ARL Bio Pharma is a contract laboratory performing analytical, microbiological, and stability testing for pharmaceutical manufacturers, raw material suppliers, and health systems. The hiring mix is heavily weighted toward research and junior-level roles, with active work on quality policy development, audit remediation (MasterControl coding errors), and chemical waste management—indicating internal focus on compliance tightening and operational refinement rather than new service expansion.
ARL Bio Pharma operates as a contract analytical laboratory serving the pharmaceutical industry since 1998. The company is FDA-registered and audited, DEA-licensed for controlled substances (Schedules I–V), and ISO 17025:2017 accredited. Services span raw material testing, stability studies, dissolution testing, drug product formulation development, analytical method validation, and regulatory support across all product lifecycle phases. The lab works with pharmaceutical manufacturers, equipment suppliers, pharmacies, and health systems, delivering results under USP, FDA, and ICH guidelines. Headquartered in Oklahoma City with 201–500 employees, the organization operates a compliance-driven business model where regulatory alignment and data integrity are core operational requirements.
Analytical and microbiological testing, stability studies, raw material testing, dissolution, drug formulation development, and regulatory support following USP, FDA, and ICH guidelines. FDA-registered, DEA-licensed (Schedules I–V), and ISO 17025:2017 accredited.
Oklahoma City, Oklahoma. Privately held since 1998, operating across the United States with no international hiring activity indicated.
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