Our medical linguists often come from clinical, pharmaceutical, regulatory, and public health backgrounds. They understand the terminology, the risks, and the real-world consequences of every word.

We translate:

• Patient Information Leaflets (PILs) and Instructions for Use (IFUs)

• Informed Consent Forms (ICFs) and Ethics Committee submissions

• Clinical trial documentation: protocols, CRFs, SAE/SUSAR reports

• Regulatory submissions (EMA, FDA, MHRA, PMDA)

• Medical device labelling, packaging, and technical files

• Pharmacovigilance content and adverse event reporting

• Public health materials and behaviour change campaigns

• Hospital records, diagnostics, and discharge summaries

• Medical marketing and training content

We combine best practice with global standards and meticulous quality checks to keep your content accurate.

Certified to:

• ISO 17100 (translation services)
• ISO 9001 (quality management systems)

Aligned with:

• ISO 18587 (post-editing of machine translations)
• ISO 13485 (medical devices)
• ISO 14001 (environmental management systems)

Members of:

• UN Global Compact
• Institute of Scientific and Technical Communicators (ISTC)
• Institute of Sustainability and Environmental Practice (ISEP)
• Professional Society for Health Economics and Outcomes Research (ISPOR)
• Association of Translation Companies (ATC)

• Pharmaceuticals and biotechnology

• Clinical trials and CROs

• Medical devices and diagnostics

• Hospitals, clinics, and healthcare providers

• Public health and not-for-profit organisations

• Regulatory affairs and compliance consultants

• Health economics and outcomes research (HEOR)