The clinical trials landscape continues to evolve and with it, an exponential growth in the adoption of electronic informed consent (eConsent) solutions. These solutions deliver a myriad of benefits for trial sponsors, sites and patients. However, there is still some reluctance to adopt these solutions due to perceived costs associated with implementation and training.
The Importance of eConsent
Clinical trials are evolving with novel designs, hybrid and decentralized protocols and an increased focus on diversity, equity and inclusion. An adaptive eConsent platform supports these diverse trials, reaching patients globally while also tailoring information to individual needs, including age, culture and learning styles.
