Are Your Production Systems Performing within your SOPs?

Controlling your process in the manufacture of your products to maintain accuracy and quality is crucial to the production of your products. Non-compliance with the standard operating procedures, cGMP guidelines, and FDA regulations can delay product production, costing you time, money, and reputation.

Masy BioServices' validation services group qualifies your critical life science research and production equipment and environmental storage chambers, ensuring the highest possible quality of product development and delivery.

Our turn-key solution includes:

• writing installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) protocols.
• executing validation protocols.
• a thorough quality review of the final documentation.

With our large, dedicated validation team and one of the largest fleets of validation equipment available, we can confidently meet or exceed your time frame requirements without sacrificing quality or accuracy. Masy's skilled professionals can perform multiple chamber or equipment qualifications simultaneously using multiple datalogging systems, saving you precious time and money with minimal disruption to your production cycle schedule.