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, so your vendor oversight is audit-ready and aligned with ICH E6(R3) before your next inspection.

See Vendor Advisory packages

Advisory to fix the process, software to run it

Vendor Advisory

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.

Vendor Advisory fees are credited toward a VendorVigilance subscription.

VendorVigilance

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

See your whole vendor portfolio, from selection through study closure, across eight integrated modules. 21 CFR Part 11 compliant.

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

From first call to working process

Book a consultation

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

Receive your roadmap

An executable plan covering the SOPs, workflows and oversight structures your organisation needs to change.

Execute

Implement with your existing tools, or take the next step with VendorVigilance. Vendor Advisory fees are credited toward your subscription.

Why teams trust Mayet

Compliance as architecture

We design our software around 21 CFR Part 11, ICH E6(R3) and GxP from the data model up, instead of adding compliance after launch.

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.

Vendor Advisory and software, together

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

Only pharma and biotech

We build for pharma and biotech and nothing else: vendor oversight, clinical project management, and the regulations around both.

"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.

There's a free tier, and teams can start using it the same day.

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.