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Most discussions around patient involvement in clinical trial design focus narrowly on the participant...
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ICH E6(R3) requires sponsors to perform risk-based, timely, and focused audit trail reviews as part...
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Accelerating Innovation in Structural Heart Care: Bioforum’s Role in Pi-Cardia’s FDA Journey Bioforum is proud...
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Introduction With over 50%[1] of drugs in development reflecting rare/orphan and oncology indications alone, the...
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Selecting the right Contract Research Organization (CRO) partner is a critical decision for any pharmaceutical,...
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In today’s evolving clinical research and drug development landscape, with more data sources and technology...
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Timing is critical in clinical trials, especially when it comes to risk assessment. Earlier risk...
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Ensuring Clinical Trial Data Integrity: Five Things to Remember When Selecting a CRO Partner ...
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The International Conference on Harmonization Good Clinical Practice (ICH-GCP) defines the Sponsor of a clinical...
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