Set up the legal requirements to accelerate your trial.
Implement patient engagement plans to increase retention.
We provide expert resources to evaluate your firm’s privacy preparadeness and to develop procedures and policies to handle GDPR requirements. This will accelerate the start-up of your clinical trials in Europe.
Our experts can provide the following services:
Patient dropout is a costly problem for clinical trial sponsors, who have consequently focused their attention on patient retention factors and on its corollary, patient engagement. It is widely believed that patients’ early and continued involvement throughout a study can indeed prevent dropout and lead to faster time to market at lower costs. To respond to that patient retention need, Allyfe can devise a specific engagement plan for your clinical trial.
What does the plan encompass?