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One of the key challenges in #DMD research is ensuring the availability of high-quality biospecimens for analysis. As DMD is a #raredisease, obtaining an adequate number of samples can be difficult. Furthermore, the diversity of the patient population must be considered to ensure that research findings are applicable across different ethnicities and genetic backgrounds. Historically, clinical trials and research studies have primarily included individuals of caucasian descent, leading to a lack of representation from other populations. However, recent efforts have been made to address this disparity and promote #diversityinDMD research. Initiatives such as the #DMDHumanTissueBank, established by Cooperative International Neuromuscular Research Group, aim to collect and distribute biospecimens from individuals of diverse backgrounds. Garner Bio stands at the forefront of supporting pre-clinical research into Duchenne Muscular Dystrophy (DMD) by providing a diverse array of biospecimens sourced with utmost adherence to rigorous U.S. standards and protocols, including 45 CFR part 46, HIPAA, 21 CFR Part 50/56, and the Uniform Anatomical Gift Act. Through exclusive partnerships with esteemed hospitals worldwide, Garner Bio ensures access to a wide variety of biospecimens, facilitating pre-clinical trial sponsors' objectives for racial and ethnic diversity. Our commitment to excellence in compliance, partnership, and accessibility underscores our dedication to advancing DMD research and improving outcomes for patients worldwide. Contact us today to learn more. #Duchennemusculardystrophy #DMD #DMDresearch #DMDbiospecimens #raredisease #preclinicalresearch #clinicalresearch #Garnerbio #biospecimensourcing https://lnkd.in/dc2_pqeR

A Guide to Sourcing Biospecimen for Duchenne Muscular Dystrophy — Garner Biosolutions

A Guide to Sourcing Biospecimen for Duchenne Muscular Dystrophy — Garner Biosolutions

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