Created to address higher standards in pharmaceutical compounding, STAQ Pharma operates FDA-registered 503B outsourcing facilities that produce sterile compounded medications for hospitals and healthcare systems. Its facilities were built from the ground up to cGMP standards, with the original Denver site opening in 2018 and a much larger Columbus facility producing its first commercial batch in 2023. Backed and guided by healthcare systems, STAQ supplies medications nationwide while focusing on drug-shortage resilience and consistent quality.
FDA-Registered 503B Outsourcing Facility
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FDA-Registered and Inspected Facility
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DEA-Registered Facility
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cGMP Standards
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