For pharma sponsors and CROs managing clinical vendor portfolios

Bring Drugs to Market Faster. Start With Your Vendors.

Mayet combines hands-on advisory with purpose-built software to make your vendor oversight audit-ready, efficient, and aligned with ICH E6(R3). Before your next inspection.

Explore our consulting services

Our Offerings

Advisory — Vendor Consulting

Get your vendor management where it needs to be

Led by Tom Lazenby, with a decade of clinical QA leadership. We assess your vendor oversight, identify E6(R3) gaps, and deliver an actionable roadmap.

Advisory investment credits toward a VendorVigilance subscription.

VendorVigilance

Operationalise your vendor oversight in a single, audit-ready system

Full visibility across your vendor portfolio, from selection through study closure. Eight integrated modules. 21 CFR Part 11 compliant.

Engineered for the way ICH E6(R3) expects you to work.

How It Works

Book a consultation

In one hour, Tom's team assesses your vendor oversight and identifies where you stand against E6(R3).

Receive your roadmap

A concrete, executable plan with improved SOPs, workflows, and oversight structures tailored to your organisation.

Execute

Implement with your existing tools, or take the next step with VendorVigilance. Advisory spend credits toward your subscription.

Why Teams Trust Mayet

Compliance as architecture

21 CFR Part 11. ICH E6(R3). GxP. These are not features added after launch. They are the foundation. Our software is engineered around regulatory requirements from the data model up.

Built by practitioners

Our CEO led clinical QA at GSK for a decade. Our CTO and CPO have built regulated SaaS together for 19 years.

Advisory + software, together

Most consultancies deliver a report and move on. Mayet delivers a roadmap you can execute, and VendorVigilance picks up where Advisory leaves off.

Purpose-built and focused

One thing done well: helping pharma and biotech teams manage vendors and run clinical trials with confidence.

"Tom consistently went above and beyond. Proactive support, insightful recommendations, and a level of dedication that truly stood out. We're grateful for the clarity and confidence they brought to our transformation journey."
— Sam Taylor, EVP Proposals, Evestia Clinical

Also From Mayet

TrialTrack

GxP-Ready Project Management for Clinical Teams

Spreadsheets, Trello, and Smartsheet were not built for regulated clinical work. TrialTrack gives small pharma and biotech teams a compliant project management system for studies, sites, and participants. No enterprise CTMS cost or complexity.

Free tier available. Same-day adoption. Compliance built in from day one.

Start With a Conversation

Book a free one-hour consultation with Tom. You will know where your vendor management stands against E6(R3), and what to do about it.

No commitment required.