The drive towards Electronic Records and Signatures, combined with technological advances in networking, cloud computing, and virtualization, is inevitably changing how drugs and medical devices are manufactured. GxP Monitoring is changing in parallel to the evolving landscape of modern GxP manufacturing. It is critical that we understand this evolution so that we can select future-proof monitoring solutions.
This can be achieved through three major pathways:
1) Integration of multiple device inputs to maximize potential applications
2) Interoperability with other systems to ensure secure information exchange
3) Flexibility of process and system architectures to match the business and network landscape
This is the pathway to ensure that your monitoring system is adaptable now and in future, rather than at risk for obsolescence.
Join us for a one-hour webinar on how system integration and device interoperability can make environmental monitoring systems future-proof.
Paul Daniel is the Senior Regulatory Compliance Expert at Vaisala. He has worked in the GMP-regulated industries for over 20 years helping manufacturers apply good manufacturing practices in a wide range of qualification projects. His specialties include mapping, monitoring, and computerized systems.
At Vaisala, Paul oversees and guides the validation program for the Vaisala viewLinc environmental monitoring system. He serves as a customer advocate to ensure the viewLinc environmental monitoring system matches the demanding requirements of life science and regulated applications.
Paul also shares his GMP experience through regular blog contributions, webinars, and seminars around the world. Paul’s expertise in the demanding GxP world is applicable to any industry where measurement is critical to product quality. Paul is a graduate of University of California, Berkeley, with a bachelor's degree in biology.