About Real World EDC – based on pharma experience
Real World EDC is provided by Clinical Trial EndPoint (CTEP) Ltd and draws on extensive pharmaceutical industry experience, including deep insights into observational studies.
CTEP was established in 2002 and since then it has established a strong reputation as a specialist provider supporting observational studies. Our services include eCRF design and validation, hosting and support.
CTEP has developed its unique software solution - Real World EDC - specifically for the needs of post-approval or observational study data collection. We have worked with many of the most highly regarded international pharmaceutical companies.
CTEP’s practical pharma experience has provided its deep understanding of what is needed to run these studies successfully. This is the basis for our focus on cost-effective, multi-lingual solutions that are easy to set up and simple to use and deliver study outcomes on time.
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
Ireland is a recognised world-class hub for software excellence, and CTEP has its headquarters and development centre in Dublin, delivering service worldwide from this base. We operate a stable, successful and well-funded company that is ideally placed to be your partner in observational study data collection.
Learn more about our management team»