Mayet gives sponsors, CROs, and biotech teams the software and advisory services they need to run clinical programmes without the spreadsheet chaos, the audit-prep scramble, or the siloed oversight that slows everything else down.

Why Mayet, and what's in it for you?

🔹 Built by practitioners, not vendors. Our founders ran clinical QA inside pharma. Every feature in every product starts with the question "what would have made my job easier when I was managing fifty studies?" That's in it for you: software that matches the way you actually work, not the way a category-leader slide deck imagined you work.

🔹 Advisory and software, engineered together. Most tools leave you to figure out the operating model yourself. Mayet pairs purpose-built products with senior advisory input on ICH E6(R3), vendor oversight, and development strategy from day one. What's in it for you: executable roadmaps alongside the platforms that let you execute them, not two procurements stitched together.

🔹 Inspection readiness as the default state. Our products are built around ALCOA++, 21 CFR Part 11, Annex 11, and the ICH E6(R3) oversight model, so the evidence trail assembles itself as your team works. What's in it for you: less time assembling evidence for inspections, more time on the decisions that move the programme forward.

Explore our offerings:
- Advisory and consulting: https://mayetrx.com/consulting/
- VendorVigilance (vendor oversight for sponsors and CROs): https://vendorvigilance.net
- TrialTrack (clinical trial management for small pharma, biotech, and CROs): https://trialtrack.net

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