ARL Bio Pharma is a contract laboratory that provides analytical and microbiological testing for the pharmaceutical industry. Since 1998, ARL has supported the industry-wide commitment to deliver high-quality drug products by providing guidance and test services for all phases of the product lifecycle following USP, FDA, and ICH guidelines. ARL works with health-systems, pharmacies, state boards of pharmacy, raw material suppliers, equipment manufacturers, and pharmaceutical manufacturers providing the testing needed to get drug products ready for release.
ARL Bio Pharma is an FDA registered and audited analytical laboratory and DEA licensed for Schedules I through V. The laboratory is ISO 17025:2017 accredited as applicable to our scope of accreditation. This ISO standard emphasizes ARL's ability to not only comply with quality requirements, but to competently perform specified tests and activities. measurements, and calibrations. This involves interlaboratory comparisons with products and materials of known composition or values, where ARL's performance is compared with a reference group. This provides additional tangible evidence of ARL's laboratory capabilities.