About CTEP: the creators of RealWorld EDC
CTEP (Clinical Trial EndPoint) has developed it's product - RealWorld EDC - specifically for the collection of real life data in a real world setting. CTEP can build, validate, host and support the eCRF or provide access to eCRF builder software.
CTEP was established in 2002 from the pharmaceutical sector and now specialises in providing electronic data capture (EDC) software for observational studies.
CTEP has its headquarters and development centre in Ireland (Dublin), a location renowned for world-class software development. In 2010 global standards organisation CDISC awarded certification to CTEP; joining industry leaders Medidata Solutions, PhaseForward, Perceptive Informatics and a small group of others to achieve this.
RealWorld EDC demonstrably complies with industry requirements for security, data protection and information quality, including the FDA Code of Federal Regulation 21.11 and CTEP is registered with the European Data Protection Commissioner as a data processor since 2002.
We provide electronic data capture (EDC) for international and national studies, and our customers come from a wide range of sectors including pharma companies, institutions, biotech, nutrition and contract research organisations (CROs).
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"...CTEP were always willing to adapt the provided CRF and to solve problems immediately. Our customers were especially satisfied about the quick and competent support." - Nikola Hemlberg, Project Manager, JSW Life Sciences, Austria
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CTEP launches data capture system for newly released drugs
A Dublin firm, Clinical Trial EndPoint (CTEP), has launched an electronic data capture system for observation studies, where patients’ experiences of newly released drugs are recorded, allowing significant cost reduction. read more»
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CDISC ESUG Meeting May 2011
We presented a paper at the ESUG meeting in Brunel in May this year. read more»