Preclinical Drug Development

Our services in preclinical drug development include:

  • design and implementation of a fit-for-purpose preclinical drug development plan
  • design of preclinical studies, such as toxicology, pharmacokinetic and safety pharmacology studies
  • support in outsourcing preclinical studies and choice of CRO’s
  • monitor studies outsourced at a CRO
  • review of toxicological study reports provided by the CRO
  • getting you in contact with other specialists to answer questions outside our area of expertise
  • evaluation of preclinical dossiers
  • prediction of safe starting dose in First-In-Human clinical trials
  • support MABEL approach and PKPD model development