# Product data under control. Without enterprise PDM complexity.

Keep CAD files, documents, revisions, approvals and product data connected, so everyone works from the right information.

- **One source of truth**: No more hunting for the latest revision.
- **Controlled change**: Approvals, revisions and release history built in.
- **Built for engineering teams**: CAD, documents, BOM-related data, quality and suppliers, all connected.

## Built for regulated hardware

neo does not make you compliant on its own. It produces the records these frameworks ask for as part of everyday work.

- **21 CFR Part 11**: Validated e-signatures and audit trails designed to meet the requirements for electronic records.
- **ISO 13485**: Document and record control for medical devices: approval before use, revision status and retained history.
- **ISO 9001**: Control of documented information, with changes identified and approved before release.
- **EU Cyber Resilience Act**: Technical documentation and SBOMs versioned, approved and linked to the product revision they describe.

Your data: hosted in the EU, field-level encryption, granular permissions, complete audit logs, and you can export all of it at any time.

## Pay per seat, mix seat types as you need

Each person gets the seat that matches how they work with product data. Start with a free 3-month pilot. [Read more](https://neopdm.com/en/pricing)