# Pharmaceuticals & medical devices

[Website page](https://verlineo.cc/industries/life-sciences) · en

This document reflects the public website. Starting rates are not a final quotation. Agreements for the individual project take precedence.

Regulatory submissions, clinical documentation and labelling for European markets.

Work is scoped around submission dates, with terminology governed by the authority's own standards.

Everything here is read twice: once by a regulator against its own templates, and once by a patient who has to understand it. Those two readers want different things from the same sentence, and reconciling them is most of the work.

- Terminology aligned to MedDRA, EDQM standard terms and the authority's own templates
- Separate readability checks on every patient-facing document
- Back-translation and reconciliation wherever the protocol calls for it
- A full audit trail of translator, reviser and approval dates

## Related pages

- [Medical & life-sciences translation](https://verlineo.cc/knowledge/en/service-life-sciences.md)
- [Technical & engineering documentation](https://verlineo.cc/knowledge/en/service-technical.md)

[llms.txt](https://verlineo.cc/llms.txt)