— Good Clinical Practices (GCP) - Society for Clinical Research Sites – SCRS
Good Clinical Practices (GCP)

Webinar Series/Good Clinical Practices (GCP)

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As of May 2018, the EU General Data Protection Regulation applies to clinical trial data generated in the EU. What is the consequence of this EU regulation? How does it affect our trials?Continue reading…

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Life sciences companies must cater to two conflicting agendas when it comes to clinical data management. First, they must manage the requirements of clinical trials and share the results rapidly. Second, they have to ensure that all the patients’ results align with their long-term personal medical records.Continue reading…

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Although the high-level processes of risk-based monitoring are aligned, practical implementation often differs from company to company. This might cause confusion around what sites can expect from RBM practices and create a lack of clarity around how sites will benefit. Join this webinar to gain a deeper understanding of the expectations, process and impact of risk-based monitoring for sites.Continue reading…