Simplify global compliance for life sciences. Smartcat's AI platform streamlines your regulatory document translation workflow. Translate clinical trial documents, manage biotechnology quality control document translation, and handle other sensitive materials with confidence, all on a single, secure platform.
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Thousands of global companies, including life sciences leaders, trust Smartcat for secure, AI-powered regulatory document translation.
95%+
AI Quality for Compliance
Achieve high accuracy for your medical regulatory documents translation with expert-enabled AI that learns from your edits.
2x
Faster Global Submissions
Reduce turnaround times by creating and translating documents simultaneously, not sequentially.
50%
Lower Translation Costs
Translate more content for your budget by leveraging AI and reusing approved translations.
From clinical research to post-market surveillance, our platform handles a wide range of technical and regulatory documentation translation needs.
Clinical Trial Documentation
Informed Consent Forms (ICFs)
Package Inserts & Labels
Manufacturing Procedures
Biotechnology Quality Control
Automated Workflows
Centralized Collaboration
Consistent Quality
Expert Review
for platform setup simplicity
for ease of platform use
global clients, including life sciences
of Fortune 500 customers
5 Steps for Compliant Document Translation
1
Upload Your Documents in Any Format
2
Select Your Target Languages
3
Let AI Agents Translate Your Content
4
Invite Subject-Matter Experts to Review
5
Download Your Compliant Translated Documents
400%
Faster Translation Turnaround
Achieved by Smith+Nephew after switching to Smartcat.
70%
Significant Cost Savings
For Stanley Black & Decker, increasing quality and efficiency.
31 hours
Work Hours Saved Monthly
For Babbel’s marketing and L&D teams.
Streamline your workflow with Smartcat's AI platform. Achieve high translation quality for your technical and regulatory documentation translation, while reducing costs and accelerating time-to-market.
We handle a wide range of documents, including clinical trial protocols, informed consent forms (ICFs), biotechnology quality control document translation, manufacturing guides, package inserts, and more. Our platform supports the full scope of medical regulatory documents translation.
Smartcat uses multiple layers of quality control. Our AI is trained on industry-specific data. You can upload glossaries to enforce correct terminology, and translation memory reuses previously approved translations. Finally, you can hire subject-matter expert reviewers from our marketplace.
Smartcat is SOC 2 Type II compliant and provides a secure environment for your sensitive data with end-to-end encryption and granular access controls. This ensures your regulatory document translation process is secure from start to finish.
Yes. Smartcat offers unlimited seats at no extra cost. You can invite your internal team, in-country reviewers, or external partners to collaborate on the platform, ensuring everyone works from a single source of truth.
Smartcat is an AI platform that unifies your entire content lifecycle. Instead of a slow, sequential process, you can create and translate content simultaneously. This eliminates manual handoffs, reduces costs, and significantly speeds up your time-to-market for global launches.
Our AI Agents are more than just machine translation. They are expert-enabled, meaning they continuously learn from your edits, glossaries, and translation memories. This creates a feedback loop that improves accuracy and consistency with every project.
Yes, Smartcat is designed to handle complex document formats common in life sciences. The platform works to preserve your original layout, tables, and figures, reducing the need for extensive reformatting after translation.
We prioritize your data's security. Smartcat is SOC 2 Type II compliant and features end-to-end encryption. Your data is not used to train public AI models, and you have full control over who can access your projects.