Your challenge is:

Getting your new molecular entity on a fast track to market.
Adapting to constant changes in the regulatory and marketing environment.
Respecting your cost and resource constraints for R&D.
Being able to track many different projects, while keeping control of all of them.
Being everywhere at the same time!

We have one solution: CRDP

We combine efficiency and reliability with the latest technology
and a Pan-European Site Management Organisation (Clinville Ltd.)

to ensure optimal quality and timelines for our services and a continuous
transparency in the communication with the sponsor.

We offer a contractual guarantee that we will deliver within budgets
and on time - with penalties if we do not make the grade and a bonus
if we are ahead of the deadlines.

Our services are:

Strategy of development until market approval
Set op of panel of experts
Elaboration of study design
Protocol writing
Case report form creation
Set up of e-trials
Organization of drug packaging
Clinical trial authorizations
Investigator recruitment
Monitoring
Data management
Statistical analysis
Final study report writing
Publications
Presentations
Organization of scientific meetings
Marketing concept
Graphical work
Videos

CRDP Ltd.
au Poyet
CH-1866 La Forclaz
Switzerland

Phone: +41 79 279 80 77

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