International translation and content management services dedicated to the life sciences, covering the pharmaceutical industry, medical device manufacturing and clinical research.
With over 18 years’ experience, Trans4Europe is at the forefront of high-quality translation and content management services in the life sciences sector. We fully recognize the importance of your business activity. That’s why our technology solutions and services are specifically designed to meet the industry’s most stringent standards in terms of regulation, validation and compliance with local and cultural requirements.
We work closely with medical device manufacturers, pharmaceutical laboratories, biotech and medical research companies, providing them with the highest quality language and content services, as well as unrivaled expertise and in-depth industry knowledge.
In the highly regulated and ever-changing environment of the pharmaceutical and biotechnology industry, regulatory compliance, quality, integrity, traceability and patient safety are crucial to successful international expansion. At Trans4Europe, we’re ready to meet your specific language requirements throughout the product lifecycle, from the pre-clinical phase to post-market surveillance.
✓ Translations for clinical trials
✓ Compliance with regulatory submission deadlines
✓ Marketing communication
✓ Patient recruitment
✓ Timely pharmacovigilance reports
✓ Translation of manufacturing documents
✓ Corporate communications (HR, legal, training)
Clinical trials are subject to very strict regulations and involve a multitude of documents such as clinical outcome assessments (COAs), patient-reported outcomes (PROs), clinician-reported outcomes (ClinROs) and observer-reported outcomes (ObsROs). This requires a complex process of translation and linguistic validation.
✓ Coordination of multilingual studies
✓ Translation for clinical trials
✓ Patient sourcing and recruitment
✓ Language validation
✓ Technology and process consulting
✓ Timely pharmacovigilance reports
✓ Translation of manufacturing documents
✓ Corporate communications (HR, legal, training)
Whether for healthcare professionals or patients, medical devices are always accompanied by instructions, labels, packaging or other essential content. Excellent translations are crucial, ensuring not only correct and safe use of devices, but also compliance with local and regional regulatory requirements.
✓ Coordination of multilingual studies
✓ Translation for clinical trials
✓ Patient sourcing and recruitment
✓ Language validation
✓ Technology and process consulting
Your dedicated team of native-language language experts ensures cultural and linguistic accuracy while respecting the regulations in force in the medical sector. Our project managers are responsible for training the team, monitoring compliance and adapting translation solutions to standards such as ICH MedDRA.
Break down language barriers with the expertise of Trans4Europe. Whatever the nature of your project, Trans4Europe will work with you to create a solution tailored to your needs.
© 2024 Trans4Europe All rights reserved.
© 2024 Trans4Europe All rights reserved.
