Health Science


Pharmaceutical companies, manufacturers of medical and surgical devices, clinical research organizations, biotech companies and healthcare managers trust Link Translation for translation of their most sensitive documents.

Translation for the Health Science industry requires multiple levels of quality control and a full understanding of stringent regulatory laws. The review process is critical to the quality of the translated product. Before starting your translation, we first screen and pre-select the most qualified SME translator verifying that their expertise matches exactly your type of content and your life-science field or sector.

Link translation provides medical translation for:

Biotechnology | Companies | Pharmaceutical Companies Organizations | Medical Devices Organizations | Clinical Research Organizations

Our human resources include linguists with training in most branches of medicine, biochemistry, biotechnology, chemistry, pharmacology and toxicology. We can provide translation certificates with each translation and if required by regulatory authorities, we can have your translated medical documents validated by medical doctors who are licensed in the target countries.

Our quality assurance for the health science industry also includes proofreading by an independent translator, project manager check, terminology approval by subject matter expert and back translation. We work only with professional, regularly tested and verified native-speaker translators who are Subject-Matter-Experts in a specific medical field.

Our unique methodology delivers consistently clear, accurate translation of high-value information, such as:

Adverse Effects
Product Case Report Forms (CRF)
Clinical Protocols
Clinical Trials
CRA Training Materials & Videos
Data Sheets
Drug Registration Documentation
Informed Consent Forms
Instructions for Use (IFU)
Investigator Brochures
Patient Information
Patient Report Outcomes (PRO)

Pharmacological Studies
Product Labels
Production Manuals
QoL Measures
Rater Scales
Regulatory Audit
SAE and SOP Procedures
Scientific Journal Articles
Software and Hardware
Manufacturing Process Descriptions
Master Batch Records
Deviation Reports
Marketing Collateral
Multimedia Audio and Visual