ABOUT

I provide English-to-French translation services for medical and pharmaceutical documents used in regulated environments, primarily in the medical device and pharmaceutical sectors.

Types of documents handled:

• Instructions for use and user manuals (IFU)

• Technical and quality documentation

• Regulatory files and related documents

• Medical and pharmaceutical materials for internal or external use

Scope of work:

I do not provide regulatory consulting, clinical validation, or original medical writing. My role is strictly limited to the linguistic translation of existing documents, within the framework defined by the client.

Working languages:

Translation from English into French.

Collaboration:

For any enquiry or quotation request, a preliminary exchange helps define the scope, timeline, and constraints of the project. See the “Contact” section.