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