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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/NyquistAI
NyquistAI

NyquistAI

Founded 2020

Analyze global clinical trials, medical device records, and drug data for life sciences research

Pricing model

Paid

You can use Nyquist AI to search and analyze vast amounts of global life sciences data, including clinical trials, medical device approvals, and drug records. It reviews medical literature to identify relevant research papers, allowing you to ask questions and extract answers directly from scientific studies. The system aggregates regulatory records and adverse event reports across major markets like the US, EU, and China. Teams use it to accelerate market research, monitor product safety, support regulatory filings, and track competitor developments across the healthcare sector.

What NyquistAI does

Search medical device predicate historiesQuery adverse event databasesScreen literature for clinical evaluation reportsChat with scientific research papersExtract clinical trial outcome summariesCompare drug approval timelines across regionsTrack safety reports from global health authoritiesAccess to data on over 770,000 clinical trials worldwideDatabase covering more than 3 million approved medical devicesGlobal regulatory coverage across the US, EU, China, Japan, and other marketsScreening tool to review and select research papers for medical writingChat interface to query and extract findings from scientific papersSearchable repository of over 26 million adverse event reportsAutomated summarization and data synthesis from complex medical reports

Pricing breakdown

Pricing model: Paid

PlanList price
Pharma (per seat)$299 / mo
Pharma (per seat) (annual billing)$239 / mo, billed annually
MedTech (per seat)$349 / mo
MedTech (per seat) (annual billing)$279 / mo, billed annually
All Access (per seat)$459 / mo
All Access (per seat) (annual billing)$367 / mo, billed annually

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Nyquist AI, life sciences data, clinical trials, medical devices, medtech intelligence, pharma intelligence, FDA MAUDE database, medical writing screening, adverse event reports, regulatory intelligence, healthcare data, drug approvals, literature review, clinical research