Real World EDC is a software application designed by Clinical Trial EndPoint (CTEP) Ltd. CTEP started in 2002 and has established a global reputation as a specialist provider, supporting post marketing surveillance (PMS) studies. We offer an end-to-end solution from eCRF design and build, to the delivery of a clean set of data.
Our multidisciplinary team lies at the core of our unique software solution. We share extensive global pharmaceutical and IT industry experience, including deep insights into observational studies. Together, our knowledge and expertise is extensive and broad reaching. Learn more about our management team»
Over the past 10 years we have continually listened to our customer’s needs which has driven the evolution of a leading EDC system for PMS studies globally. RealWorld EDC makes Simple the collection and management of patient data for PMS studies.
We have worked with many world leading pharmaceutical companies across the globe. Our software first launched within Europe has proven success in Ireland, UK, France, Netherlands, Germany, Austria, Slovakia and Slovenia. We continue to expand our global outreach - our largest study to date was conducted in Russia. As a result the pharma sponsor made significant cost savings while the participating doctors reported a favourable experience with RealWorldEDC. RealWorld EDC is preparing to launch in Japan in 4Q 2016.
Our vision is to continue to advance PMS globally through market expansion.
We have two models for working with our clients:
- Providing Real World EDC directly to pharma and related sectors
- Partnering with contract research organisations (CROs) who use Real World EDC and promoting these CROs to pharma clients
CTEP has its headquarters and development centre in Dublin, Ireland, delivering service worldwide from this base. We operate a stable, successful and ambitious company that is ideally placed to be your partner in observational study data collection.
We would love to hear from you – contact us.