Pharmaceutical companies trust XTM to handle their most critical translation projects. From drug labeling to clinical trials, our platform delivers the accuracy, security, and compliance features your regulatory team needs to succeed globally.
Transform your global reach with translation technology built specifically for life sciences compliance and quality standards.
supported languages
words translated per year
global customers
Complex regulatory requirements create translation bottlenecks that delay product launches. Medical terminology inconsistencies risk patient safety and regulatory rejection.
XTM eliminates these risks with purpose-built pharma translation workflows. Our platform ensures every document meets FDA, EMA, and international compliance standards while maintaining medical accuracy.
Built specifically for pharmaceutical companies, XTM streamlines your most complex translation challenges while maintaining the highest quality and compliance standards.
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
Every feature addresses the unique challenges pharmaceutical companies face when translating critical documents for global markets.
Centralized control ensures medical terms stay consistent across all translations, reducing regulatory risk and maintaining patient safety standards.
Complete change tracking meets FDA and EMA requirements, providing the documentation needed for successful regulatory submissions and inspections.
Automated checks catch errors in medical terminology, formatting, and compliance requirements before documents reach regulatory authorities or patients.
Streamlined workflows connect medical writers, translators, and reviewers in one platform, reducing review cycles and accelerating approval processes.
Direct integrations with CCMS, regulatory systems, and content management platforms eliminate manual file transfers and reduce processing time.
Enterprise-grade security protects sensitive pharmaceutical data while maintaining compliance with international privacy and regulatory standards.
XTM connects directly with regulatory databases, content management systems, and platforms your team already uses.
Our platform provides complete audit trails, terminology management, and quality assurance features that meet FDA, EMA, and international regulatory requirements. Every change gets tracked automatically, creating the documentation needed for successful regulatory submissions.
You can demonstrate compliance with detailed reports showing who made changes, when they occurred, and what approvals were obtained throughout the translation process.
XTM was built specifically for industries requiring strict compliance and quality control. Our terminology management prevents dangerous inconsistencies in medical terms, while our audit trails meet pharmaceutical regulatory standards.
General translation platforms lack the specialized features pharmaceutical companies need for regulatory submissions, clinical trials, and patient safety documentation.
Yes, our platform processes billions of words annually for enterprise customers. Whether you’re translating thousands of drug labels or managing complex clinical trial documentation across multiple languages, XTM scales to meet your volume requirements.
Our infrastructure supports simultaneous translation projects without compromising quality or compliance standards.
Our centralized terminology database ensures medical terms, drug names, and safety information remain consistent across all languages. You can create controlled vocabularies, set approval workflows, and prevent unauthorized term changes.
This reduces regulatory risk and protects patient safety by maintaining accuracy in critical pharmaceutical communications across global markets.
XTM maintains SOC 2 Type II, ISO 27001, and GDPR compliance. Our enterprise-grade security includes data encryption, access controls, and monitoring systems designed for sensitive pharmaceutical content.
Your clinical data, regulatory submissions, and patient information stay protected while meeting international privacy and security requirements.
Most pharmaceutical teams start translating within days of setup. Our implementation specialists understand pharmaceutical workflows and can configure terminology databases, compliance settings, and user permissions quickly.
We provide dedicated support during onboarding to ensure your team can immediately begin managing pharma translation projects with full compliance features.
Yes, our connector ecosystem includes direct integrations with CCMS platforms, regulatory databases, and content management systems. These connections eliminate manual file transfers and reduce processing time for pharmaceutical translation projects.
Your existing workflows remain intact while gaining access to specialized pharma translation features and compliance capabilities.
Our platform manages all pharmaceutical content types, including drug labels, patient leaflets, clinical protocols, regulatory submissions, and medical device documentation. Each document type can have customized workflows, terminology controls, and quality assurance checks.
From small patient information updates to large-scale global product launches, XTM handles the full range of pharmaceutical translation requirements.
Dig deeper into how XTM delivers faster localization, greater control, and real ROI—so you can make the right call for your team.
