Safety pharmacology

You need a wealth of experience from your CRO. That experience must encompass the use of multiple species for regulatory safety pharmacology studies. It also needs to include efficacy evaluation of a wide variety of test materials. You’ve come to the right place. Envigo has experience across our entire organization at your disposal to support in-life phases of your study and a wide diversity of bioassay endpoints.

In fact, we have a long heritage in safety pharmacology. With more than 25 years’ experience, we are specialists in the performance of high quality in vitro and in vivo studies conducted to the highest ethical standards and tailored to meet regulatory and scientifically relevant endpoints.

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  • Cardiovascular
  • Respiratory assessment
  • Central nervous system
  • Electrophysiology
  • Follow-on studies
  • Supplemental studies

Additional services:

  • Efficacy
  • Bespoke study designs

Our team of Study Directors, analysts and technicians has an average of more than 10 years of experience in pharmacology in all the relevant areas of study design and testing.

The future of inhaled medications and inhalation technology

[Webinar] De-risking drug development: in vitro strategies that add value to your molecule