Quality
ARL Bio Pharma is a leader in analytical and microbiology testing for pharmaceutical drug products, raw materials, and biologics.
Ensure your products, personnel, and quality meet and exceed quality and compliance standards with our laboratory’s testing services
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Quality Management System
ARL Bio Pharma’s Quality Management System (QMS) meets all the requirements for testing laboratories, demonstrating our technical competence and ability to produce technically valid results. Our laboratories are accredited to ISO 17025:2017 and comply with the standards set by the FDA, ICH, and USP.
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Our Commitment
ARL Bio Pharma is committed to providing accurate and timely data to our customers and maintaining an organizational culture that promotes quality first, continuous improvement, and fosters personal and professional growth.
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Quality Programs
ARL Bio Pharma’s robust quality programs include audits, corrective and preventative action, change control, document control, impact assessments, data integrity, instrument calibration, IQ/OQ/PQ, external and internal quality control, emergency management systems, supplier qualifications, test method validation and quality control, traceability, and ongoing training.
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Accreditations and Certifications
ARL Bio Pharma is an FDA-registered and inspected laboratory specializing in analytical, chemical, and microbial analysis. We are registered with the DEA and the OBNDD, which enables us to handle Schedule I-V drugs, and we maintain our registration with the EPA and the Oklahoma DEQ. Our laboratories are accredited and inspected according to ISO 17025:2017 standards for chemical and microbial testing. Additionally, ARL Bio Pharma is registered and inspected by the Oklahoma State Board of Pharmacy as a drug wholesaler
More Info
If your facility would like to schedule an audit of our laboratories, contact info@arlok.com.
If you have questions regarding ARL’s quality accreditations and programs, contact info@arlok.com.