Company Overview

Insite Quality Assurance, Inc. was founded in 2000 as a Biotech consulting and contract GCP audit vendor focused on providing quality assurance support to the biotechnology industry. Our key services are designed to facilitate clinical trials of biologics, small molecules and medical devices. As the development demands in our industry, and the intensity of FDA and EMA inspections, have grown so too has the demand for Insite QA expert compliance services. Our customers have sought our input and assistance in all GXP areas (Good Laboratory Practices, Good Manufacturing Practices, Good Computer Validation Practices, Good Tissue Practices, Good Documentation Practices) in all Therapeutic areas. To continue to support our clients we have added many other services; Technical Writing, GAP Analysis, Process and Systems Assessments, in addition to GMP, GLP, GTP and GCVP compliance audits to our portfolio of service offerings. Insite QA is a full service drug, biologics, medical device, nutritional supplements and veterinary quality contract vendor. Why Insite? Because we have the ability to place a qualified professional, on site, anywhere around the world, to fill urgent significant client needs.

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