Translation services and multilingual content management for the life sciences
Trans4Europe offers specialized language solutions for the life sciences, covering thepharmaceutical industry, medical device manufacturing and clinical research.
We ensure the accurate translation and efficient management of your international content, in compliance with the strict regulatory standards specific to this sector.
Over 18 years’ expertise in translation and content management for the life sciences
With over 18 years’ experience, Trans4Europe is a recognized leader in specialized translation and international content management services for the life sciences sector.
We understand the critical importance of your field, and tailor our technology solutions and services to meet stringent regulatory, validation and local and cultural compliance standards.
We work closely with medical device manufacturers, pharmaceutical laboratories, biotech companies and medical research centers, providing them with high-quality language services, in-depth industry expertise and in-depth knowledge of scientific issues.
Regulatory compliance and linguistic quality throughout the life cycle of pharmaceutical products
In a constantly evolving pharmaceutical and biotechnology sector subject to strict regulations, regulatory compliance, quality,integrity, traceability and patient safety are essential for international success.
At Trans4Europe, we meet your specific linguistic needs at every stage of your products’ life cycle, from pre-clinical phase to post-market surveillance, guaranteeing accurate, compliant and adapted translations.
✓ Translations for clinical trials
✓ Meeting regulatory submission deadlines
✓ Marketing communication
✓ Patient recruitment
✓ Timely pharmacovigilance reports
✓ Translation of manufacturing documents
✓ Corporate communications (HR, legal, training)
Rigorous translation and linguistic validation for clinical trials
Clinical trials are subject to strict regulations and encompass a variety of critical documents, such as Clinical Outcome Assessments (COAs), Patient-Reported Outcomes (PROs), Physician-Reported Outcomes (ClinROs) and Observer-Reported Outcomes (ObsROs).
These requirements call for a complex, rigorous translation and linguistic validation process in line with international standards, to ensure the accuracy and reliability of multilingual clinical data.
✓ Coordination of multilingual studies
✓ Translation for clinical trials
✓ Patient search and recruitment
✓ Language validation
✓ Technology and process consulting
✓ Timely pharmacovigilance reports
✓ Translation of manufacturing documents
✓ Corporate communications (HR, legal, training)
Accurate and compliant translation of medical device content
Whether for healthcare professionals or patients, medical devices are accompanied by instructions, labels, packaging and other essential content.
Excellence in translation is crucial to ensure the correct and safe use of devices, while ensuring compliance with local and regional regulatory requirements.
Trans4Europe supports you with specialized language services, tailored to the strict standards of the medical device industry.
✓ Coordination of multilingual studies
✓ Translation for clinical trials
✓ Patient search and recruitment
✓ Language validation
✓ Technology and process consulting
Your dedicated team of native language experts ensures cultural and linguistic accuracy while complying with current regulations 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, etc.
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.
