Pharmaceutical

Smithers offers a comprehensive range of pre-clinical and clinical services for all phases of drug development, including support for development of drug delivery devices, and medical and pharmaceutical packaging testing.

Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP- and GCP-compliant laboratories.

We conduct environmental risk assessments/environmental assessments to support registration in the EU and US for our pharmaceutical clients.

Smithers also offers accredited, third-party auditing and certification to the ISO 13485 quality management system standard for the medical device industry.