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Clinical Trial Design

Develop study-related protocols, case report forms (CRFs) and database tools for records management.
General Toxicology

Use in vivo models to assess acute and sub-acute toxicity as well as chronic and sub-chronic toxicity.
In Vitro Disease Models

Screen pre-clinical candidates without the use of live animals.
Quality Control

Ensure products or services adhere to a set minimum standard.
GMP Synthesis

Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
Plasmid DNA Preparation and Extraction

Prepare plasmid DNA starting from E. coli cell pellets, transformed colonies or DNA samples.
Large Scale Protein Production

Produce large amounts of protein using fermentors, wave mixers, bioreactors, and large-scale purification workflows.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Endotoxin Testing

Detect and quantify the presence of endotoxins from gram-negative bacteria.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
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