End to End Clinical Process

Real time data collection, cleaning, reporting and analysis

Many major Pharma companies are today finding that, given the historical way their clinical development landscape has been built over the years, they are faced with an inefficient architecture based upon multiple independent systems with, multiple potentially fragile interfaces.  This  clinical landscape is dated, complicated, expensive and slow. Any future integrated system will need to accommodate at least the following:

• Industry standards including CDISC
• Adaptive and non-adaptive, complex designs
• The need for faster design (set-up), greater data visibility throughout and rapid database lock
• eSource
• Data capture from remote geographies via unreliable communication channels

The Cmed Approach

Cmed has partnered with a number of companies to deliver a true best of breed solution, for all your clinical trial data requirements. Our approach to these end-to-end solutions allows data standards such as CDISC, to drive standard interfaces between key components e.g. CRF/database design and deployment, data capture and management, and real time analysis and reporting.