Optimizing a Clinical Development Program to Improve ROI
Clinical development proceeds in phases, and each phase contains a set of clinical trials. These trials, including their sample size […]
Clinical development proceeds in phases, and each phase contains a set of clinical trials. These trials, including their sample size […]
A well-utilized CTMS streamlines financial workflows, automates participant payments, tracks budgets, and centralizes data, helping clinical sites maximize ROI and efficiency.
The past year has been one of the most challenging ever for those working in healthcare and clinical research. The
A key element to successful study startup is identifying efficiencies to help meet critical milestones. Engaging with research compliance experts
Staff Augmentation aids data migration by assessing workflows, ensuring a smooth transition to OnCore, and empowering teams with tailored training.
Compliant document storage in clinical trials demands robust systems for security, accessibility, and retention to meet privacy and regulatory standards.
The data gathered in a clinical trial is often collected by many different people, including investigators and coordinators, and interpreted
Questions still remain about GDPR and its applications. Have you considered these six key questions to ask within your organization?
The European Union’s General Data Protection Regulation (GDPR) goes into effect May 25, 2018, replacing the existing EU Data Protection
Learn the necessary steps to create an effective SOP for data collection in clinical trials.
This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.