>> Company News
Web site redesigned
East Research Consulting Co, Ltd (ReCon) is a full service Contract Research Organization (CRO)
ReCon has experience of preparation and conducting clinical studies phase I-III, screening research, pharmacy-economical research, and analytical services with a competitive speed and a competitive price.
Experienced and efficient study managers and monitors have the highest medical university degrees (MD), have GCP certifications, have vast experience in multicenter, randomized, double-blind clinical trials (include FDA-controlled studies), and are heavily involved in studies themselves, providing feed-back on study preparation, conducting, and reporting. Own staff participated in planning, management, conducting and monitoring studies of different indications such as arterial hypertension, HIV/AIDS, tuberculosis, asthma, mental disorders, multiple sclerosis, cancer uteri, breast cancer, diabetes mellitus and other. Because of high qualification and experience of personnel all tasks are solved quickly and flexibly.
We conduct all studies according to the specifications of internationally adopted guidelines and regulations, (such FDA guidelines, EC CPMP/EMEA, ICH and OECD guidelines, and local regulations), ReConís Policies and SOPs.
Due to presence of a wide database on investigators and sites, term from the beginning of preparation up to first patient enrolled is considerably reduced. Own database include more 550 sites in various therapeutic areas such as oncology, internal disease, cardiovascular system, respiratory system, neurology, dermatology, pediatrics, and more.
In the database there are data on quantity of investigators on each site, their experience of participation in researches, GCP compliance, and supply and laboratory capability of a site. We have an opportunity to give to you sites with the fastest enrollment and the highest quality.
Data in own database is updated and complemented constantly by Data Management Department which has large experience of SAS and others medical databases working.
ReCon has experience in Study Designs and Protocols writing; Investigator Brochures review and writing; CRFs designing and writing; ICH/GCP/ local regulations review of study protocols.