Objective To assess whether post-authorisation studies registered with the European Medicines Agency (EMA) adhere to legislation and recommendations to publicly post study protocols and results.
Company to host investor webcast and conference call on February 12 at 7 a.m. PT / 10 a.m. ET Investor webcast will feature the clinical validation data and review commercial launch timeline BRISBANE, ...
Margaret Lozovatsky, MD, FAMIA, has spent years helping health systems adopt digital tools designed to improve patient care. As a pediatric hospitalist, she has also seen what can go wrong. In one ...
The current US system of reimbursement for dementia care does not support the complex biospychosocial needs of families living with Alzheimer disease and related dementias. We propose an alternative ...
Ameve Sharma spotted a dearth of modern, science-backed ayurvedic brands, and went on to build Kapiva to fill this gap Kapiva generates about 35% of its revenue from its own website, 40% from online ...
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