01
Notifications: to remind you of their appointments and inform them if other clinical studies are available near them.
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Mobile/tablet friendly
web application.
Clinical trials are a fundamental part of medical research that aims to find new ways to prevent, detect or treat diseases. These new treatments can be new molecules, combinations of different molecules, new ways of administering them, new treatment techniques (surgery, radiotherapy). The goal of clinical trials is to improve the treatment of patients at all stages of the disease. They allow us to evaluate the effectiveness and tolerance of new treatments before they are put on the market. When you participate in clinical research, you help doctors and researchers learn more about diseases and find alternative treatments for your disease.
As an IBD patient, you have probably done a lot of research about your disease and its different stages, you have explored several websites and forums in search of answers, support or simply to exchange information. Telemedicine Technologies puts at your disposal the afa website that you can consult through the following link. afa is the only French association that supports and informs Crohn’s and ulcerative colitis patients and their relatives, defends their rights, and finances research.
Access ToTem4meWe understand the difficulties you are going through and the obstacles you face in finding clinical trials that are right for you. At Telemedicine Technologies, we support you and are actively working with physicians and patients (through the afa) to provide you with easy access to clinical trials near you so that you can find the innovative treatments you want and deserve. in a few clicks and minutes wherever you are! in total security!
Access ToTem4meOn-line Patient Questionnaire
Connect to the ToTem4me application, fill out a questionnaire in 2 minutes, and find out if there are ongoing clinical trials in your area of choice that could potentially suit you.
Coordinator interview & study identification
The expert coordinator finetunes with you the identification of potential study(ies), explains clinical studies typical process, and confirms your interest.
Site
referral
The expert coordinator forwards your contact details to the hospital you select, so that an appointment is given to you. The investigational team confirms your potential eligibility and initiate the screening.
Patient
follow-up
The expert coordinator follows-up with the investigational team to ascertain that you had your appointment and enquires on the follow-up proposed.
Your data is never shared with a trial site You have the right to be forgotten and have your data fully deleted. the coordinator has no access to your personnal datas Only limited information is captured to protect your privacy ToTem4me is GDPR compliant
January 30, 2025
MedtechDive Artificial intelligence was a topic of focus for the medical device industry in 2024. Companies including GE Healthcare, Medtronic and Dexcom touted new AI features, and others like Stryker and Quest Diagnostics added AI assets through M&A. Meanwhile, conversations about regulations and generative AI, models that are trained to create new data including images and text, dominated medtech conferences. The Food and Drug Administration recently […]
January 30, 2025
BioPharm International FDA published a final guidance on Jan. 2, 2025 for those interested in participating in the agency’s Advanced Manufacturing Technologies Designation Program, which was developed to facilitate drugs manufactured using advanced manufacturing technologies (AMTs). The guidance, Advanced Manufacturing Technologies Designation Program, is the final version of the draft document issued on Dec. 13, 2023. […]
January 30, 2025
Applied Clinical Trials Online Medable has shared new data from the Tufts Center for the Study of Drug Development (CSDD)’s PACT Consortium linking decentralized clinical trial (DCT) approaches to a higher rate in participation across multiple demographic groups. The new research shows that a more strategic implementation of DCT elements, combined with increased regulatory oversight, […]