Préclinique et Clinique

PRÉCLINICAL (Pharmacology, toxicology, safety pharmacology)

With our partner

  • Consulting on preclinical activities programs
  • Set up and studies performing
  • Preclinical studies management
  • Audit, analysis and synthesis of research files for development candidates
  • Synthesis report writing of toxicology and safety pharmacology studies
  • Non Clinical Summaries and Non Clinical Overviews (CTD format)
  • Ecotoxicology studies programs


With our partner

  • Scientific and medical writing
  • Design and implementation of non-clinical and clinical parts of the dossiers
  • Clinical development plans and protocols
  • CTD format Summaries and Overviews
  • Risk Management Plans (RMP)
  • Periodic benefit risk evaluation reports (PBRER)
  • Notes of therapeutic interest (French Commission of Transparency)
  • Scientific communication tools (abstracts, posters, manuscripts, slide sets)