Secure pharmaceutical translation for global compliance
Streamline regulatory submissions, clinical trials, and drug labeling with XTM’s compliant translation management platform. Built specifically for pharmaceutical companies requiring audit trails, terminology control, and regulatory approval workflows.
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Trusted by global brands to power their localisation success
Achieve measurable results across global markets
Transform your pharmaceutical translation process with enterprise-grade tools designed for life sciences compliance. Reduce time-to-market while maintaining the accuracy and consistency required for regulatory approval.
880+
supported languages
18B+
words translated per year
1300+
global customers
Pharmaceutical translation challenges demand specialized solutions
Regulatory submissions, clinical trial documentation, and drug labeling require perfect accuracy across multiple languages. Traditional translation approaches create compliance risks and slow market entry.
XTM eliminates these bottlenecks with purpose-built pharmaceutical translation workflows. Our platform ensures consistency, maintains audit trails, and accelerates approval timelines while meeting strict regulatory requirements.
Accelerate market entry with compliant pharmaceutical translation
Purpose-built features ensure your pharmaceutical translation meets regulatory standards while reducing project timelines and operational overhead.
What our customers say
Deepak Nagabhushana
Staff Localization Project Manager, GoTo
Dominic Pemberton
VP of Content, RS Group
Alex Katsambas
Senior Head of Localization Services, FARFETCH
Vincent Rigal
CAT Tools Products Owner, Acolad
Comprehensive pharmaceutical translation features for every workflow
Essential tools designed specifically for pharmaceutical companies managing complex, regulated translation projects across global markets.
Centralized medical vocabulary control ensures consistent translation of critical terms across all languages, documents, and therapeutic areas while maintaining regulatory compliance standards.
Complete documentation of every change, approval, and revision creates compliance-ready records that satisfy FDA, EMA, and international regulatory body requirements.
Automated terminology checking, formatting validation, and compliance reviews catch errors before documents reach regulatory submission or patient distribution channels.
Streamlined workflows connect medical writers, translators, reviewers, and regulatory teams through role-based access controls and structured approval processes.
Direct integrations with content management systems, regulatory platforms, and clinical trial management tools eliminate manual file transfers and reduce project timelines.
Enterprise-grade security and unlimited project capacity support global pharmaceutical operations while maintaining data protection standards required for sensitive medical content.
60+ integrations to make your life easier
Seamlessly connect with existing regulatory systems, content management platforms, and clinical trial infrastructure for streamlined pharmaceutical translation processes.
Frequently asked questions
XTM maintains complete audit trails for every translation project, documenting changes, approvals, and reviewer actions. Our platform meets FDA, EMA, and international regulatory requirements through built-in compliance workflows.
Version control tracks every document revision with timestamps and user identification. Approval workflows ensure proper review sequences before final delivery.
Pharmaceutical translation requires specialized medical terminology, regulatory compliance documentation, and strict quality control processes. Standard translation tools lack the audit trails, terminology management, and compliance features needed for regulatory submissions.
XTM addresses these requirements with purpose-built pharmaceutical translation workflows. Our platform ensures consistency across therapeutic areas while maintaining the documentation needed for regulatory approval.
Yes, XTM processes billions of words annually for enterprise customers managing complex pharmaceutical translation portfolios. Our platform scales automatically to handle simultaneous projects across multiple therapeutic areas and regulatory regions.
Automated workflows distribute content efficiently while maintaining quality standards. Project managers can track progress across hundreds of documents simultaneously through centralized dashboards.
XTM’s terminology management centralizes medical vocabularies across all languages and therapeutic areas. Translators and reviewers access approved term databases that ensure consistency throughout every document and project.
Automated term checking flags inconsistencies during translation. Medical affairs teams can update terminology databases that immediately apply across all active projects.
XTM connects directly with regulatory submission platforms, clinical trial management systems, and content management tools used throughout the pharmaceutical industry. These integrations eliminate manual file transfers while maintaining compliance audit trails.
Popular integrations include regulatory platforms, clinical data management systems, and enterprise content repositories. Custom API connections support specialized pharmaceutical technology stacks.
Most pharmaceutical organizations complete XTM implementation within 30 days, including system integrations, terminology database setup, and user training. Our customer success team provides dedicated support throughout the entire onboarding process.
Implementation timelines depend on integration complexity and terminology database size. Standard deployments include workflow configuration, user training, and compliance validation testing.
XTM maintains SOC 2 Type II certification, ISO 27001 compliance, and GDPR adherence to protect sensitive pharmaceutical information throughout translation workflows. Our security infrastructure meets the highest standards required for regulated industries.
Data encryption, role-based access controls, and secure data centers protect intellectual property and patient information. Regular security audits validate our protection standards against evolving threats.
XTM offers flexible pricing models designed for pharmaceutical companies managing varying translation volumes throughout regulatory cycles. Enterprise plans include unlimited projects, users, and integration support with dedicated customer success management.
Pricing scales based on annual translation volume and feature requirements. Custom enterprise agreements support large pharmaceutical organizations with specific compliance or integration needs.
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