What we do
Validation services that scale from one system to a full portfolio.
Every engagement starts the same way — risk first, paperwork second. What follows depends on what you're validating.
Overview
Validation across every layer of a regulated operation.
We don't just validate software — we cover the full range of GxP-impacting systems, processes, products, and equipment.
IT systems validation
Enterprise applications, cloud platforms, and infrastructure — from Veeva and Salesforce to AWS and internal tooling — validated to GxP standards without slowing your release calendar.
Process validation
Validation of the procedures and workflows that govern how regulated work actually gets done, so process changes hold up under audit.
Product validation
Validation support across the product lifecycle, aligned to the quality and regulatory requirements your product is held to.
Equipment validation (lab & manufacturing)
Qualification of laboratory and manufacturing equipment — installation, operational, and performance qualification (IQ/OQ/PQ) built around actual use conditions.
Strategy first
Master Validation Plans & strategy.
Before anything gets scripted or tested, we build the roadmap — what needs validating, in what order, to what depth, and why. A Master Validation Plan gives your team (and your auditors) a single source of truth for how your validation program is governed, so individual projects aren't reinventing the approach every time.
The differentiator
Validation Accelerator Packs.
Our biggest time-saver: pre-built, pre-scripted validation packages for the platforms life sciences companies already run — Veeva, Salesforce, ServiceNow, AWS, Snowflake, and more. Instead of starting from a blank URS every time a system needs validating, our accelerator packs give you a proven starting point, cutting typical validation timelines by up to 60%.
Independent oversight
Independent Verification & Validation (IV&V).
An independent set of eyes on your validation program — verifying that what was built matches what was specified, and that what was tested actually proves the system works as intended. IV&V is one of the fastest-growing needs in FDA-regulated industries, and it's a core part of how Mayona supports clients who need validation rigor their own team can't self-certify.
Not sure which service fits?
Tell us what you're running and we'll map it to the right starting point — strategy, accelerator pack, or independent review.