
Total Consent offering is an SaaS electronic consent management solution compatible with clinical trials in over 120 locales worldwide.
Total Consent offering is an SaaS electronic consent management solution compatible with clinical trials in over 120 locales worldwide.
Combines Haselmeier´s D-Flex™ Logbook with AARDEX Group’s Medication Adherence software and hardware ecosystem.
Ten-year partnership will help Merck reduce operational costs and deliver value to patients, HCPs.
Deeper focus on patient engagement across the pharma/biotech product lifecycle.
Richard Williams, PhD, chief medical officer at Kinnate Biopharma Inc. discusses clinical trial strategies and challenges.
Suite includes DCT applications, an eCOA oncology library, and protocol design consulting.
Company exceeds enrollment goal for its AI platform.
Collaboration in EDC renewed for another five years.
Partnership will enable over 150 sites in 22 states to accept patients for respiratory clinical trials involving precision imaging.
Services include data support in drug submissions and oncology.
IRT system enhanced with new self-service functionality.
New clinical data application utilizes study data from multiple sources to provide accurate clinical trial data.
Collaboration to promote drug and diagnostics R&D in the fields of metabolic disease and autoimmune neurology.
The latest business and people happenings of the past month, all in one place.
Pursuing new tools and capabilities in sample logistics, storage, and data analysis.
Approaches sponsors, CROs, and investigators can take from the DMD experience.
As activity in this space grows, so do the hurdles in moving these products forward.
Chamber of Commerce for Greater Philadelphia ranks city No. 2 overall for cell CGT hubs.
Veeva Link SiteBase and Veeva Link TrialBase to identify sites and optimize trial design.
Module to address need for increased study access and engagement.
Collaborative initiative will publish a publicly available methodology for calculating and comparing the footprint of centralized and decentralized clinical trials.
Partnership will aid cancer patients in finding appropriate clinical trials.
Recruiting sites drop 48% in Ukraine and 52% in Russia, yet more than 2,500 trials still running in region.
Ro's telehealth platform will be used to remotely screen and recruit patients eligible for NIA dementia trials.
New offering combines laboratory services, patient-focused logistics, and self-collection technology.
EMR/EHR patient identification technology will be integrated into RealTime's CTMS.
Integration with Curavit's DCT platform aims to speed trial enrollment and improve retention.
Study aims to better understand how to reduce delays in diagnosis, decrease disparities in care, and improve outcomes in patients with Alpha-1 Antitrypsin Deficiency.
New operational guide highlights handling safety reporting to investigators, ethics committees, and competent authorities.