CCR

	CCR - an independent Ukrainian company offering to customers wide spectrum of service in the area of clinical research
	founded in 2003 by the group of researchers with long-term experience in organization and management of clinical trials

	Ukraine is situated in the heart of Europe
	Ukraine has relatively large population
	relatively small numbers of studies are conducted in Ukraine
	a great number of perspective research centers is ready to participate in new projects
	world-wide pharmaceuticals companies and CROs open their representative offices in Ukraine

	CCR is a first Ukrainian company providing customers with full set of logistic services
	with the assistance of our partners CCR developed a logistic chainlet, beginning from the import of research preparations to Ukraine and concluding them an export or destruction
	four years of experience of CT conduct
	CCR successfully passes Customers audits
	CCR clients are world-wide pharmaceuticals companies and CROs
	individual approach to every single Customer and Project
	all of our employees participate in trainings on a regular basis
	CCR meets Ukrainian standards and international norms: GCP, GDP,GMP
	in our work we follow own SOPs and working instructions

	thorough and everyday control of all the procedures in logistic chain, as well as their quality performance
	speed-up of the procedures: RA approvals, customs clearance, decision making
	reduction of the customer’s time in CT organization covering logistics
	work with several companies (couriers, authorities, warehouse, sites) through one organization

	to make considerable contribution to development in the sphere of clinical trials in the world and in Ukraine as well
	maximally satisfy all Customer’s requirements and wishes
	to prevent all of possible problems, related to the features of CT conduct in Ukraine
	to perform effectively, qualitatively and rapidly
	to give a help in a decision any non-standard situations

	CCR offers a complete service: - receipt of licenses - import/export of CT materials and necessary equipment - storage, with the observance of necessary temperature conditions - distribution and delivery of clinical trial materials - realization of all procedures, related to destruction of the returned supplies - translation of medical and pharmacological documents
	all procedures are conducted in accordance with internal Standard Operating Procedures (SOP), Good Distribution Practice (GDP), Good Clinical Practice (GCP), Good Storage Practice (GSP) and Good Manufacturing Practice (GMP) and the relevant regulatory guidelines