摘要:
A method is for verifying the feasibility of a medical study using acceptance criteria for patients. The method includes defining target criteria for the study. Based on the acceptance criteria, a patient collective including potential patients is selected from a database containing patient data of patients. The patient data of the patient collective are evaluated based on the target criteria. Finally, a measure for the feasibility of the study is established.
摘要:
A method is proposed for determining clinical study compliance. The method includes obtaining criteria for the clinical study and accessing stored clinical data relating to the clinical study. Thereafter, the criteria and clinical data are correlated to determine a measure of compliance with the criteria of the clinical study.
摘要:
A method is disclosed for conducting a clinical study according to which an event occurs during the study that requires a collaboration of individuals responsible for the study. The method includes transmitting the event to a collaboration system. The collaboration system determines, based on parameters assigned to the event, a group of individuals responsible for the study required for the collaboration. The collaboration system provides a communications platform for the group. The group carries out the collaboration while using the communications platform. Finally, the collaboration system verifies the collaboration on the basis of predetermined verification criteria.
摘要:
A method is for obtaining medically relevant data from the gastrointestinal tract of a patient (human or an animal). The patient is orally administered with a transponder and signals emitted by the transponder during or after passage through the gastrointestinal tract are received, with the aid of a reading device for example. A measuring probe may be suitable for carrying out the method. The probe is designed as a transponder and includes a sensor unit for recording chemical, electrochemical or physical parameters.
摘要:
A method is proposed for examining a plurality of sites for a clinical trial. The method includes obtaining criteria for clinical trial and determining, using a computer device, how information regarding each of a plurality of clinical trial sites relates to the obtained criteria. Based upon the determinations, a plurality of the clinical trial sites are ranked. Thereafter, the ranked clinical trial sites may be reported to a sponsor of the clinical trial, and payment may be received.
摘要:
A method is proposed for determining clinical study compliance. The method includes obtaining criteria for the clinical study and accessing stored clinical data relating to the clinical study. Thereafter, the criteria and clinical data are correlated to determine a measure of compliance with the criteria of the clinical study.
摘要:
A method is proposed for determining clinical study compliance. The method includes obtaining criteria for the clinical study and accessing stored clinical data relating to the clinical study. Thereafter, the criteria and clinical data are correlated to determine a measure of compliance with the criteria of the clinical study.
摘要:
A method is proposed for determining clinical study compliance. The method includes obtaining criteria for the clinical study and accessing stored clinical data relating to the clinical study. Thereafter, the criteria and clinical data are correlated to determine a measure of compliance with the criteria of the clinical study.
摘要:
A method is disclosed for carrying out quality control of medical data records collected from different but comparable patient collectives within the bounds of a medical plan. In the method, for each data record, a quality control parameter assigned thereto is determined in the same manner. Further, the quality control parameters are evaluated using comparison criteria.
摘要:
A method is proposed for monitoring participation of a patient in at least one clinical trial. The method includes collecting data regarding at least one clinical trial for the patient. Using a computer device, the collected data is then compared to at least one threshold. Finally, the patient is rewarded upon the collected data at least meeting at least one threshold.