Analytical Method Development and Testing

At BioLink Lifesciences, we specialize in providing comprehensive Analytical Method Development and Testing services for the pharmaceutical and biotech industries. Our state-of-the-art Analytical Chemistry Laboratory is equipped with cutting-edge technology and staffed by experienced scientists who deliver high-quality results. Here’s how we can assist you:

Analytical Method Development

Our team tailors analytical methods to each stage of your drug development program. Whether you’re in early-phase clinical research or commercial production, we ensure efficiency, cost-effectiveness, and compliance with quality requirements. Our services include:

HPLC Analytical Method Development and Validation

– Assay determination
– Related substances analysis
– Dissolution testing

Cleaning Validation and Verification

– Ensuring equipment cleanliness and product safety

Pharmacopoeia Testing

– Testing raw materials and finished products according to USP/NF, EP, BP, JP, and client-specific methods

Proton NMR and Carbon-13 NMR Services

– Providing detailed structural information

Clinical Trial Support

– Method development and batch release for clinical trials

Elemental Analysis

– Determining carbon, hydrogen, and nitrogen content

Liquid Chromatography-Mass Spectrometry (LC-MS) Services

– Identifying and quantifying compounds

Infrared Spectroscopy Services

Method development and batch release for clinical trials

UV Spectroscopy Services

– Analyzing UV-visible absorption spectra

Detecting solvents in drug products

– Separating and analyzing volatile compounds

Residual Solvent Analysis

– Detecting solvents in drug products

Ion-Chromatography Services

– Analyzing cations and anions

Gas Chromatography Services

– Separating and analyzing volatile compounds

Lyophilization of Small Molecules and Biologics

– Freeze-drying for stability and preservation

Method Validation

Our team develops custom validation protocols based on parameters, processes, and acceptance criteria. We ensure compliance with ICH and FDA guidelines. Once methods are validated, we provide thorough reports suitable for regulatory submission.

Why Choose BioLink Lifesciences?

  • Expertise

Our scientists have extensive experience with diverse molecules, materials, formulations, and packaging configurations.

  • Regulatory Compliance

We adhere to ICH, GMP (Good Manufacturing Practice), and GLP (Good Laboratory Practices) standards.

  • Patient Safety

Our rigorous testing ensures safe and effective pharmaceutical products.