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Method Development and Validation

Develop and validate methods for synthesis and scale up of drug candidates.
Particle Size Analysis

Measure particle size distribution and characterize particle size, porosity and composition.
GMP Synthesis

Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
Drug Product Stability

Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
Excipient Compatibility

Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
mRNA synthesis

Transcribe mRNAs in vitro and add modifications such as polyadenylation and guanine capping.
Nanoparticle Synthesis

Create nano-level structures with unique features.
Nanoparticle Conjugation and Functionalization

Modify biomolecules to enhance structure and function.
Liposomes

Create artificial spherical vesicles that can be used as a vehicle for administration of drugs.
Excipients

Acquire synthetic or natural inert components to formulate therapeutic agents.
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