Description
ARL Bio Pharma is a contract laboratory providing comprehensive analytical and microbiological testing services for the pharmaceutical industry. The laboratory adheres to USP, FDA, and ICH guidelines and supports all phases of the product lifecycle. Registered with the FDA, accredited to ISO 17025, and licensed by the DEA for Schedules I through V, ARL Bio Pharma services a wide range of clients, including compounding pharmacies, outsourcing facilities, health system pharmacies, pharmaceutical manufacturers, raw material suppliers, and dietary supplement companies.
Services include:
– Accelerated Stability Studies
– Analytical Services
– Assay Development
– Bioanalytical Services
– Biological Testing
– Chemical Analysis
– Chemistry (CMC)
– Medicinal
– Chiral Separations
– R&D
– Chromatography
– Manufacturing
– Contaminant Analysis
– Dissolution Testing
– Efficacy Testing
– Endotoxin Testing & Removal
– Environmental Monitoring
– Excipients
– Expert Testimony
– Testing
– Feasibility Studies
– Filtration
– Forced Degradation Studies
– Gene Therapy & Testing Protocols
– In Vitro Testing
– Lot Release Testing
– Mass Spectrometry
– Materials Analysis
– Process Development
– Microbiological Control Services
– Microbiological Testing
– Mycoplasma Testing
– Particle Characterization
– Particle Size Analysis
– Pharmacodynamics
– Pharmacogenomics
– Pharmacokinetics
– Pharmacology
– Physical Testing
– Polymerase Chain Reaction
– Preclinical Testing
– Preclinical Testing Formulations
– Process Validation Studies
– Quality QA/QC
– R&D Services
– Raw Materials Analysis
– RNAi Technology
– Stability Studies
– Stability
– ICH
– Sterility Testing
– Toxicology Services & Analysis
– Transdermals/Transmucosals
– UV-VIS Spectrophotometer Analysis
– Validation
– Cleaning Equipment
– Vitamin Analysis
– Water Testing
– Wet Chemical Analysis
– Regulatory Services
ARL Bio Pharma continues to be a trusted partner in the pharmaceutical industry, demonstrating commitment to quality and compliance. For more information, please visit arlok.com.
Capabilities
- Accelerated Stability Studies
- Analytical Services
- Assay Development
- Bioanalytical Services
- Biological Testing
- Cell and Gene Therapy
- Chemical Analysis
- Chemistry (CMC)
- Chiral Separations
- Chromatography
- Cleaning Equipment
- Contaminant Analysis
- Contract Development and Manufacturing (CDMO)
- Dissolution Testing
- Endotoxin Testing & Removal
- Environmental Monitoring
- Excipients
- Feasibility Studies
- Filtration
- Forced Degradation Studies
- ICH
- In Vitro Testing
- Lot Release Testing
- Mass Spectrometry
- Materials Analysis
- Medicinal
- Microbiological Control Services
- Microbiological Testing
- Mycoplasma Testing
- Particle Size Analysis
- Pharmacodynamics
- Pharmacogenomics
- Pharmacokinetics
- Pharmacology
- Physical Testing
- Polymerase Chain Reaction
- Preclinical Testing
- Process Development
- Process Validation Studies
- Quality QA/QC
- Raw Materials Analysis
- Regulatory Services
- Research & Development
- RNAi Technology
- Stability Studies
- Sterility Testing
- Testing
- Toxicology Services & Analysis
- Transdermals/Transmucosals
- UV-VIS Spectrophotometer Analysis
- Validation
- Vitamin Analysis
- Water Testing
- Wet Chemical Analysis
Contact Information
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