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Our work

We can review, design, change, verify changes, validate processes, train employees, and audit in the realm of quality systems, quality procedures, standard operating procedures for federally regulated and ICH and ISO guided pharmaceutical and medical device businesses.

Our final product is the delivery of concise, consistent and audience-friendly documents that are usable by everyone in the business, that are understood by high-level managers, and that are accepted by the auditors/inspectors. Benefits include simplicity of use and efficiency, and a comfort zone for managers to track progress of the projects.

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