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WCG’s Unmatched Experience in Early Phase Hematology and Oncology

WCG Clinical

Unmatched Experience in Early Phase Hematology and Oncology Discover unparalleled expertise in phase I hematology and oncology study reviews with WCG. As the foremost leader in ethical and scientific review services for oncology studies in the US, we have successfully conducted over 3,300 early phase oncology study reviews.

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WCG Raises the Bar in Quality Management Standards, Becoming ISO 9001 Certified in both IRB and IBC

WCG Clinical

PRINCETON, NJ, October 10, 2023: WCG, the global leader in providing solutions that measurably improve and accelerate clinical research, announced today the extension of its ISO 9001 certification to its Institutional Biosafety Committee (IBC) services by BSI. For more information, visit [link].

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WCG Revolutionizes Ethical Review Process with IRB+ Service, Achieving Unprecedented Efficiency Gains

WCG Clinical

PRINCETON, NJ, November 30, 2023 – WCG, the global leader in providing solutions that measurably improve and accelerate clinical research, announced today the official launch of IRB+, a groundbreaking service that transforms the landscape of Institutional Review Board (IRB) operations.

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?5 Things You Need to Know from Our Recent Gene Therapy Webinar

Worldwide Clinical Trials

Fewer staff creates many problems, including less bandwidth to meet for reviews and approvals. Patients often don’t have time to wait for delays to resolve, so if the Institutional Review Board (IRB) is unable to meet to approve their participation, then patients may have to move on to seek other more available treatments.

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Clean Bench vs Biosafety Cabinet: What’s the Difference?

Advarra

Institutional biosafety committees (IBCs) frequently receive questions about the proper type of hood for use with biological materials and the difference between biosafety cabinets versus clean benches. Why Does the IBC Prefer Researchers use a Biosafety Cabinet vs a Clean Bench?

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A Checklist for Optimizing Clinical Trial Study Startup Activities

Advarra

Securing oversight committee approvals (IRB, IBC, SRC, RSC, COI, feasibility) . Scheduling this conversation upfront with an IRB will save both the sponsor and IRB time during review time. . Need additional guidance on review requirements? . What Level of Review Does Your Study Need? . FDA-USA, BfArM-Germany) .

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Patient Retention Insights: Use Payments to Enrich Diversity, DCTs Need Special Attention

ACRP blog

A key focus in the clinical trial diversity plans that are part of this year’s omnibus spending bill signed by President Biden should be participant payments and reimbursement, writes Kelly FitzGerald, PhD, IRB Executive Chair and Vice President for IBC Affairs at WCG IRB. There are no simple solutions.