Webinar: Validation Expertise in GxP Environments

Register now to develop your validation expertise in GxP-regulated Environments.

 

Validation, qualification, verification activities are all about bringing data, proving that every component or process in your system will do what it’s designed or implemented to do, as desired, as expected, every time.

 

In pharmaceutical, biotech, and medical device industries, validation activities confirm that a system or process consistently achieves its objective. Validation safeguards the final product, the intended supply chain, and public health.

 

Global regulations, standards and guidance are freely available and read by almost anyone involved in quality control and assurance in life science industries. But regulations and standards are essentially ideals and objectives. They don’t tell you how to solve real world challenges, they don’t provide “how to” directions, and they can’t account for technological advances coming at an increasing rate.

 

In this webinar, Vaisala’s Senior Regulatory Expert Paul Daniel is joined by Axis Consulting principal Josh Keenan. Together, they will answer your questions on how to bring the data in GxP-regulated environments.

 

When: Thursday, 16 June 2022 12AM Australia Eastern Daylight Time (Sydney, GMT+10:00)

 

How to join: Find out how to register below.

Can’t make the scheduled time? Send your questions by email and register to receive the recording of the complete webinar.

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Find out more about the range of instruments that can be used for data validation activities.

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