BioLink Life Sciences
Independent contract research organization (est. 2001) providing analytical chemistry, medicinal and synthetic chemistry, formulation and pre-formulation, topical product testing (IVRT/IVPT), stability storage and testing, and FTE-based project delivery. Operates cGMP-compliant analytical laboratories supporting method development, validation, compound synthesis and regulatory-compliant testing for pharmaceutical and biotech sponsors.
Industries
Nr. of Employees
small (1-50)
BioLink Life Sciences
Patents
Products
Chemical catalog (research reagents and reference compounds)
Catalog of molecules, impurities and analytical standards with identifiers available for inquiry and custom supply.
Custom synthesized molecules (mg to kg)
Custom synthesis and scale-up of novel compounds to support discovery, preclinical and clinical programs.
Chemical catalog (research reagents and reference compounds)
Catalog of molecules, impurities and analytical standards with identifiers available for inquiry and custom supply.
Custom synthesized molecules (mg to kg)
Custom synthesis and scale-up of novel compounds to support discovery, preclinical and clinical programs.
Services
Chromatography and spectroscopy method development, instrumental analysis, method validation and regulatory reporting for discovery through commercial stages.
Design and conduct of in vitro release tests and skin permeation studies using vertical Franz diffusion cells for formulation profiling and comparative studies.
Custom synthesis (mg–kg), route scouting, analog library synthesis, lead optimization, impurity and isotope-labeled standard synthesis, process development and technology transfer.
Immediate- and modified-release solid dosage and liquid/semi-solid prototype development, formulation optimization and scale-up support.
Polymorph screening, hygroscopicity, particle characterization, solubility profiling, pKa/partition coefficient determination, dissolution studies and excipient compatibility testing.
Environmental chamber storage and execution of real-time and accelerated stability studies across ICH climatic zones with data-driven reporting of physical, chemical and microbiological attributes.
Chromatography and spectroscopy method development, instrumental analysis, method validation and regulatory reporting for discovery through commercial stages.
Design and conduct of in vitro release tests and skin permeation studies using vertical Franz diffusion cells for formulation profiling and comparative studies.
Custom synthesis (mg–kg), route scouting, analog library synthesis, lead optimization, impurity and isotope-labeled standard synthesis, process development and technology transfer.
Immediate- and modified-release solid dosage and liquid/semi-solid prototype development, formulation optimization and scale-up support.
Polymorph screening, hygroscopicity, particle characterization, solubility profiling, pKa/partition coefficient determination, dissolution studies and excipient compatibility testing.
Environmental chamber storage and execution of real-time and accelerated stability studies across ICH climatic zones with data-driven reporting of physical, chemical and microbiological attributes.
Expertise Areas
- Analytical chemistry and method validation
- Topical product testing (IVRT/IVPT) and skin permeation studies
- Medicinal chemistry and custom compound synthesis
- Formulation development and pre-formulation
Key Technologies
- High-performance liquid chromatography (HPLC)
- Liquid chromatography–mass spectrometry (LC-MS)
- Nuclear magnetic resonance (1H/13C NMR)
- Infrared and UV-Visible spectroscopy