An audit or inspection is coming up.
We check the documents in scope against the regulations you'll be inspected on, and against each other. Each finding points to the section and requirement behind it.
What we findFind the gaps before the auditor does.
We find gaps, contradictions, duplication and risks in your SOPs, policies and other regulatory documents. Then we make sure they stay up to date as regulations change.
Founders' backgrounds
CombinatorY Combinator
AuditThread / Document reviewExample from open text
Document excerpt§23 · Monitoring and audit
Frequency and plans for auditing trial conduct
Monitoring and audits will be conducted by University Hospitals Bristol and Weston NHS Foundation Trust (UHBW), on behalf of the Sponsor, and will ensure adherence to ICH GCP (International Conference on Harmonisation for Good Clinical Practice) and the aforementioned regulations. All trial-related documents will be made available on request for monitoring and audit by the Sponsor, the relevant REC and for inspection by MHRA and other licensing bodies.
A Trial Monitoring Plan has been developed by the Sponsors and agreed upon by the TMG and CI based on the trial risk assessment which may include on-site monitoring. Monitoring will be initiated using a risk-based approach.
How we work
From your documents to a review your team can use.
Pick the documents
Choose a document set and the rules and related procedures that it needs to meet.
Review stage
Get a step-by-step review using our trained Model.
Decide what to revisit
Agree what to check again when a document or a rule changes.
Illustrative workflow
A traceable path from source to decision.
01 / INPUT
Your documents
Procedure or policyApplicable requirements
02 / REVIEW
Suggested finding
Passage, issue and cited source together.
03 / DECISION
Human-in-the-loop
Confirm, amend or reject the finding.
Where to start
Start with one process.
AuditThread will keep it current for you.
Documents and regulatory requirements can change
A revised SOP or new guidance can open a gap in your documents. We make sure you are still ready for your audits whenever they come.
How an engagement worksWhat we find
Compliance is 24/7.
So are our models.
Your team knows the rules. The risk sits in whatever has changed since the last review or documents contradicting each other without anyone noticing.
Find the gaps
We set AuditThread up for the regulations and guidance you must meet, such as MHRA, EMA or FDA pharmacovigilance requirements. It checks your SOPs, policies and work instructions against them, and against each other, for gaps, contradictions, duplication and risks.
Stay current
Documents get revised and regulations change. We re-check when either does, to help you stay compliant between audits, not just before them.
Check our work
Every finding can be tracked to its source for any auditor to check. Our evals platform tests the AI model on documents with known issues, and records what it catches, misses and invents. The model improves with each review but the final call remains with humans.
The team
Oleg Giberstein
Co-founded Coinrule, an automated trading platform backed by Y Combinator, and ran it as COO for eight years, growing it to 350,000+ users. Previously in banking and risk at Citi. Studied at Oxford.
Conor Svensson
Founded Web3 Labs and created Web3j, the open-source Ethereum library with over 4 million monthly downloads. Built regulatory and trading systems at ANZ, UBS and Deutsche Bank.
Book a demo.
Tell us which regulations you work to and which documents you'd check first. We'll show you how AuditThread finds the gaps, and how we test what it finds.