USA
UKTranslation Services for Healthcare & Pharmaceuticals
- ISO 17100
- ITI
- CIOL
- UKVI Accepted
The healthcare and pharmaceutical industries operate under regulatory frameworks where translation accuracy is a patient safety requirement. An MHRA submission with incorrectly translated clinical data can delay drug approval. A mistranslated patient information leaflet can cause medication errors. A clinical trial protocol translated without ICH-GCP rigour can compromise trial integrity.
Translation AZ serves pharmaceutical companies, NHS trusts, private hospitals, CROs, medical device manufacturers, and biotech firms with certified medical and pharmaceutical translation from our London office. Every medical translation is performed by a linguist with clinical or life sciences expertise.
Documents We Translate
Clinical trials
Protocols, ICFs, CRFs, PROMs, CSRs, adverse event reports, and IRB/REC submissions
Regulatory submissions
MHRA marketing authorisations, SmPCs, PILs, and pharmacovigilance documents
Pharmaceutical labeling
SmPCs, PILs, primary and secondary packaging, IMP labeling
Medical devices
IFUs, device labeling, technical files, UKCA/CE marking documentation, and clinical evaluation reports
Patient records and medical reports
Discharge summaries, pathology reports, radiology reports, medical histories
Informed consent and patient materials
Consent forms, patient education, health literacy materials, and hospital signage
Healthcare compliance
CQC policies, NHS trust documentation, infection control
Why Healthcare Organisations Choose Translation AZ
Clinical and life sciences expertise β Translators with backgrounds in medicine, pharmacy, nursing, and biomedical sciences
Linguistic validation β Full linguistic validation workflow for PROMs and COAs: forward translation, back-translation, cognitive debriefing, harmonisation
UK GDPR compliance β Data processing agreements, encrypted handling, UK GDPR-trained staff
DTP for pharmaceutical packaging β Multilingual labeling with text expansion management, print-ready file delivery
Safety report urgency β Expedited turnaround for adverse event reports and safety-critical translations
Insurance coverage β Professional Indemnity and Cyber Liability insurance for healthcare translation
How It Works
Submit your documents
Upload through our secure, encrypted quote form. Include the regulatory context and therapeutic area.
Quote within 2 hours
With specialist linguist assignment and regulatory compliance confirmation.
Translation and review
Clinical/pharmaceutical specialist with independent review. PROMs undergo full linguistic validation.
Certified delivery
Version-controlled, regulatory-formatted, with certification.
2-Hour Quote Response β Standard 24β72 hrs Β· Rush available
Need Healthcare or Pharmaceutical Translation?
Submit your documents for a free quote. We respond within 2 hours.
Frequently Asked Questions
Yes. Our medical translators hold qualifications or demonstrated expertise in medicine, pharmacy, nursing, biomedical sciences, or related fields.
Yes. Data processing agreements, encrypted transmission, and UK GDPR-trained staff.
Yes. We support MHRA submission timelines with expedited turnaround for regulatory-critical documents.
Yes. Full linguistic validation: forward translation, reconciliation, back-translation, clinician review, cognitive debriefing, and harmonisation.