PORTLAND, OR--(Marketwired - Oct 28, 2015) - Cromos™ Pharma, an international full-service CRO is strengthening its message of being able to deliver unparalleled patient recruitment with a disruptive "No Patients = No Payments" initiative.
This approach takes the risk sharing model to a new level by structuring agreements with biotech and Pharma companies in a way that allows sponsors to pay for the results that Cromos™ Pharma has promised from the outset.
"This is not a gimmick," said Vlad Bogin, MD, FACP, Cromos™ Pharma's CEO. "We arrive at timelines and recruitment numbers by performing a very careful feasibility analysis of each study and only then put our money where our mouth is. However, when we are confident that we can get the study approved, initiated and conducted, we are willing to put our reputation and our finances on the line."
"With 'No Patients = No Payments' initiative Cromos™ Pharma makes itself accountable for each step of a clinical trial, from timely regulatory approval, to selecting only the recruiting sites and the number of recruited patients," added Andrey Tarakanov, MD, Cromos™ Pharma's Managing Director.
"Every CRO promises you the world. We are willing to be financially accountable for what we promise," concluded Dr. Bogin.
About Cromos™ Pharma, LLC
Cromos™ Pharma, LLC is a contract research organization (CRO) with operations in the post-Soviet space and in Eastern/Central Europe. The company provides a full spectrum of trial-related services which include regulatory approvals, medical writing, feasibility assessments, monitoring, project management and warehousing. Cromos™ Pharma is a privately owned company.
Ukraine, the eight largest European country by population, is an attractive location for sponsors conducting clinical research for a number of key reasons. Cromos Pharma has been successfully managing clinical trials in Ukraine since 2006. This article looks at just some of the benefits of locating your next study here.
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Are you a sponsor seeking to conduct clinical trials in the European Union but do not have a registered office in the European Economic Area? If so, in order to comply with the European Union Clinical Trial Directive, you are required to work with a Legal Representative registered in an EEA country.
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If you missed the live webinar “Where in the world should I locate my pivotal clinical trial?” you can now watch the recording by clicking here. The webinar hosted by the Society of Physician Entrepreneurs (SoPE) and Workforce Genetics features Cromos Pharma's CEO Vlad Bogin, M.D, FACP.