Patient Engagement
-
Read Flipbook
Case Study - Top 5 Pharma Enrolls 56% Faster with WCG Site Augmentation
-
Read Flipbook
Case Study - Top 5 Sponsor Enrolls 30,000+ Patients in Just Over 3 Months With WCG Site Augmentation
-
Benchmark your study enrollment versus competitors
Get Benchmark Data -
Read Flipbook
Invert to Convert: Rethinking Patient Recruitment and Enrollment Strategies
-
Read Flipbook
Solving the Problem of Clinical Research Enrollment
-
Read FlipbookWCG ThreeWire - Chart Review
-
52:22Watch VideoRecruiting Patients & Time Management: Top Tips for Dealing with the Most Critical Resource in Research
Learn how to engage sites more effectively with the appropriate recruitment resources, use dedicated staff to manage recruitment efforts, and eliminate bottlenecks and expedite recruitment timelines.
-
Read PostInfograph: Rethinking Patient Recruitment
Despite advances in science, medicine and tech, 90% of clinical trials struggle to meet enrollment. We propose flipping the funnel to address site resourcing issue and convert recruits into enrollees.
-
Read FlipbookSite Based Enrollment Programs at a Global Scale
-
Read Flipbook
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.
-
Read FlipbookQ&A with CNS Expert, Dr. Leslie Citrome
Leslie Citrome, MD, MPH, a member of WCG’s Scientific Leadership Team, shared his insights during a recent conversation with Mark Opler, MD, PhD, chief research officer at WCG-MedAvante-ProPhase.
-
Read FlipbookQ&A with CNS Expert, Dr. Christoph U. Correll
Christoph U. Correll, MD, a member of WCG’s Scientific Leadership Team, shared his thoughts in a recent conversation with Mark Opler, MD, PhD, chief research officer at WCG-MedAvante-ProPhase.
-
Read FlipbookTrend: Genetic Testing and Data Privacy Ownership
-
Read Flipbook
Clinical Trial Recruitment Practices: The Evolution of Ethical Considerations
-
Read Flipbook
Subject Recruitment Materials: Understanding the Requirements for IRB Review
Often, the only way for potential research subjects to learn about a clinical trial is through recruitment materials. But what materials must you submit to the IRB for review?
-
Read FlipbookeCOA: Keep it Simple, Exec Argues
Nearly half of all clinical trials still use paper as the primary - or even sole - source of records while barely a quarter of trials use eCOA or ePRO
-
Read FlipbookCNS Drugs Take Longer to Develop, Win Approval
CNS drugs take 20% longer to develop and about 19 months (36%) longer on average than other meds to win FDA approval after clinical trials
-
Read Flipbook
Clinical Trials and Social Media - Friends or Foes?
-
Read Flipbook
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.
-
56:41Watch VideoRare & Orphan Disease Endpoints: Challenges & Examples from Neurodevelopment
-
Read FlipbookPersonalized Medicine Requires Personalized Measurement
How we measure outcomes will evolve from applying one solution to finding an empirical basis for a highly customized application of all of them, enabled by technology
-
Loading More...
