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  • Flipping the Funnel in Patient Recruitment to Accelerate Enrollment Timelines31:28

    Flipping the Funnel in Patient Recruitment to Accelerate Enrollment Timelines

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  • Something Has to Give: The Current Unsustainable Approach to Safety Reporting Puts Trials and Patients at Risk

    Something Has to Give: The Current Unsustainable Approach to Safety Reporting Puts Trials and Patients at Risk

    Something Has to Give: The Current Unsustainable Approach to Safety Reporting Puts Trials and Patients at Risk

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  • Quality First: Using Data to Inform Site Selection in CNS

    Quality First: Using Data to Inform Site Selection in CNS

    WCG MedAvante-ProPhase espouses a rather simple philosophy: minimize variability, generate cleaner data.

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  • Reinventing Site Feasibility: Moving from Simple Survey to Relationship Management32:54

    Reinventing Site Feasibility: Moving from Simple Survey to Relationship Management

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  • Clinical Trials in the Era of Precision Medicine44:43

    Clinical Trials in the Era of Precision Medicine

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  • Site Score Card: Expert Tips for Moving Up the Ranks

    Site Score Card: Expert Tips for Moving Up the Ranks

    How can a site move up the selection list and participate in these trials? It’s as simple as one word: metrics.

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  • Six Practices of High Performing Clinical Research 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.

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  • From the "Ask the IRB Experts" blog

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  • Not Like Everyone Else: Unique Challenges for Small & Emerging Biopharma Companies

    Not Like Everyone Else: Unique Challenges for Small & Emerging Biopharma Companies

    Small and emerging biopharmas are conducting almost 50% of clinical trials in the U.S., often with lean teams, resources and infrastructure. Learn how to reduce the pressure on teams and timelines.

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  • Question: What are the requirements for submitting protocol deviations?

    Question: What are the requirements for submitting protocol deviations?

    Some deviations from the IRB approved protocol are planned while others are unintentional or unplanned. The FDA and HHS (45 CFR §46.103(b)(4) and 21 CFR §56.108(a)(4)), position is that...

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  • Question: Does the IRB need to review news stories?

    Question: Does the IRB need to review news stories?

    The local newspaper is planning to run a story on a new clinical trial that will highlight the development of an exciting new drug and the work done by our principal investigator...

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  • New Blog: "Ask the IRB Experts"

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  • Recent Videos

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  • Question: When can research participants be paid?

    Question: When can research participants be paid?

    As a sponsor, what do the regulations say about paying research subjects? What are acceptable practices for compensating subjects for participating in a clinical trial?

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  • The Role of Expert Committees: An interview with Dr. Seltzer13:58

    The Role of Expert Committees: An interview with Dr. Seltzer

    What’s the role of expert committees today? What’s happening on the regulatory side? Dr. Seltzer, Chief Scientific Officer of WCG Clinical, shared his insights on expert committees during a recent...

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  • Eliminating the Headache of Global Safety Reporting to Investigators and Ethics Committees32:32

    Eliminating the Headache of Global Safety Reporting to Investigators and Ethics Committees

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  • Portfolio Based Data-Driven Site Selection30:39

    Portfolio Based Data-Driven Site Selection

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  • Case Studies

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  • Recruiting Patients & Time Management: Top Tips for Dealing with the Most Critical Resource in Research52:22

    Recruiting 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.

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  • How Roche Optimized its Global Safety Reporting Process for Clinical Trials

    How Roche Optimized its Global Safety Reporting Process for Clinical Trials

    Roche recognized several major challenges that its CTSP 2.0 system needed to address.

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  • By the Numbers: Six Challenges to Enrollment, One Customized Solution

    By the Numbers: Six Challenges to Enrollment, One Customized Solution

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  • OhioHealth Case Study

    OhioHealth Case Study

    Dissatisfied with its electronic IRB research management solution, OhioHealth Research & Innovation Institute searched for a solution to improve compliance, efficiency, customer service, and cost.

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  • Whitepapers

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  • How a Sponsor Secured 200 High-Performing PI's in a New TA in Just 5 Days

    How a Sponsor Secured 200 High-Performing PI's in a New TA in Just 5 Days

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