Vanishingly few clinical trials have a comprehensive and automated flow of information across their project. Yet site activity information is vital to accurately inform a demand-driven supply chain. Instead, paper-trails, key individuals, spreadsheets, and isolated databases dominate. Managing, collating and analysing the information costs money and introduces risk to the trial supply chain.
Many companies find the flow of information so fragmented and slow that the supply chain necessitates large safety stocks and significant project management resource.
IXR systems (both IVRS and IWRS) solve this problem by providing clinical trial control and reporting to automate the progress of subjects and IMP through the trial. These systems also provide real-time information for trial managers and decision support.
HMD clinical provides a solution for your specific study requirements, synchronising your data with your operations and eliminating wasted effort and risk from your information infrastructure.
For further information, or to arrange a demonstration of HMD clinical's systems, email us at info@hmdclinical.com
