Clinical Trials Translation Services in Poland, Germany, and France
Accurate. Compliant. Trusted by Global Pharma Leaders.
At Prism Translation Services, we specialize in Clinical Trials Translation Services for leading pharmaceutical companies, CROs, biotech firms, and research institutions across Poland, Germany, and France. We ensure that your clinical trial documentation is accurately translated and fully compliant with EU medical regulations, EMA standards, and local health authorities’ requirements.
Multilingual Support for Clinical Research Across Europe
Whether you’re conducting Phase I to Phase IV trials, expanding into European markets, or submitting documents to regulatory bodies, Prism Translation Services offers expert linguistic support with subject-matter accuracy in over 100 languages, including Polish, German, and French.
Our certified medical translators ensure that your clinical research content is clear, compliant, and culturally adapted for successful regulatory approval.
What We Translate
At Prism, we provide certified clinical translation for a wide range of critical documents:
Clinical Trial Protocols
Investigator Brochures (IBs)
Informed Consent Forms (ICFs)
Case Report Forms (CRFs)
Patient Information Leaflets
Ethics Committee Submissions
Regulatory Submissions (EMA, ANSM, BfArM, URPL)
Adverse Event Reports and Safety Data
Clinical Study Reports (CSRs)
Quality of Life Questionnaires (QoL)
Poland – A Fast-Growing Hub for Clinical Trials
Poland is one of Europe’s most reliable destinations for conducting international clinical research. With strong healthcare infrastructure and cost-efficiency, clinical trial translations in Poland are in high demand. Prism Translation Services ensures translations meet URPL and EU guidelines, facilitating smooth communication and regulatory approval.
Germany – Precision and Compliance
Germany remains a global leader in pharmaceutical innovation and clinical trial operations. Our clinical trial translation services in Germany align with BfArM and Paul-Ehrlich-Institut (PEI) requirements. Prism guarantees accurate, high-quality translations tailored to German regulatory expectations.
France – Regulatory Expertise for ANSM and CPP
France’s clinical trials are strictly regulated by ANSM and Comités de Protection des Personnes (CPP). Prism Translation Services provides French clinical research translations that meet both local and EU submission standards, helping sponsors and CROs reduce delays and enhance clarity for ethics committees and trial participants.
Why Choose Prism Translation Services?
Native Medical Translators with clinical and scientific backgrounds
ISO 17100 & ISO 9001:2015 Certified Processes
Fast Turnaround and urgent delivery options
Confidential and GDPR-Compliant Handling of patient data
100% Regulatory Accuracy for EU, EMA, and FDA guidelines
Trusted by Global Clients
Prism works with:
Clinical Research Organizations (CROs)
Pharmaceutical and Biotech Companies
Academic Hospitals and Research Centers
Regulatory Affairs Consultants
Global Health Agencies
Expert Clinical Research Translation Services in Poland, Germany, France
Prism Translation Services offers expert Clinical Trials Translation Services in Poland, Germany, and France, ensuring complete linguistic accuracy and regulatory compliance. With increasing demand for multilingual documentation in the European clinical research sector, we specialize in translating essential materials such as informed consent forms (ICFs), clinical trial protocols, and ethics committee submissions. Our certified medical translators work with Polish, German, and French languages, guaranteeing high-quality results that align with EMA, BfArM, ANSM, and URPL requirements. Whether you are a pharmaceutical company, CRO, or research institution, our services help you streamline cross-border trials and accelerate approval processes.
With years of experience in the life sciences sector, Prism Translation Services is trusted by global clients for precise and confidential clinical research translation. We support all phases of clinical trials and provide fast, ISO 17100 & ISO 9001:2015 certified translations across Europe. Our GDPR-compliant workflows protect sensitive patient data while ensuring clear communication with regulatory authorities. If you are looking for clinical trial document translation in Germany, multilingual CRO support in Poland, or medical translation services in France, Prism is your reliable partner for success in international clinical research.