Cromos™ Pharma is a regional contract research organization (CRO) that specializes in biopharmaceutical clinical monitoring & outsourcing to Geоrgia, Belarus, Russia, Ukraine, Baltic States, countries of Eastern Europe and Israel. The company has been successfully managing Phase I-IV clinical trials, bioequivalence and observational studies since 2004.
Our business model is a product of the most validated Western solutions which are carefully tailored to local environments.
Cromos™ Pharma has a proven track record of rapid patient accrual and retention that often exceeds other geographies by a factor of 5.
As project managers, our "summa cum laude" MDs and PhDs don't just flawlessly adhere to a study protocol, they appreciate the science behind it. By choosing Cromos™ Pharma you get an invariable guarantee that your project will be handled by the "A-team".
In 2012 Cromos™ Pharma has adopted a fully integrated, cloud-based, virtual workplace model. This has allowed for seamless integration of all offices and employees, significantly increased the company's productivity and reduced its overhead.
Cromos™ Pharma’s industry-leading proprietary CTMS further increases company’s internal efficiency and performance and empowers sponsors by providing them with real-time access to operational, administrative and financial information about their studies.
Cromos™ Pharma's risk-sharing clinical development platform allows the sponsors to pay for performance and is our guarantee that the study timelines will be met. It also offers biotech, pharma and device companies with promising technologies several unique business partnership algorithms, including clinical research program conduct in exchange for equity or licensing opportunities. We invite interested pharmaceutical, biotech, and medical device companies to reach out to us for an in depth evaluation of potential strategic partnerships.
OCT Clinical Trials offers phase I-IV clinical research services such as clinical monitoring, clinical trials, preclinical studies, quality assurance, data management, and regulatory affairs.
Worldwide Clinical Trials employs more than 1,600 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. Founded by physicians committed to advancing medical science, Worldwide is out to change how the world experiences CROs – in the best possible way.
From Early Phase and Bioanalytical Sciences through Late Phase and post approval, we provide world-class, full-service drug development services. With infrastructure and talent spanning 60 countries, we execute predictable, successful studies with operational excellence. We never compromise on science or safety. We’re never satisfied with the status quo. We’re the Cure for the Common CRO.