Stay informed
Centrally manage all your trials and clinical data. Automatically deliver real time updates to study managers from site and patient data.
Surface issues, automatically
Act on trial irregularities in real time with automated quality management. Monitor safety from the point of data capture through completion.
Be prepared
Have the flexibility to virtualize elements of your trial quickly, during COVID-19 and beyond.
Work efficiently and effectively
Access all your applications with a single sign-on (SSO). Connect disparate workflows in one system for a continuous and navigable work experience.
Save time
Automate document generation and site payments, eliminating duplicate work.
Improve collaboration
Create a secure, collaborative environment for sites and team members to work with the same data.
Centralize operations
Operate with a clear view of all your cross-application data in one place. Integrate with your existing data systems, eliminating manual data entry and reconciliation, while maintaining full control and oversight.
Simplify reporting
Customize reports within or across studies and leverage over 30 standard reports.
Standardize and improve data quality with powerful artificial intelligence and machine learning algorithms that automatically manage the complexity of clinical data for you.
Reduce complexity
5 days
to reach database lock
One place for your data
One place for your work
One place for your trial
80%
reduction in data correction rates
40%
reduction in edit checks
76%
of trial file master data can be populated automatically from Rave EDC and CTMS
60%
reduction in CRA time to reconcile the Investigator Site File (ISF) and the Trial Master File (TMF)
70%
reduction in time to create monitoring visit reports
$297K
cost reduction per study from minimizing on-site travel
30 Days
to pay sites
64%
reduction in study build time
1
2
3
2
Analysis by Medidata Value Team for customer with Rave EDC, Coder, and TSDV; 2018
1
Customer-sponsored value analysis for Rave EDC, Coder, RTSM, Detect, and TSDV; 2018
3
Analysis by Medidata Value Team for customers with Rave EDC, Detect; 2018
4
5
6
5
Customer-sponsored value analysis for Rave EDC, CTMS and eTMF; 2019
6
Customer-sponsored value analysis for Rave EDC, CTMS and eTMF; 2019
4
Customer-sponsored value analysis for Rave EDC, CTMS and eTMF; 2019
7
8
9
8
US Sites automatically paid within 30-days using Rave EDC and Site Payments together
9
Analysis by Medidata Value Team for customer with Rave EDC, Coder, TSDV); 2018
7
Analysis by Medidata Value Team for customer with Rave EDC, TSDV, eCOA, Coder, and RTSM; 2018
One place for your data
One place for your work
One place for your trial
One place for your data
One place for your work
One place for your trial
One place for your data
One place for your work
One place for your trial
Centralize operations
Operate with a clear view of all your cross-application data in one place. Integrate with your existing data systems, eliminating manual data entry and reconciliation, while maintaining full control and oversight.
Simplify reporting
Customize reports within or across studies and leverage over 30 standard reports.
Standardize and improve data quality with powerful artificial intelligence and machine learning algorithms that automatically manage the complexity of clinical data for you.
Reduce complexity
40%
reduction in edit checks
80%
reduction in data correction rates
5 days
to reach database lock
Work efficiently and effectively
Access all your applications with a single sign-on (SSO). Connect disparate workflows in one system for a continuous and navigable work experience.
Save time
Automate document generation and site payments, eliminating duplicate work.
Improve collaboration
Create a secure, collaborative environment for sites and team members to work with the same data.
76%
of trial file master data can be populated automatically from Rave EDC and CTMS
60%
reduction in CRA time to reconcile the Investigator Site File (ISF) and the Trial Master File (TMF)
70%
reduction in time to create monitoring visit reports
Stay informed
Centrally manage all your trials and clinical data. Automatically deliver real time updates to study managers from site and patient data.
Surface issues, automatically
Act on trial irregularities in real time with automated quality management. Monitor safety from the point of data capture through completion.
Be prepared
Have the flexibility to virtualize elements of your trial quickly, during COVID-19 and beyond.
$297K
cost reduction per study from minimizing on-site travel
30 Days
to pay sites
64%
reduction in study build time