Pharmaceuticals summary

Exova's analytical expertise provides solutions

Exova has more than thirty years' experience providing high quality testing and development services to the pharma and medical device industries. We’re a medium-sized, highly flexible and adaptable team that values communication. Strong expertise and a wide range of instrumental capabilities allow us to provide one-stop integrated solutions.  Our teams work closely with you at every stage to provide tailored solutions, guiding you through the testing process, reducing your costs and, ultimately, helping you to close the gap between concept and launch.

We’re audited by more than one-hundred customers per year as well as various regulatory agencies which support our commitment to continuous improvement of our systems and procedures. Many of our relationships have lasted more than twenty years, and our data has contributed to faster development as well as successful approval of a wide variety of healthcare products.

A summary of our pharmaceutical testing and development services include:

  • Raw materials testing following USP/NF, EP, JP, FCC, ACS, and others
  • Finished product QC testing following USP/NF, EP, JP, FCC, ACS, and others
  • Analytical method development & validation
  • Analytical R&D Services
  • Regulated Substances testing
  • Low level radioactive materials testing
  • Materials analysis
  • Biological sample testing
  • Screens for metals, volatiles, semivolatiles, and more
  • Combination products and development
  • Extractable/leachable studies
  • Heavy Metals Testing by ICPMS per USP and EP
  • Medical device testing and development
  • NMR spectroscopy
  • Physical characterisation
  • Preformulation development
  • Polymer testing and plastics testing
  • Residual Solvents Testing per USP and EP
  • Stability studies

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