DPharm 2023 has come to a close, and as we reflect on the sessions and insights shared, two themes clearly stood out this year: The participant experience and i...
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In the fast-paced world of medical research, patient advocacy groups have emerged as powerful drivers of change. One critical ingredient in their recipe for suc...
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Precision medicine trials introduce requirements that most traditional recruitment and enrollment workflows are not designed to handle. Genetic eligibility, bio...
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Last month, our team had the pleasure of attending the European Network to Cure ALS (ENCALS) meeting, an annual gathering that brings together some of the brigh...
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£330K grant awarded to support and engage patients at risk of MND/ALS, and track the psychological impact of genetic testing.
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This webinar, featuring Sano Genetics team members Ross Rounsevell and George Bowley, highlights the importance of purposeful participant engagement in research...
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Patient centricity has become increasingly important in clinical trials for ALS. In this webinar, host Paul Wicks and Cathy Collet discuss the challenges of pat...
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Clinical trials depend on sustained patient participation, yet recruitment shortfalls and early withdrawals remain two of the most common causes of trial delays...
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Electronic consent, or e-consent, is a method of obtaining informed consent through an electronic system rather than a paper form. It typically incorporates mul...
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This webinar, hosted by Sano Genetics Partnership Lead Lindsey Wahlstrom-Edwards and featuring representatives from COUCH Health, Lupus Research Alliance, and A...
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