full service CRO Phase II - IV, Clinical Investigations for efficacy, Clinical Investigations for safety, Clinical Investigations for pharmacodynamics, Pharmacoepidemiological studies, Consumer health studies, Pharmacoeconomics, Product profiling
Graphics, video, Film, communication design, Interactive programs, DVD, Case report form creation, Set up of e-trials, Organization of drug packaging.
Helps you strategize and maximize your clinical product development. 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 Research and Development. 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 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