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