EDC is where trial activity is first recorded: every visit, procedure and adverse event. In most organisations that data is then exported to CTMS, safety and finance on a schedule. Cloudbyz EDC is built natively on Salesforce, on the same data model as Cloudbyz CTMS, Safety & Pharmacovigilance and CTFM, so a completed visit updates operations, an SAE is shared with the safety case, and earned amounts reach finance in real time. It is used by large pharma, global multinationals, biotechs, CROs and device companies.
|
Data in EDC |
Who needs it |
Why |
|---|---|---|
|
Subject visits and enrolment |
Clinical operations (CTMS) |
Site status, milestones, monitoring |
|
Serious adverse events |
Pharmacovigilance |
Expedited reporting within 7 or 15 days |
|
Completed visits and procedures |
Finance (CTFM) |
Site payments and accruals |
|
Queries and data status |
Data management and CRAs |
Cleaning and lock |
Across a large portfolio, the number of EDC exports and interfaces grows with every study. A shared data model gives one consistent flow from EDC to operations, safety and finance for every study, reduces the validation work for each new study, and means accruals and safety oversight across the portfolio are built on the same source data.
Biotechs need EDC live quickly and can't afford integration projects. Starting with Cloudbyz EDC and adding CTMS, Safety or CTFM later on the same platform means data flows to each new module without building interfaces, and a small team has one source of truth from the first patient.
Cloudbyz EDC is built natively on Salesforce, with a form builder, eCRFs, edit checks and query management. Because it shares a data model with Cloudbyz CTMS, Safety & PV, CTFM and eSource, completed visits update CTMS and create earned amounts and accruals in CTFM, SAEs can be shared with the safety case, and data captured once in eSource doesn't need to be re-entered. Book a demo or visit cloudbyz.com.