Education

Overseeing and Operationalizing Patient Recruitment Across Study Stakeholders

This webinar will tackle the most pressing challenge in clinical research: achieving enrollment targets on time. Our presenters will investigate the recruitment lifecycle across key stages, including vendor referrals, prescreening, consent, and more. Additionally, they will examine how sponsor and CRO study teams can gain better insight into recruitment activities and to predict, analyze, and intervene appropriately.

IRB featured image, including photos of clinical research professionals collaborating in an office

Revised Common Rule Reference Guide

The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for multisite and minimal-risk research.

Site technology reviews featured image, including clinical research professionals working with patients and collaborating

Clinical Data Management 

SITE TECHNOLOGY Clinical Data Management  Streamline Your Data Collection and Management Standardize your clinical data practices to accelerate collection, ensure

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