put them
  • How to map controlled environments of all sizes, from table-top incubators to warehouses
Watch Webinar #2

Webinar #3 – Validation Protocols 

  • Specific types of data that are expected to be collected during a study
  • How to create validation protocols
  • How to review or approve such protocols
Watch Webinar #3

Check out all our webinars on Vaisala Webinar Central. 
Please click the links below to access the recorded webinars
Paul Daniel is the Sr. Regulatory Compliance Expert for Vaisala's Life Science segment. Paul has extensive practical experience in applying the GMP principles found in 21 CFR Parts 11, 210, 211, and 820. His specialties include: authoring and executing validation protocols (IQ and OQ) for pharmaceutical manufacturing and software validation with a risk-based approach drawn from GAMP guidelines.

Paul can be reached to answer your questions on validation/mapping at:
Webinar Instructor Paul Daniel
Learn more about Vaisala's validation/mapping solutions by contacting your local Vaisala representative here.

Or, call 800-408-9454 (International: +1 781 933 4500)
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