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Built for ops-led teams pursuing or maintaining ISO 9001 or ISO 27001, not a regulated-industry eQMS.
Most teams pursuing ISO 9001 or ISO 27001 end up with a quality manual and a folder of procedures that nobody opens between audits. The documentation exists, but you cannot prove anyone read the current version, and when the auditor arrives, prep turns into a fire drill. Waybook closes the gap between documented and followed: every procedure is assigned to the people who do the work, and you can see at a glance who has read it and who has not.
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Keep your whole QMS in one system, not scattered across Word files and shared drives. Every procedure is assigned to a role, read-confirmed, and version-controlled, so the only version your team sees is the current one and the read history becomes audit evidence. Draft procedures with the free AI SOP and procedure builder or import what you have. Your ISO procedures are SOPs at heart, and Waybook is the SOP software for growing teams built to run them.
ISO 9001 covers quality management and ISO 27001 covers information security, but they share the same management-system structure, called Annex SL. That means document control, internal audits, and training records work the same way for both. If you are pursuing or maintaining both standards, you keep both document sets in one place, each assigned and read-confirmed, instead of running two parallel systems that drift apart.
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Your QMS does not live on an island. An ISO procedure is a process, the steps inside it are tasks, and every new starter has to learn them. Waybook keeps them in one stack: your procedures, the work instruction software for task-level steps, your process documentation software, and onboarding built on the same documents your auditors will check. One connected stack, not four disconnected tools.
ISO is not just for factories. Professional services keep client-delivery procedures consistent, SaaS teams read-confirm their ISO 27001 access and data policies, engineering firms run calibration and inspection procedures, and healthcare teams keep care protocols current with an audit trail. Waybook is not a validated eQMS for regulated manufacturing or medical devices (for ISO 13485 or pharma GxP, choose a dedicated eQMS), but for ops-led teams running ISO 9001 or ISO 27001 it is where the documentation lives and gets followed.
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| Tool | Best for | Team follows it | Pricing | Best suited for |
|---|---|---|---|---|
| Waybook | Ops-led teams (20 to 200) running ISO 9001 or ISO 27001 without a regulated-industry eQMS |  | From $99/mo | Teams that need ISO documentation assigned, read-confirmed, and kept current, linked to their SOPs |
| Dedicated eQMS suite | Regulated manufacturing, pharma, and medical devices that need CAPA, nonconformance, e-signatures, and validation | | Enterprise / quote | Regulated industries that need a validated eQMS and can carry the admin and cost |
| Word, SharePoint or Drive | Getting started, smallest teams |  | Free / included | The earliest stage, before proof of who read what matters |
QMS software (quality management system software) is where a team documents, assigns, and tracks the procedures that keep its work consistent and audit-ready. Instead of a quality manual and procedures sitting in Word files and folders, everything lives in one system: assigned to the roles that do the work, read-confirmed, and version-controlled. For teams running ISO 9001 or ISO 27001, the documentation auditors ask for stays current, controlled, and provable in a few clicks. Waybook is quality management system software built for ops-led teams who need their ISO documentation followed, not just filed.
No. You can run a quality management system in Word and a shared drive, and plenty of small teams do. The problem is proof. Auditors check that staff follow the current version of a procedure, and a folder cannot show who read what or which version is live. Software earns its place when version control, role assignment, and read confirmations need to be audit evidence on demand rather than a manual scramble before every audit. If your ISO documentation drifts out of date or you cannot prove people have read it, that is the signal you have outgrown files and folders.
No, and that is deliberate. Waybook is where your QMS documentation lives and gets followed. It is not a validated eQMS with built-in CAPA, nonconformance, or electronic-signature workflows for regulated industries. If you make medical devices (ISO 13485) or work under pharma GxP, a dedicated eQMS is the right tool. For ops-led teams running ISO 9001 or ISO 27001 who need their procedures, policies, and checklists assigned, read-confirmed, and kept current, Waybook fits without the cost and admin of a regulated-industry suite.
Yes. ISO 9001 covers quality and ISO 27001 covers information security, but both are built on the same management-system structure, called Annex SL. Document control, internal audits, management review, and training records work the same way for both standards. In Waybook you keep both document sets in one place, each procedure and policy assigned to the right roles and read-confirmed, so a team pursuing both certifications runs one system instead of two that fall out of sync.
Auditors look for two things: that your documents are current and controlled, and that staff actually follow them. In Waybook every procedure has a version history and a record of who has read and confirmed it, so the evidence an auditor asks for is a few clicks rather than a fire drill. Because the current version is the only version your team sees, you avoid the most common finding of all, which is people working from an out-of-date document. Keeping the QMS live all year also means surveillance audits stop being a yearly re-do.
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