Science 37 Introduces Native Support for Apple and Android
Science 37 has created a patient experience while introducing native support for iOS and Android operating systems. With this development, patients can not only participate from the comfort of their own home, but they can also do it with the familiarity of their own smartphones.
Using their own devices (BYOD), patients can learn more about a study, provide consent, schedule and participate in study visits, complete assessments, and communicate directly with the Science 37 study team and investigators, all through a single platform.
The intuitive, cloud-based platform also integrates workflow and processes for physician investigators, mobile nurses, and coordinators across the entire trial life cycle. Combining these advantages with native support for iOS and Android further enhances the company’s ability to deploy its services globally.
Chris Ceppi, chief product officer of Science 37 says, “The fully integrated mobile capabilities we’re introducing enable a patient experience that sets a new standard for clinical studies.”
In addition to the platform, Science 37 has also conducted more fully decentralized, interventional clinical trials-all the way from protocol design to database lock. Coupled with its telemedicine and home health network, Science 37 enables coverage around the world.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
FDA Grants Ziftomenib with Breakthrough Therapy Designation for NPM1-Mutant Acute Myeloid Leukemia
April 23rd 2024Data from the Phase Ib portion of the KOMET-001 trial showed that the once-daily oral treatment may provide a substantial improvement over available therapies for relapsed/refractory NPM1-mutant acute myeloid leukemia.
