According to the Biotechnology Industry Organization (BIO), there are more than 300 biotech drug products and vaccines currently in clinical trials targeting more than 200 diseases, including various cancers, Alzheimer’s disease, heart disease, diabetes, multiple sclerosis, AIDS and arthritis.
As more and more clinical research and drug manufacturing is being done in multiple countries and in multiple languages, quality language services can help bring a biotech medical product to market faster and can help streamline the clinical trial process. Translation may be required at many stages, including clinical research, regulatory submission and review, production and marketing. Moreover, expansion of the EU block into new member countries is also driving increased demand for medical and pharmaceutical translation services.
GTS is a leading provider of specialized translation services to leading biotech companies and contract research organizations (CRO). The documents we translate include:
- Case Report Forms (CRF)
- Clinical Trial Materials
- Doctor Guides
- Drug Inserts
- Informed Consent Forms (ICF)
- Manufacturing Specifications
- Marketing materials and web content
- Patient Guides
- Patient Questionnaires
- Regulatory Documents
Customers in the Biotech, Medical Device and Healthcare industries have come to rely on our team of subject-matter experts for even the most complex translations. Our human resources include linguists with experience in genetics, biochemistry, biotechnology, chemistry, pharmacology, toxicology and more.