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The Future: How We Can Reach the “Brave New World” of Diverse and Equitable Clinical Trials, Upcoming Webinar Hosted by Xtalks
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This is the fourth webinar in a four-part series from Syneos Health® titled “Blazing a Trail to Clinical Trial Diversity”. In this free webinar, attendees will learn about potential regulatory changes that could be made to increase greater patient diversity in clinical trials and understand the benefits of inclusive trials. The featured speakers will also discuss how to reward organizations for creating truly equitable clinical trials.
The presenters explore how or if policy innovations, such as regulatory mandates and incentives, can move the industry forward as one.
An ISO 14155:2020 Primer â Good Clinical Practice For Medical Device Trials
By Sandra SAM Sather and Jennifer Lawyer, Clinical Pathways, LLC
The International Organization for Standardization (ISO) recently released
ISO 14155:2020, Clinical investigation of medical devices for human subjects Good clinical practice,
1 a standard developed to guide clinical research professionals during the design, conduct, recording, and reporting of clinical trials related to the safety and effectiveness of medical devices. For post-market clinical trials, it should be followed as much as it is relevant to the particular clinical trial or according to regional requirements. The standard outlines requirements to:
Protect of the rights, safety, and well-being of human subjects,