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Avoid Enrollment Pitfalls: Find Your Best-fit Clinical Trial Sites
Six Practices of High Performing Clinical Research Sites
Learn what high-performing research sites have in common, and what makes sponsors return to them again and again.
Rare & Orphan Disease Endpoints: Challenges & Examples from Neurodevelopment
Subject Recruitment Materials: Understanding the Requirements for IRB Review
Recruiting Patients & Time Management: Top Tips for Dealing with the Most Critical Resource in Research
Personalized Medicine Requires Personalized Measurement
Rare Disease Case Study: Familial Amyloidosis
Our client, a top-tier CRO, was faced with the challenge of enrolling for a non-interventional screening study in the familial amyloidotic cardiomyopathy (FAC) patient population.
Looking Ahead to 2018: Insights into Clinical Research Trends from Our Experts
In this paper, WCG thought-leaders provide insights on what they anticipate in 2018 in clinical trial technology, regulatory changes, and scientific developments.
Solving The Problem of Clinical Research Enrollment
Strategies that Inform Investigator Selection and Enhance Enrollment
Investigational Drugs Outside of Clinical Trials - Understanding Expanded Access and Right-to-Try
Case Study: Addressing Placebo Response
Understanding the Challenges of Managing Combination Product Safety Reporting
Harnessing the Power of Data to Optimize Site Selection for Clinical Trials
Managing the Unmanageable: Meeting the Challenge of Appropriate Safety Report Distribution
Infectious Disease Challenge Studies: Ethical Issues in Causing Disease for Medical Knowledge
Early Access to Investigational Drugs: Lessons Learned from Ebola
Learn about the regulatory framework that governs the use of investigational drugs outside clinical trials (formerly called “compassionate use”), and the ethical challenges surrounding it.
Rare Disease Case Study: Pediatric Sickle Cell Anemia
Our client, a Top 10 pharmaceutical company, needed to boost enrollment for their phase ll pediatric sickle cell anemia study.
Reducing Study Team and Site Burden through an Integrated eClinical Platform Solution
Towards Total Quality Management in Human Research Protection Programs: IRB Administrative and Reviewer Activities