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Most Recent Flipbooks
Written Procedures for IRBs: What Does the New Final Guidance from FDA and OHRP Mean to You?
Five Essential Considerations for Efficient Site Contracts and Payments
Innovation in Investigator Site Contracting
Clinical Study Sites Struggle to Manage Responses to Ad Campaigns
Shifting the Tide of Inefficient Site Contract Negotiations: Turn to an Expert
Best Practices: Integration of IRB and IBC Review
Avoid Enrollment Pitfalls: Find Your Best-fit Clinical Trial Sites
Selecting the right site is the single most crucial decision you’ll make about your next clinical trial. And perhaps the single most important consideration in selecting a site is whether it can make
Not Like Everyone Else: Unique Challenges for Small Biopharma Companies
Solving the Problem of Clinical Research Enrollment
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.
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.
Is It Gene Therapy? Debating a Controversial Definition
Pragmatic Clinical Trials: What You Need to Know
Clinical Trial Recruitment Practices: The Evolution of Ethical Considerations
Gene Therapy & Immunotherapy Glossary, 2nd Edition
The Second Edition of WCG’s wildly popular Alphabetical Glossary of Terms in Gene Therapy and Immunotherapy.
Choosing the Right Solution: Improving the Site Feasibility Process
Investigational Drugs Outside of Clinical Trials - Understanding Expanded Access and Right-to-Try
Managing the Unmanageable: Meeting the Challenge of Appropriate Safety Report Distribution
Addressing the Challenges of Human Tissues and Cell Products Regulation
Subject Recruitment Materials: Understanding the Requirements for IRB Review