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Discussing the future of precision medicine.

Level Up your Documentation Processes and Systems to Comply with FDA Final Rule Stages 1 & 2

FDA’s ruling on enforcement of in vitro diagnostic (IVD) medical device requirements for laboratory-developed tests (LDTs) was published in May of 2024. Barring delays from legal or legislative action, enforcement of Stage 1 will begin in 9 months. W...
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Get Ready to Comply with FDA Final Rule Stages 1 & 2: Yeah, We Mean You

FDA's New LDT Rule: An Overview
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Navigating your molecular lab’s test selection and development over the next two years

With the FDA’s publication of the final rule on laboratory developed tests (LDTs) on May 6, 2024, cl...
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Four Years, Five Stages: the FDA's Final Rule on LDTs

After over a decade-long saga, the Food and Drug Administration (FDA) published its final rule on La...
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Meeting the NIH Data Management and Sharing (DMS) policy requirements

The Velsera suite of NIH-funded platforms including Cancer Genomics Cloud (CGC), BioData Catalyst Po...
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Highly Customizable Multi-sample Single Cell RNA-Seq Pipeline on CGC

The reasons and rationale behind single-cell RNA-Seq “To study human biology, we must know our cells...
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