Gino DiSciullo, CEO ClinOne plans out an entire trial from scratch with advanced tasks and checkpoints involved. The eClinical tool manages the on-site contacts and the various teams going through a clinical trial. Scheduling trials for a client and monitoring the patients during a trial is an area of expertise for ClinOne. The solution is also responsible for enabling the setup, collection, storage, tracking and archiving of the essential clinical study documents.
The mobile app solutions offered by ClinOne are ClinOne trial awareness and ClinOne eConsent which are focused to deliver clinical trial content to the participants. The ClinOne information platform aims to improve the engagement between academic researchers, drug developers and patients to help and advance clinical trials.
ClinOne’s trial awareness app works by sending automated eNewsletters with listings of currently active studies on behalf of the research teams to the patients. Health care providers also have access to the ongoing studies through the web site and the mobile applications.
ClinOne eConsent app enables patients to access the actively available processes. Patients can choose from on-site visits, complete remote services or an option bridging the two, based on their needs. The solution is designed to transfer data with other eClinical systems used across the globe and is easily configurable making it affordable and quickly customizable.
A Patient’s compliance for timely visits is important for the overall success of the clinical trials.
Transportation has often been cited as a barrier to clinical trial participation and over 3.6 million delays and misses are recorded each year in non-emergency medical care due to transportation.
ClinOne offers a true single platform CTMS solution enabled with explainer videos and knowledge checks, accessible by up to 10 patients at once to create a community over a digital platform. The incorporation of the eTrial master file strategy enables the app to setup, store, track and archive the essential study documents.
The mobile application interface is programmed with web hooks that send automated messages to the patients with updates regarding the dosages, number and timings of the medications. Easy user-interface can be used to join the mobile access when working in the remote mode and the integration of the enterprise eConsent strategy simplifies and reduces administrative burdens, ensuring compliance for sites and study teams.
The solutions are available with updated ICF document version so the study participants are well aware of their rights, purpose and duration of study, required procedures and key contacts.
ClinOne eConsent audits and evidences the sequence of activities at any time during a specific operation, and allows users to sync data from connected devices to sync data. The easy real-time dashboard on the app tracks consent progress for all the patients across the trial and helps advance the drug and medical device clinical trials.
To all our customers, in a time of change and uncertainty, I am fully committed to building upon an already strong foundation to ensure ClinOne is the technology partner you trust and value most
With easy engagement between academic researchers and patients, access to solutions from the mobile application, and transportation to and fro the clinics for study visits, ClineOne has further simplified the industry's standards, adding to its already esteemed reputation. ClinOne now stands as a bench mark for simplified and assisted solutions in the clinical trial industry, by providing simplified solutions with added amenities, and introduce new strategies to cope with challenges to come.
