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| Compliance & Validation Services | Integration Services | IT Services | Products | |||
FDA regulations on the use of electronic records and signatures, entitled 21 CFR Part 11 (or 'Part 11'),
came into force in 1997. The regulations are not specific to any type of instrument or technology, but
applies to all instruments, applications, and operations that save data electronically to any media.The Pharmaceutical and Healthcare industries arguably the most regulated industry sectors in the marketplace. read more... |
InnoPte builds, integrates and supports many different kinds of systems that conform to your business processes and
requirements. We can help you evaluate off-the-shelf systems for use within larger, custom built corporate systems, ensuring the entire enterprise level system is Part 11 compliant read more... |
InnoPte has been a strategic pharmaceutical software development partner for pharmaceutical companies ranging from
start-ups to Fortune 1000 companies. Our wide industry expertise in building robust, scalablesoftware for the pharmaceutical industry has helped InnoPTe to build a knowledge repository on pharmaceutical software needs and best practices. read more... |
Innova Analytical Data Management Tool (Innova ADMT):to capture ,distribute and analyze lab result data and provide means to generate customizable reports.
read more... |
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