Quincy MA, - May 7, 2024- At the BioTalk Conference near Boston, Phizzle, Inc., today introduced the industry's first Data Transformation Engine, a software innovation that makes it possible to harmonize data from different lab instruments into any standard LIMs — closing a major gap in data integrity for BioPharma manufacturers.
"Data harmony is the key to easily integrate data from any environmental or lab instrument into any standard LIMs. The demands of 21CFR require end-to-end data integrity — our Data Transformation Engine is a major step forward in digitizing what is today a very clunky and often manual process." — Michael Patrick, Phizzle's Chief Innovation Officer
Phizzle's Data Transformation Engine is a key feature of the company's software-defined architecture underpinning its Digital Air Series solution for GMP manufacturers. "The algorithm and other features powering our engine can take data from any device — whether it is an air particle counter or a zeta particle analyzer — and harmonize it specifically to the unique requirements of a specific LIMs," said Patrick.
In a software-defined architecture, activities traditionally done by hardware are carried out by software. As a result, Phizzle's solution is agnostic to the type of instrument used in the production of drugs. Phizzle is the only software-defined architecture in the world with a production use case at a top 5 pharma manufacturer.
According to Patrick, the instruments used in the production of drugs are based on hardware-centric architectures. "The data from instruments in use today is by and large inflexible and device-specific — our architecture gives customers the unique ability to transform data into what it needs to be for the customer's specific LIMs."
Learn more at www.phizzle.com
About Phizzle's EDGMaker Platform
Phizzle's EDGMaker is the world's first and only scientific instrument platform to centrally manage drug production data. Our technology is unlocking the manufacturing potential of the pharmaceutical industry by bringing data standardization, instrument automation, and FDA-compliant digital record-keeping to critical drug production.