The know-how you need
CapEval Pharma was founded in
2010 by Dr. Olivier Loget, DVM, ERT and provides pharmaceutical consultancy
services from early pre-clinical to clinical development, specifically in the
sectors of Safety, Toxicology, Pharmacology, Ophthalmology, ADME/PK, analytical
development, QA, CMC-Regulatory Affairs and Compliance. In addition, CapEval
provides expert assessment for due diligence, veterinary drugs, cosmetics,
agrochemicals and chemicals as well as staff training.
- Drawing on over 60 years of combined international experience, CapEval Pharma is a team of highly qualified pharmaceutical consultants, fluent in three languages.
- We provide scientific advice and training to identify the best approach to move your projects quickly through development and onto the commercial market.
- With experience working in Biotech, Pharma and CRO sectors, we are uniquely qualified to offer complete outsourcing management services for critical studies and product development.
- We have extensive experience in due diligence proceedings (> 100) providing expert assessment of both in- and out-licensing programs and creating gap analysis, which can be used for determination of project value.
- We have broad expertise in public subvention dossier, fundraising (Crédit Impôt Recherche etc) and medical writing.
- We work closely with clients, to help manage key objectives and make an appropriate assessment of regulatory hurdles taking into consideration the evolving requirements of the international regulatory landscape.
>100 Due Diligence projects in big pharma and biotechs
6-8 projects per year for in- or out-licensing
>60 years of combined international experience