Preclinical and Clinical Technologies

Preclinical and clinical technologies pave the way for a novel compound to be developed as a safe and effective treatment.

Aptuit recognizes the importance of these critical steps and provides customers with an integrated network of global resources and an innovative management team experienced in all activities required for submission of a successful IND (exploratory or standard).

We ensure that your product moves beyond preclinical regulatory requirements and gets a significant head start to proof-of-concept and large scale clinical trials.


Our preclinical technology includes:-

 

  • Toxicology
  • Safety Pharmacology
  • Discovery Pharmacology
  • Drug Metabolism
  • PKPD
  • Bioanalysis

 

 Preclinical photo


Aptuit Consulting's regulatory group can support your pre-clinical program by preparing and managing your IND submission to the US FDA or your CTA submission in Europe. To find out more click here.