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Clinical trials play a key role in the pharmaceutical, biotechnology and medical device industry. We have Data Managers, EDC Developers and SAS Programmers available around the clock. Regardless of EDC tool {Medidata Rave, Medrio, Oracle InForm, OpenClinica, Oracle RDC, Datatrak or others}; we strive to provide you the best service by implementing CDISC standards from initial development.

What others Clinical Research Organizations (CROs) consider 'Unique' pages, we consider them 'Standards'. Why? We have developed most CDISC standards forms in most {EDC} systems so there is no need to reinvent the wheel.

What you get? Quick turn-around, cost-effective setup. We can setup trials in less time than most CROs as we use libraries from CDISC standards. Our SMEs then can concentrate on 'Unique', 'Study-specific' or more complex CRFs as per protocol.

For further information, please Contact Us!

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Panama City
Panama

USA.: + 1786 408 7654
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UK.: + 44 84 5004 2983
service[at]raeclinica.eu

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