Quality controlled accurate and authoritative translation for pharmaceutical companies, clinical trial organisations, and medical equipment manufacturers both large and small.
Communication is the driving force behind progress. But if we are unable to communicate effectively across all nationalities, languages, and cultures, we not only limit our ability to progress; we risk being misinterpreted, misrepresented, and misunderstood.
There are few fields where this requirement is as significant as those of medicine, clinical research, and pharmaceuticals.
The health and wellbeing of patients and the success of healthcare organisations hinges on the clarity and accuracy of its documentation.
At Oliver Translations, we believe that the language into which a text is translated should never prove a barrier to its quality and accuracy: with no nuance lost, or any instruction subject to uncertainty.
Our translators are hand-picked for their expertise not just in the source and target language of your documentation, but also for their expertise, qualification and experience in their respective medical and pharmaceutical fields.
We work closely with a highly professional network of both specialist medical translators and companies who cover a wide range of languages and subject matter.
We are a Corporate Member of the Institute of Translation and Interpreting (ITI)
Our quality management system is ISO 17100 certified, the European Standard for translation. Read more…
Anaesthesia
Allergology and Immunology
Audiology
Biomedicine
Emergency medicine
Gerontology
Histopathology
Medical devices
Obstetrics and gynaecology
Oncology
Paediatrics
Pathology
Plastic and reconstructive surgery
Psychiatry
Rehabilitation medicine
Rheumatology
Surgery
Virology
Medical reports
Clinic brochures
Patient information leaflets (PILs)
Pharmaceutical product labels
Clinical outcomes assessments
Medical articles
Clinical study documents
Chemical translations
Scientific publications
Summary of Product Characteristics (SPCs)
Ethics committee letters
Reports of adverse effects
Discharge letters
SOPs
Manufacturing instructions and protocols
Product marketing
ISO 17100 certification
Rigorous proofreading of each translated document by a third party
Stringent quality controls by independent reviewers and revisers
Complete project management from start to finish
Native speakers used wherever possible – or individuals with an in-depth knowledge of the target language
We use translators with a specialised knowledge of your subject area
Fast turnarounds
Constant and effective communication with you throughout
Back translation
Post-submission editing