Pharmaceutical Manufacturing, Medical Devices and Bioinformatics
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Our offices are located in the Buffalo,
New York area, and we attempt to perform the bulk of the work here, close to home. However, most of us do travel to our clients' sites regularly
to provide some level of development on site. We typically do that anyway at the beginning of the project (during requirements definition, high
level design and any reviews) and at the end, when the integration task requires tight cooperation among all players. |
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Yes. Given a set of requirements, we can develop the test procedures necessary to validate the requirements, and perform all testing as well. |
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In the pharmaceutical manufacturing environment ASG can provide expertise in manufacturing control and e-signature (21 CFR 11) applications. We can also provide independent verification and validation (IV&V) where corporate policy or the FDA demands it. |
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ASG has been involved in several medical device projects from product inception through requirements specification, design, the review process, debugging and testing, 501K submission, clinical trials, and product validation. To a great extent we can provide help at the systems and engineering management levels as well, codifying pertinent documentation and developing standards, test procedures, and other documents as required by the regulatory process. ASG generally acts as an adjunct to your existing engineering resources, especially for those companies that do not have significant software development expertise in an FDA-regulated development environment. |
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