Abstract: Methods, computer systems, and computer storage media are provided for providing a third-party user HIPAA-compliant access to an electronic medical record system at a clinical site. A request for a clinical study participant list is received from the third-party user, and it is determined that the third-party user has viewing and access rights with respect to the clinical study participant list. The third-party user can select a participant on the clinical study participant list and access the participant's electronic medical record within the electronic medical record system. The electronic medical record is presented to the third-party user in a read-only view, and the third-party user is prevented from searching the EMR system for other electronic medical records.

Abstract: Methods are directed at utilizing a patient's electronic medical record (EMR) information accessed from a cloud, such as that used in Blue Button technology. Once the patient's EMR information is downloaded from the cloud, it is used to automatically determine if the patient is eligible to participate in a clinical trial. The EMR information of the patient is also utilized to determine if there is a potential drug-drug interaction from of the one or more medications the patient is prescribed to take. Furthermore, the patient's EMR information is used to identify any warnings and indications regarding the one or more medications the patient is prescribed to take. Notifications are then sent to a patient device and devices of those that have permission from the patient to receive such information, such as family members.

Abstract: Methods are directed at utilizing a cloud-based application for notifying a healthcare provider, such as a hospital or urgent care facility, that one or more patients from the healthcare provider qualify for clinical trial participation. A cloud-based application is also utilized for notifying one or more clinical trial sponsors, such as a university or pharmaceutical company, that one or more patients from one or more healthcare providers fulfill clinical trial eligibility. Furthermore, a cloud-based application is utilized for notifying one or more clinical trial sponsors that one or more patients of a second healthcare provider match the qualifications of one or more clinical trials, wherein at least one match was identified from a first healthcare provider.

Abstract: Methods, computer systems, and computer storage media are provided for providing a third-party user HIPAA-compliant access to an electronic medical record system at a clinical site. A request for a clinical study participant list is received from the third-party user, and it is determined that the third-party user has viewing and access rights with respect to the clinical study participant list. The third-party user can select a participant on the clinical study participant list and access the participant's electronic medical record within the electronic medical record system. The electronic medical record is presented to the third-party user in a read-only view, and the third-party user is prevented from searching the EMR system for other electronic medical records.

Abstract: Methods, computer systems, and computer storage media are provided for providing a third-party user HIPAA-compliant access to an electronic medical record system at a clinical site. A request for a clinical study participant list is received from the third-party user, and it is determined that the third-party user has viewing and access rights with respect to the clinical study participant list. The third-party user can select a participant on the clinical study participant list and access the participant's electronic medical record within the electronic medical record system. The electronic medical record is presented to the third-party user in a read-only view, and the third-party user is prevented from searching the EMR system for other electronic medical records.

Abstract: Methods, computer systems, and computer storage media are provided for providing a third-party user HIPAA-compliant access to an electronic medical record system at a clinical site. A request for a clinical study participant list is received from the third-party user, and it is determined that the third-party user has viewing and access rights with respect to the clinical study participant list. The third-party user can select a participant on the clinical study participant list and access the participant's electronic medical record within the electronic medical record system. The electronic medical record is presented to the third-party user in a read-only view, and the third-party user is prevented from searching the EMR system for other electronic medical records.

Abstract: Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient's electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.

Abstract: Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient's electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.

Abstract: Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient's electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.

Abstract: Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient's electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.