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
NON CLINICAL & CLINICAL
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)
Pharmaceutical Development
