BIONOTE

Downloadable computer software for capturing, reporting, and processing of data in pharmaceutical industry clinical trials; recorded computer software for the collection, editing, organizing, modifying, book marking, transmission, storage and sharing of patient-reported outcomes in pharmaceutical industry clinical trials; recorded computer software for the collection, editing, organizing, modifying, book marking, transmission, storage and sharing of patient-reported outcomes in pharmaceutical industry clinical trials on handhelds and PDAs; downloadable computer software for the collection, editing, organizing, modifying, book marking, transmission, storage and sharing of patient-reported outcomes in pharmaceutical industry clinical trials; downloadable computer software for the collection, editing, organizing, modifying, book marking, transmission, storage and sharing of patient-reported outcomes in pharmaceutical industry clinical trials on handhelds and PDAs; downloadable mobile applications for generating patient-reported outcome reports in pharmaceutical industry clinical trials; downloadable software for enabling patients to select a medication from a list of their frequent medications, select a new drug or therapy, and enter all medication intake, and for adding the aforementioned information to existing study questionnaires as a way to record concomitant medications; Downloadable computer software and downloadable mobile application software for use in clinical trials and clinical research for the collection, capture, processing, transmission, storage, synchronization, reporting, and management of electronic clinical outcome assessment (eCOA) data, patient-reported outcomes (ePRO), electronic diaries (eDiary), electronic clinician-reported outcomes (eClinRO), electronic observer-reported outcomes (ObsRO), and performance outcome assessments (PerfO); downloadable computer software and downloadable mobile application software featuring reminders, alerts, notifications, training materials, administration of assessments and questionnaires, compliance monitoring, real-time reporting, offline data capture, and data synchronization for use in pharmaceutical, biotechnology, medical device, and clinical research studies

Software as a service (SaaS) services featuring software for use in clinical trials and clinical research for the collection, capture, processing, transmission, storage, synchronization, reporting, and management of electronic clinical outcome assessment (eCOA) data, patient-reported outcomes (ePRO), electronic diaries (eDiary), electronic clinician-reported outcomes (eClinRO), electronic observer-reported outcomes (ObsRO), and performance outcome assessments (PerfO); providing temporary use of non-downloadable software featuring reminders, alerts, notifications, training materials, administration of assessments and questionnaires, compliance monitoring, real-time reporting, offline data capture, and data synchronization for use in pharmaceutical, biotechnology, medical device, and clinical research studies; Biomedical, pharmaceutical, biotechnology and health-related research study services, namely, conducting clinical trials in the field of clinical trials of drugs, medical devices and other interventions to determine efficacy and safety, particularly, providing the selection of trial subjects in accordance with research design criteria, trial management and site monitoring, monitoring trial participants for adverse reactions and preparation and presentation of reports of adverse reactions, administration of clinical trial data and safety monitoring boards, collection and management of study data, clinical data management services and medical coding, analysis of study data including selection and application of statistical tests to study data, providing biostatistics and statistical programming, dispensing drugs and managing drug inventories, monitoring design and conduct of trials for compliance with applicable regulations and policies and preparation and presentation of compliance reports, development and maintenance of internet websites for reporting on studies, medical writing and graphic design of research study protocols, preparation of reports of research studies and abstracts of reports, preparation and presentation of reports to study sponsors and regulatory authorities.