Pharmaceutical Translations

ISO-certified translations

When it comes to the pharmaceutical industry we understand that accuracy and quality could make or break your company. Our expert translators are fully equipped to help amplify your global reach by tailoring your text to different territories while sticking to the language that this complex industry demands.

Every translation Transcripta signs off is peer-reviewed and ISO certified, and produced in line with the strict standards set by the appropriate regulatory bodies in whichever part of the world you are looking to market to, so you can rest easy knowing we have taken care of the details.

Taking pharmaceuticals global

Our awesome experts are specifically trained to handle any medical or pharmaceutical translations, from clinical trials all the way through to marketing materials to take your newest medication to the global market.

We are proficient at translating every kind of content you can find in this fascinating industry, including:

  • Training materials
  • Medical labels
  • Product summaries
  • Patient leaflets
  • Informed consent forms
  • Insurance forms
  • Registration documents
  • Marketing collateral
  • Full, SEO-ready websites
  • Patents
  • Medical journals

Accuracy matters

The nature of this hugely important industry means that accuracy in your translations is not just crucial in terms of marketing and understanding medications — it could literally save consumers’ lives. From groundbreaking clinical studies and research to developing, testing, and distributing life-changing medicine across the globe, clarity is key in any language.

Language saves lives

We understand the strict regulations that keep the pharmaceutical industry safe and combine that keen understanding with any language we use. Living in an increasingly more globalised society means that policies, laws and government regulations are rapidly changing to keep up and keep people safe.

Transcripta has over 15 years’ experience of translating EPAR reports for the European Medicines Authority (EMA) and SPCs for pharmaceutical companies. Our team is well-acquainted with QRD templates and terminology approved by EMA. We stay abreast of developments by attending industry events and constantly refining our glossaries to make sure materials align with the latest practices.

Get in touch

We speak your language. Contact us for a quote today.

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