In the pharmaceutical industry, translation errors can lead to delays, compliance risks, or safety concerns. With tight deadlines and growing multilingual demands, accuracy is essential. DeepL's Language AI delivers secure, accurate, and compliant translations you can rely on. Start translating with confidence
Regulatory agencies like the FDA and EMA require strict consistency and flawless terminology in pharmaceutical documents. A single translation error can cause delays, failed audits, or legal risk. DeepL’s AI-driven solution helps teams maintain accuracy, reduce review time, and ensure compliance with the most demanding regulatory standards.
In pharma, even small translation errors can lead to safety risks or regulatory issues. Scientific content requires precise terminology and deep industry knowledge. DeepL ensures that complex language is accurately preserved and aligned with regulatory expectations.
Pharma teams must manage multilingual content across clinical, regulatory, and commercial workflows. This requires flawless coordination and strict quality control. DeepL helps ensure consistency and compliance throughout the process, reducing risk and time.
Pharma translation involves highly sensitive data that must be protected at all times. DeepL uses enterprise-grade security, encryption, and audit trails to ensure full compliance and maintain patient and regulatory trust from start to finish.
Pharmaceutical translation needs a partner that understands the stakes. Our platform stands out with purpose-built features that help you navigate the complexity of pharma communications with confidence.
DeepL Translator enables you to translate entire documents like clinical protocols, regulatory dossiers, and patient materials in seconds, while preserving formatting and structure. This streamlines review cycles, ensures consistency, and helps teams stay compliant with tight regulatory timelines.
DeepL’s glossary lets you define approved translations for complex medical terms across more than 30 languages. Maintain accuracy and consistency in trial materials, regulatory documents, and patient-facing content.
DeepL API connects directly to your content or regulatory systems, automating translations across clinical trials, submissions, and packaging. This reduces manual work, speeds up processes, and ensures accuracy across multilingual workflows.
DeepL helps pharmaceutical companies manage multilingual content from early research to global launch. Our solutions are tailored to meet complex regulatory, clinical, and commercial translation needs at every stage of the product lifecycle.
DeepL enables clinical, legal, and regional teams to collaborate in real time with in-line commenting and tagging. Feedback is tracked, validated translations are preserved, and all changes are fully traceable, helping your teams meet global compliance standards without delays.
DeepL translates entire regulatory documents into multiple languages while preserving formatting, eliminating the need for manual copy-paste. This allows your teams to stay on schedule while meeting regulatory expectations in every language.
DeepL’s enterprise Language AI meets the highest global standards for data protection, with certifications including ISO 27001, SOC 2 Type II, BSI C5 Type 2, HIPAA, and GDPR. Features such as Bring-Your-Own-Key (BYOK) encryption, SSO, multi-factor authentication (MFA), and audit logs ensure full control, transparency, and compliance across your pharma translation workflows.
DeepL powers translations for over 200,000 organizations with unmatched speed and quality. Built on proprietary language data and human guidance, it handles complex scientific terminology in over 30 languages, helping pharma teams meet deadlines while staying compliant and consistent.
Yes. DeepL Language AI meets enterprise-grade security standards with ISO 27001, SOC 2 Type II, HIPAA, and GDPR certifications. Your clinical data is never used to train DeepL’s models, ensuring complete confidentiality.