Small Molecules

Small molecule drug development and manufacturing depend on analytical data at every stage. Pharmacopeial requirements, impurity limits, stability expectations and contamination control continue to evolve, and materials, methods, packaging and production environments must each be verified before a product reaches patients.

We provide analytical testing across the small molecule lifecycle, from raw material and compendial testing through method development and validation, impurity analysis, stability programs, microbiology, container closure integrity and facility monitoring. Our GMP laboratories help you confirm product quality and support regulatory submissions.