Your quality system passed its last audit. Then you sell into Canada and MDSAP becomes mandatory, a sponsor audit asks for ICH E6 R3, or your next product has software in it and IEC 62304 arrives with it. Most of what the new standard asks for, you are already doing. But the only way to find out which controls already answer it is a clause-by-clause review by hand.
Map once, comply everywhere
The standards life sciences companies are held to, mapped clause by clause. One evidence base across all of them. AI gap analysis that reruns whenever a record changes.
Pick a standard, upload an SOP, see the gaps · Your documents stay yours · No credit card

Every new standard, another evidence trail built by hand
Regulatory complexity multiplies as you grow
One standard becomes several
QMSR, ISO 13485, EU MDR, MDSAP, ICH, each with its own clause list and spreadsheet
Finding the gaps is a manual review
Someone reads every clause against every record, or you pay a consultant to.
The same evidence, standard by standard
Effort spent twice, and the gaps in the overlap are the ones an auditor finds first.
THE STAKES
Every standard you add costs months, consultants and headcount.
ONE EVIDENCE BASE, ASSESSED AGAINST EVERY STANDARD
Add a standard without starting over
Qualio breaks every standard down clause by clause and automatically assesses your records against each one.
One control can satisfy several standards at once, so when you add a standard you see what your existing controls already cover, what is new, and where the gaps overlap. And it reads the records where they live: in Qualio, in your document store, or in a QMS you already run.
How it works
Find it. Fix it. Prove it closed.
Choose the standard from the catalog, or build your own. Then point it at your policies and records: connect your QMS or document store, or upload the files yourself.
AI reads each record against each clause of the standard and returns findings. Every finding cites the clause it applied and the record it read.
Every finding carries a recommendation, and Copilot drafts the fix from it: the procedure update, the change control, the CAPA, the tasks for the people who own them. Your team reviews and approves.
A fix lands, a procedure is revised, a supplier is qualified. Qualio reassesses, confirms what closed, and flags what drifted.



Hear from our customers
“My confidence in being audit-ready is dramatically improved… one organized system that’s a lot easier to maintain.”
Chris Rice
Senior Quality Assurance Manager, AGADA Biosciences

“Before Qualio, the level of manual effort required to pursue new certifications meant we could only take on one standard per year. Now, we’re managing multiple frameworks simultaneously and staying ahead of them.”
Allison Iles
Quality Engineer, Cogstate

“Qualio gives us a 360-degree view of our compliance posture and automatically surfaces the gaps. We resolve issues faster, our team is more productive, and our risk is lower.”
Christophe Dohr
Site Quality Manager, Sentec

Purpose-built for life sciences
See it for your industry
See Qualio in action
Explore Qualio’s framework library
Tell us the standard you are most worried about. We will show you how Qualio addresses it, usually in the first conversation.
80% less audit prep time (Sentec)

