The global clinical trials market is expected to grow by almost 7% a year for the next 10 years. How can the Allyfe platform sustain that growth and differentiate it self from the competition?
Continue ReadingConsent is a major phase of the trial enrollment process, submitted to strict legal constraints. Additionally, it is stilloften paper-based, which makes it logistically complex. Reconsents might even be more problematic....
Continue ReadingScalability, flexibility and a pragmatic risk-based approach make the Allyfe platform compliant in a unique way. Every part, every module of the platform incorporates data security and privacy demands by design.
Continue ReadingThe dashboard is a powerful trial optimization tool. It saves time, allows benchmarking and favors reactivity. it turns patients into actors of the enrolment procedure!
Continue ReadingA flexible and extensive scheduling tool can save time, reduce no shows, but also improve patient engagement and even facilitate compliance
Continue ReadingUserfriendly and secure communication channels between sponsors and investigators, and between investigators and patients, enhance patient engagement and improve trial efficiency.
Continue ReadingEquality, diversity and inclusion can boost life sciences and help clinical trials move forward.
Continue ReadingThis article is based on a recent study carried out in Denmark. It scientifically analyzes that low dropout rate in a virtual clinical study of atopic dermatitis is achieved through weekly reward-based personalized genetic lifestyle reports.
Continue ReadingI find it wonderful that when a ML software detects a tumor, a radiologist has to confirm it before any action can be taken. Human intervention always comes first. It is also a way to acknowledge that AI applications have been elaborated by human beings, and thus are never flawless.
Continue ReadingThe use of technology drives the number o fclinical trials needed to apply these technologies through the roof. And yet,ironically enough, it seems very difficult to resort to technologies to make all these necessary clinical trials cheaper or faster.
Continue ReadingAlthough a trial can be stopped for many reasons, problems with patient recruitment and retention are often cited as reasons why trials have been halted.Studies on the reasons for this dropout phenomenon simultaneously strengthen the need for regular interactions between doctor/researcher and patient as a way to defuse doubts and discouragement, and paradoxically reveal new potential for AI (Artificial Intelligence) interventions into patient recruitment.
Continue ReadingAs obvious as it may seem, our national motto is the main inspiration behind Allyfe joining Biowin, Wallonia’s health cluster, or, as they state: the gateway to health biotechnology and medical technology excellence in Wallonia and beyond!
Continue ReadingThis is the kind of slightly provocative (and thus catchy !) titles which has appeared more and more often in the media and on the internet in the last weeks and months. In most cases it was a celebration of human resilience in the face of adversity. Also the sign that the worst was behind us since we could allow ourselves to look for the silver lining.
Continue ReadingAntimo, you are the CEO and Founder of Allyfe. Since you have been active in the field of clinical trials for quite a while, you must be familiar with the recurrent issue of patient recruitment ?
Continue ReadingThe Covid-19 pandemic has catalyzed the adoption of decentralized clinical trials. The increase in trial activities conducted remotely and in participants’ home has been tremendous. The conclusion is obvious: the future trial paradigm is meeting patients where they are.
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