MedPoint Digital Expands Mobile Services for Clinical Trials
MedPoint Digital, a digital services provider to the global biopharma industry, recently announced a new generation of eClinical technologies for mobile devices. The new mobile-friendly platforms deployed by MedPoint include:
- TriPort Clinical Trial Portal—MedPoint has evolved its core clinical portal to span the worlds of desktop and mobile, so it is compatible across devices, operating systems and browsers. TriPort is a secure, fully validated clinical trial technology that delivers study-specific information, training, and communications. TriPort is built for interoperability and supports role-based access to study resources and individual tracking of activity completion.
- TelePoint Virtual Meeting System—The latest TelePoint release is cross-platform compatible, supporting live virtual meetings that simultaneously connect participants from desktop computers, smart phones, and tablets. This proprietary system works across all major operating systems and devices, blurring the lines between conventional web conferencing and app-enabled conferencing.
- ActivMedia Modules—MedPoint has implemented a new mobile-compatible development platform to produce its next generation of multimedia/interactive web modules. Using its ActivMedia platform, MedPoint develops intuitive web modules that engage users for self-learning, real-world simulations, and training certification.
- SFX Site Feasibility Xelerator—With the latest release of the SFX platform, study sites can complete survey forms over their mobile devices, making it faster and easier for sponsors to collect site profile information into a secure workspace for analysis, vetting, and promotion.
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.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.
