In this 45 minute training session, three industry experts explain why validation is not just a regulatory checkbox for 3PLs, but a practical tool to demonstrate operational control to pharma, medical device, and biotech clients.
In today’s evolving regulatory landscape, third-party logistics (3PL) providers are under increasing pressure to demonstrate full compliance across the pharmaceutical and biotech supply chain. From temperature-controlled warehousing to validated shipping environments, your clients — and regulators — expect more.
Join Performance Validation for this insightful session as we break down what validation really means for 3PLs. You’ll learn when and where temperature mapping is required, what regulatory bodies expect, and how to use validation as a competitive edge to win and retain life sciences clients.
In this webinar, you’ll learn:
Whether you're looking to secure new contracts, prepare for an audit, or strengthen your facility’s credibility, this webinar will provide the practical insight you need.
This webinar is conducted in cooperation with Performance Validation and the registration and participation information is shared with them. Please find their privacy policy.
Continuous Monitoring System for Controlled Environments and GxP Applications: Monitor Temperature, Humidity & Universal Input data loggers. Monitoring, alarming and reporting for GxP environments.
Ideal for stability chambers, refrigerators, freezers, incubators, warehouses, ambient environments and other demanding studies.
Understanding the critical process parameters of a controlled environments crucial to the safe and effective use of that space for manufacturing, storing, processing and distributing pharmaceuticals, biologicals, and medical devices. Vaisala mapping/validation service ensures that you fully understand the variability of conditions and qualify controlled environments.