Integration of Technology, Process and Quality Control: Protecting Complete Sample Chain of Custody

Implementation of biobanking best practices and analytical platform standardization are two important components for any data generation associated with state of the art biobanks that support precision medicine applications. Sample collection, pre analytical variables, controlled environment storage and sample processing can often have a large impact on the quality of biomaterials. This roundtable will describe how to standardize biobanking efforts in a manner commensurate with both academic and industrial partnerships. Data will be presented on the governance of biosample collections, standardization efforts, and quality control harmonization for biosamples as well as global best practices for the regulatory oversight of national and commercial biobank resources. Finally, a review of several international programs will illustrate how collaborative efforts are helping advance integrated biobanking precision medicine across many research and clinical areas.
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OTHER ON-DEMAND WEBINARS

Genomics and the Future of Human Reproduction

Ambry Genetics

For most of humanity’s existence, we had only one way to make babies. The last century or so have seen the beginnings of change, with artificial insemination, in vitro fertilization, and prenatal and preimplantation genetic testing. The rest of this century will see astonishing changes, made both possible and attractive by genomics – from embryo selection to embryo editing, from mitochondrial transfer to human reproductive cloning, to in vitro gametogenesis, and beyond. This talk will survey those changes and point out some of their likely ethical, legal, and social implications.
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Principles of Transporter Drug Interactions with Special Focus on Hepatic and BBB Transporters

solvobiotech

Transporters are involved in clinically significant drug-drug interactions (DDI). Such interactions can occur at multiple sites, including in organs important in drug absorption (e.g. intestine), elimination (e.g. liver and kidneys) and distribution (e.g. brain). Notably, some of these interactions can be “hidden”, occurring in a tissue with no discernible trace in the systemic circulation. In addition, for drugs that are both transported and metabolized, DDI will most prominent when they occur at the “rate-limiting step” in the clearance of the drug.
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Verification of Autoantibody Serology Tests: Practical Considerations for the Clinical Laboratory

Autoantibody assays may have significant differences due to the heterogeneity of autoantibodies, including epitope specificity, isotype, and affinity/avidity.
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Genome Editing Tools: Beyond Discovery

Developing new CRISPR/Cas9-based genome editing tools will enhance innovative therapeutic products and the pathway to clinical programs. However, current obstacles in genome editing include high error rates, toxicity from production impurities, and strict regulatory concerns.
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