Professional Biotechnology Translation Services

GTS provides certified translation services for biotechnology companies, pharmaceuticals, and contract research organizations (CROs). Our native-speaking translators specialize in biotech content, ensuring accuracy and compliance with international standards. We offer fast delivery and ISO 17100:2015 certified quality to support your global research and development efforts.


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Expert Translation Solutions for the Biotech Industry

GTS is a certified provider of biotechnology translation services to leading biotech companies, pharmaceuticals and contract research organizations (CRO). We work in over 100 languages including French, Italian, German, Spanish, Chinese and Japanese. We also translate from any language into English. Click here to get an instant online quote for document translation services.

Trusted by the World’s Leading Biotech Companies

Over the years, GTS has provided professional translation services to some of the largest names in biotechnology, including Johnson & Johnson, Novartis, Pfizer, AstraZeneca, GSK, and Merck. Our proven experience working with global biotech leaders is a testament to our expertise, quality standards, and ability to meet the most rigorous regulatory requirements. When it comes to biotechnology translation, you can trust GTS to deliver excellence.

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.

Certified Quality and Compliance

Biotechnology Translation Services
GTS provides a complete solution for the translation requirements of biotechnology firms and companies in the life sciences

Our quality policy is certified as compliant with the ISO 17100:2015 standard. We provide signed Statement of Accuracy certificates with all translations. We can also provide back translation and validation when required by the IRB or regulatory authority.

Trends in Drug Development and Clinical Trials

The biotechnology industry continues to grow at an unprecedented rate, with advances in medical research and drug development driving this expansion. According to the latest data, the number of biotech drug products and vaccines in clinical trials has surged significantly. Now, according to the Biotechnology Industry Organization (BIO) over 400 biotech medical products are being tested for their efficacy against more than 250 diseases. These include not only traditional areas like various cancers, Alzheimer’s disease, heart disease, diabetes, multiple sclerosis, AIDS, and arthritis but also emerging health concerns such as rare genetic disorders and novel infectious diseases.

The global nature of clinical research and drug manufacturing adds a layer of complexity to the process. Today, these activities are often conducted in multiple countries, encompassing a wide range of languages and cultural contexts. This global dispersion underscores the crucial role of quality language services in the biotech sector. Effective translation and localization services are no longer just an optional support mechanism; they are integral to the successful development and deployment of biotech products.

Why Translation is Critical in Multinational Biotech Projects

Translation is essential at various stages of a biotech product’s lifecycle, including during clinical research, regulatory submissions, production, and marketing. The intricacies involved in accurately translating technical documentation, patient records, consent forms, and marketing materials make it a specialized and high-stakes field.

Translation for EU Compliance and International Standards

Furthermore, the evolving regulatory landscape, particularly within the European Union, demands rigorous compliance. The EU’s directives and regulations are constantly updated, necessitating meticulous translation services to ensure that biotech companies adhere to these standards. This regulatory evolution drives an increasing demand for skilled medical and pharmaceutical translation services, capable of navigating the complex web of international laws and guidelines.

Enabling Market Access and Accelerating Global Health Impact

As the biotechnology industry advances, the need for quality language services becomes more critical. These services not only expedite the process of bringing a medical product to market but also ensure adherence to international regulatory standards, ultimately facilitating global health advancements.

Biotechnology materials that we translate

The biotechnology translation services that GTS provides include translation in over 100 languages of:

  • Case Report Forms (CRF)
  • Clinical trial materials, clinical study agreements, clinical protocols
  • Informed Consent Forms (ICF)
  • Doctor Guides
  • Drug Inserts
  • Manufacturing Specifications
  • Marketing materials and web content
  • Patents
  • Patient Guides
  • Patient Questionnaires
  • Regulatory Documents