Abstract: A system and a method for managing a clinical trial of patients. The method includes obtaining consents of the patients undergoing the clinical trial and storing consent data of the patients. Consent data of the patients is validated before progressing onto any stage of the clinical trial. Data associated with at least one clinical trial site is collected for performing the clinical trial. The patients are randomly grouped into two or more groups for performing one or more of a single blinded study and a double blinded study during the clinical trial. Clinical data and non-clinical data of the patients is collected during the clinical trial. Timelines, progress, compliance, and data associated with different stages of the clinical trial are managed.

Abstract: A system and a method for managing a clinical trial of patients. The method inlcudes obtaining consents of the patients undergoing the clinical trial and storing consent data of the patients. Consent data of the patients is validated before progressing onto any stage of the clinical trial. Data associated with at least one clinical trial site is collected for performing the clinical trial. The patients are randomly grouped into two or more groups for performing one or more of a single blinded study and a double blinded study during the clinical trial. Clinical data and non-clinical data of the patients is collected during the clinical trial. Timelines, progress, compliance, and data associated with different stages of the clinical trial are managed.

Abstract: Systems and methods for collecting clinical trial data across multiple locations is described. One described method; decentralized clinical trial design; comprises collecting clinical and non-clinical data on a client device over a network; the data is collected at a hospital, home or an alternate care facility, by either the patient or the healthcare professional; and transmitting the data, for access to sponsors over the network.

Abstract: Systems and methods for collecting clinical trial data across multiple locations is described. One described method; decentralized clinical trial design; comprises collecting clinical and non-clinical data on a client device over a network; the data is collected at a hospital, home or an alternate care facility, by either the patient or the healthcare professional; and transmitting the data, for access to sponsors over the network.

Abstract: Systems and methods for collecting clinical trial data across multiple functional modules is described. One described method comprises managing clinical and non-clinical data on a client device over a network; the data is linked through a central gateway across a plurality of functional modules; with access control to each functional stake holder; and transmitting the data, for access to sponsors over the network.

Abstract: The disclosure is directed to a process and system for managing the end-to-end process of obtaining research data from patients and/or participants in a Clinical Trial. The process enables collection of appropriate informed consent from patient/participants via electronic devices such as smart phones and tablets. Additionally, the system uses biometric information such as finger prints, face pictures, digital signature to provide additional information concerning a participant. This helps to make the whole informed consent process effortless, paperless and transparent. An aspect of the disclosure enables investigators to reach out to a wider patient/participant population irrespective of their physical location. Thus the platform enables investigators to collect and transfer real time data, seamlessly from across the world.