ASI works with clients who manufacture in FDA regulated environments, to validate systems, ensure quality, optimize processes, and achieve successful outcomes. Our consultants have an average of 20 years experience in life sciences manufacturing, quality systems, information technology, engineering, and regulatory affairs.
Contact ASI today to discuss your toughest technical and compliance challenges.
ASI is comprised of the following three groups:
Our compliance staff has experience with equipment, facility, utility, computer hardware/software, process, cleaning, and test method validation/qualification in FDA regulated environments.
We can provide seamless, plant-wide information architecture with visibility to all layers of the organization. Our engineers can deliver classical PLC, HMI, SCADA, and DCS design, development, and systems integration.
ASI has a large staff of engineering, life science, and computer science professionals, all of whom possess cGMP regulated industry experience and a proven track record of accomplishment.
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