Research into investigator dissatisfaction ("Investigator Dissatisfaction with the Conduct of Clinical Trials." Glass H. The Monitor August 2009) has identified some common issues that an IXR can address, helping you to complete clinical trials of high quality in a timely fashion.
- Managing site finances
- Too much time spent by CRA at site
- Managing clinical trial supplies
A well designed IXR can significantly mitigate these problems, reducing the cost of your trial and reducing the time needed to enrol subjects and reach database lock. HMD clinical's Pulse application can:
- Track site milestones (Site Activation, Subject visits, Shipment acknowledgements, etc) and automatically generate proforma invoices. Project Managers can authorize payments online. Investigators can monitor pending and authorised payments in real time.
- Provide the CRA with up to date pre-poulated documents and forms minimizing the on-site time by structuring the monitoring visit workflow more efficiently. For example – a drug accountability report to check the site supplies against is far more efficient than a blind stock check of the pharmacy.
- Manage the tracking and fulfilment of site supply requirements and substantially automate the generation of pharmacy storage, dispensation, returns and destruction logs to minimize workload.