With Healex TrialFinance, the lack of transparency in the billing of clinical trials is a thing of the past.
Creating an invoice for a milestone within a clinical trial is very complex because each trial has different milestones. This does not fit with the process of patient-oriented billing, where each service has a fixed fee.
Clinical studies are different. This often leads to:
- The hospital receives a billing overview from the study partner;
- That an employee at the hospital (often the study coordinator) keeps a large number of Excel spreadsheets in order to keep track of when which invoice was issued and which items were included;
- External services are often forgotten to be invoiced.
Healex TrialFinance provides a transparent overview of services to be billed
With Healex TrialFinance, intransparency is a thing of the past. With TrialFinance, we allow the clinic to create an overview at any time of when which service was billed and how. At the same time, external service providers can acknowledge their services. This means that the trial center also has the respective departments and external service providers:
- Always an up-to-date overview of which services have been provided for the respective study;
- The departments can use the reporting to track which milestones still need to be reached in order to issue an invoice
- The invoice is created automatically as soon as the study coordinator has approved the items.
With Healex TrialFinance, the hospital increases productivity and at the same time the services provided are invoiced transparently. Here too, the solution is GDPR-compliant and offers coordinated roles and rights management, including an invoice approval process.
For more information, please contact our sales department.
Führende Kommunikationsplattform
für den Informations- und Datenaustausch zwischen Ärzten und Forschern in klinischen Studien
Multizentrisches Informations- und Datenmanagement System
für klinische Studienzentren, koordinierende Zentren und Forschungsnetzwerke
Zentrales Personenregister
aller an einer Studie beteiligten Prüfgruppen und Forscher mit Zugriffsbeschränkung durch Rollen- und Rechtemanagement
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