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Optimizing Clinical Data Registries: Opportunities for Diversity and Feasibility

H1 Blog

Without access to all the relevant data, researchers are unable to fully understand the complexities of diseases and develop effective treatments. This is especially true for registries outside of the United States where data is not as strictly regulated.

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Predictive Analytics in Clinical Trials

Vial

The fields of artificial intelligence (AI) and machine learning (ML) are increasingly influencing clinical research and development (R&D). Contract research organizations (CROs) and pharmaceutical companies can leverage these cutting-edge technologies to streamline clinical trials and introduce automation in drug discovery.

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Article EMA Thank You What we expect European regulators to do in June 2024

Agency IQ

What we expect European regulators to do in June 2024 In this recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods, and more.

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Codon Digest: Hackathon Prize Winners

Codon

A live demo is available online, but “it chews through OpenAI credits,” Patel says. Goodsell, Scripps Research and RCSB Protein Data Bank. There’s a live demo available online. “Right now, it can only make one protein at a time,” Gershon says, simply because the demo has limited compute resources.

DNA 52
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Codon Digest: Hackathon Prize Winners

Codon

A live demo is available online, but “it chews through OpenAI credits,” Patel says. Goodsell, Scripps Research and RCSB Protein Data Bank. There’s a live demo available online. “Right now, it can only make one protein at a time,” Gershon says, simply because the demo has limited compute resources.

DNA 52
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The Trust Fall: Building Successful & Diverse Trials Outside the U.S.

H1 Blog

Another challenge faced by international clinical trials is the lack of reliable data about local health systems and regulations. From legal considerations to data privacy regulations, the challenges facing these teams can be daunting. Additionally, clinical trials are no longer confined to one country or region.

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Article EMA Thank You What we expect European regulators to do in December 2023

Agency IQ

What we expect European regulators to do in December 2023 In this new recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations, comment periods, and more.