Pharma Industries
- Translation of safety data sheets
- Translations of summaries of product characteries
- Certified translations for marketing authorisation
Certified translations and
regulatory compliance
Obtaining marketing authorization from the European Medicines Agency (EMA) for veterinary drugs is a complex process that involves adhering to rigorous standards. In our translations, we use QRD templates, standard terms from the European Pharmacopoeia (EDQM), the INN search database, and the MedDRA dictionary. These resources enable us to deliver content that aligns with the demanding requirements of the EMA, ensuring the necessary accuracy and coherence in documentation.
Additionally, we extend our services to offer sworn translations of your product documentation in all 24 official languages of the European Union. This added capability ensures that your documentation not only aligns with regulatory requirements but also meets linguistic standards, streamlining the marketing authorization process within the EU.
We take pride in being your dedicated partner throughout this challenging journey and are eager to delve into the specific intricacies of your project. Don’t hesitate to reach out to us; we welcome the opportunity to initiate a discussion on how we can play a pivotal role in the success of your project within the realm of veterinary drugs!
Don’t hesitate to contact us if you are looking for a dedicated partner to navigate the intricate landscape of technical content within the veterinary field. We look forward to the opportunity to collaborate with you on achieving your project goals.
Contact us
We’re here to help! If you have any questions, comments, or suggestions, feel free to get in touch with us.