C.RIS PHARMA
Contract Research: the innovation at the service of your development
C.RIS Pharma, your contract research organization, dedicated to understanding your needs and offering you in vitro and in vivo studies tailored to your projects.
Our services are conducted in full confidentiality and in accordance with quality standards (GLP). Our R&D staff will work closely with you in developing new models for your therapeutic applications.
Scientific expertise for your research
C.RIS Pharma is committed to high quality services based on the expertise of its team and new facilities, a 1000 m² laboratory with specific containments for:
– Cell biology (P1, P2)
– Molecular biology
– Biochemistry
– Microbiology (P1, P2)
– Husbandry (A1, A2)
– Histology
– Analytical
– Access to MRI and cytometry
CORPORATE STRATEGY
Proximity
The close collaboration between our scientists and yours guarantees a rewarding and fruitful working relationship. Our project management is based on transparency with regular project reporting as frequently as requested.
Reactivity
We are focused on providing fast and efficient support in your drug development and on meeting your deadlines whilst still providing high-quality work.
Flexibility & Expertise
C.RIS Pharma’s strengths include the ability to develop individual solutions to meet your specific needs and to drive your projects forward with expert advice.
Contract Research: Our mission
At C.RIS Pharma, we advise you for:
– The evaluation of regulatory requirements, based on results and therapeutic application
– Design of complete programmes
– The monitoring of outsourced studies
– Preparation of scientific and regulatory dossier
– Risk assessment and safety evaluation
C.RIS Pharma will work hand in hand with you throughout the full non-clinical development of your product. (pharmaceuticals, medical devices, veterinary drugs, food products, chemicals, agrochemical, biocides, cosmetic…).
Quality assurance and confidentiality
From the outset, C.RIS Pharma has set out to be at the cutting edge of quality.
Our Quality-Assurance program guarantees that all Good Laboratory Practices (GLP) – declared studies are conducted according to the International standards of GLP since 2008 to ensure the generation of high quality and reliable test data.
Our Standard Operating Procedures (SOPs) are continuously updated and all study plans, critical study phases and reports are audited by our quality assurance staff. Protocols, data and reports are produced.
At C.RIS Pharma, the Quality and the Confidentiality are not only a commitment, but a state of mind shared by all the team.
