The Data Trustees.
With 10 years of experience, the Trusted Third Party of the University Medicine Greifswald supports medical research in Europe. Person-identifying data are sensitive information. Therefore, it’s extremely important to protect access to this data – this is especially true for research with patient data in studies and registries. The organisationally Independent Trusted Third Party develops and operates specialised software to protect this data and, thus, offers data protection compliant solutions for medical research. As data trustees, we form the bridge between study participants, researchers and project partners and, thus, create trust, because: Trust makes medical research successful.
Are you planning storage and use of personal data for a study or a research project in compliance with data protection regulations? Are you looking for tools to help you with the digital acquisition and automatable processing of research data?
Are you a participant in a study, or do you plan to participate in a study? Did you receive an invitation to participate in a study? Would you like to inform yourself about the storage and use of your data?
Are you involved in conducting a study? Are you looking for documentation, e.g. descriptions of processes and standard operating procedures (SOPs)? Do you need access (login) to the data collection system of your project and search for the corresponding application?
The Trusted Third Party in numbers
As of October 2022
TTP-MedDocs and data managers strongly represented at DVMD congress
Science creates knowledge? In the TTP, everyone creates knowledge! At the DVMD anniversary congress in Leipzig, the TTP was strongly represented. But this time, the data managers and medical documentalists were on the scientific stage and in the spotlight for two days. All six colleagues who submitted an abstract [...]
New Community-Releases of E-PIX, gPAS und gICS available
Since today, updated releases of E-PIX, gPAS and gICS are available for download for the broad community. Besides new functionalities and numerous improvements, updated manuals and interface specifications are available. Part of the new community releases of E-PIX and gICS is a flexibly configurable notification system (notifications), e.g. to [...]
Great international interest in the new standard for patient consent based on HL7 FHIR®
We just finished our session on "Patient consent management in medical research with FHIR" at this year's FHIR DevDays 2022 in Cleveland, Ohio.The aim was to present the results of the HL7 Germany working group "Consent Management" and to make them known internationally. Of course, reference was also made to [...]
HL7 FHIR DevDays 2022: Patient consent management in medical research
Next week, the HL7 FHIR DevDays will take place in Cleveland, Ohio, as a hybrid event. The German HL7 FHIR Working Group "Consent Management" will present the freshly balloted FHIR Consent Profiles in the slot "Patient Consent Management in medical research with FHIR". These concepts form the basis for [...]
Live-Demo: Presentation of the new integration module for gICS in Thieme’s E-ConsentPro
Inspired by the MIRACUM sites and coordinated by the site situated in Dresden, Thieme Compliance has expanded its "E-ConsentPro" product to transmit consent content directly to the gICS consent management service in recent months. The technical basis for the connection is the freely available SOAP-interface of gICS. For the [...]