Next-Generation Life Sciences Translation Services

Professional Translation for Regulated Global Content, Enhanced by AI

Sesen helps pharmaceutical, biotech, medical device, CRO, and healthcare teams translate clinical, regulatory, labeling, safety, software, training, and commercial content through expert linguists, AI-enabled workflows, terminology governance, and validation.

What Sesen Does

Specialized Translation and Localization for Life Sciences Organizations

Sesen supports regulated multilingual content across the life sciences product lifecycle, from clinical development and regulatory submission to labeling, safety, training, medical affairs, commercialization, and post-market communication.

Our work combines SesenGPT-enabled workflows, professional native translators, subject-matter review, terminology governance, translation memory leverage, AI-assisted validation, and structured quality checks for content where accuracy, consistency, and accountability matter.

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Clinical Trial Translation Services

Informed consent forms, protocols, study documents, patient materials, and clinical communication for global trials.

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Regulatory Submission Translation Services

Submission-ready multilingual support for regulatory dossiers, agency correspondence, and approval workflows.

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Drug Labeling & Packaging Translation

Quality-controlled labeling translation for prescribing information, packaging, patient leaflets, and product updates.

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IFU Translation Services

Instructions for use, device labeling, user manuals, safety information, and patient-facing device content.

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Clinical & Medical Software Localization

Software UI, eCOA, digital health, medical device software, and clinical platform localization with in-context review.

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eLearning & Training Translation Services

Multilingual training, compliance learning, product education, voiceover, subtitles, and interactive course localization.

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Marketing and Commercial Translation

Life sciences marketing, medical affairs, brand, launch, and post-market communication adapted for global audiences.

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Life Sciences Sectors

Serving Life Sciences Organizations Advancing Global Health

Sesen supports the specialized language needs of life sciences organizations working across research, development, regulatory approval, product launch, patient communication, and post-market operations, with AI-enabled workflows designed for speed, consistency, and expert human validation.

Pharmaceuticals

Translation and localization for drug development, regulatory submissions, labeling, pharmacovigilance, medical affairs, training, and commercialization.

Clinical trial contentRegulatory dossiersDrug labeling

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Biotechnology

Multilingual support for biologics, biosimilars, genomics, gene therapy, research communication, clinical development, and global market readiness.

Biopharma contentGene therapyScientific materials

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Medical Devices

Specialized translation for IFUs, device labeling, software UI, risk information, training materials, and post-market communication.

IFU translationDevice softwareLabeling review

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CROs

Scalable language support for clinical study documentation, patient-facing materials, ethics submissions, investigator communication, and local reviewer coordination.

Study startupICF translationSite materials

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Healthcare & Hospitals

Translation and localization for patient education, EHR content, public health communication, clinical training, and multilingual care access.

Patient educationEHR contentClinical training

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Regulatory & Government

Language services for public health programs, policy documents, regulatory communication, submissions, compliance materials, and multilingual outreach.

Public healthPolicy documentsCompliance content

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Responsible AI-Enabled Workflows

AI-Enabled, Human-Validated Translation for Regulated Content

Sesen is built for the AI era of regulated multilingual content. Our SesenGPT-enabled workflows help life sciences teams move faster while keeping expert human review, terminology governance, validation, and quality-controlled delivery at the center of the translation process.

This approach is designed for clinical, regulatory, labeling, safety, medical device, software, training, and commercial content where speed matters, but accuracy, traceability, clarity, and human accountability remain essential.

Built for accuracy, traceability, and clarity

Sesen’s AI-enabled, human-validated workflow supports regulated content where translated terms, version updates, reviewer input, and quality checks may matter. By combining terminology governance, SesenGPT-assisted drafting, expert human review, and structured validation, Sesen helps life sciences teams improve multilingual consistency while maintaining human accountability.

EXPLORE SESENGPT AI TRANSLATION VALIDATION

Controlled workflow

From SesenGPT-assisted drafting to final human validation

Translation Memory and Terminology Governance

Approved terminology, style guidance, prior translations, and content rules are prepared before translation begins.

SesenGPT-Assisted Draft Translation

For suitable content, SesenGPT supports controlled draft translation within life sciences-trained language workflows.

Expert Human Editing and Review

Professional native translators and subject-matter reviewers refine content for accuracy, context, tone, terminology, and intended use.

AI-Assisted Validation and Quality Checks

Structured QA helps check terminology, numbers, completeness, formatting, consistency, and potential multilingual risk areas.

Final Human Validation and Delivery

Final review confirms translation quality, client instructions, formatting expectations, and delivery readiness.

Quality, Compliance, and Security

Quality-Controlled Workflows for Regulated Multilingual Content

Enterprise life sciences translation in the AI era requires more than linguistic accuracy. Sesen supports regulated multilingual programs with ISO-certified quality processes, SesenGPT-enabled workflows, professional native translators, subject-matter review, terminology governance, version control, audit-ready documentation, and secure workflow management.

ISO-Certified Quality Processes

Translation workflows supported by ISO 17100, ISO 9001, and ISO 13485 quality practices for regulated multilingual content.

Professional Native Translators and Reviewers

Life sciences linguists and subject-matter reviewers support clinical, regulatory, labeling, medical device, and safety content.

Terminology and Translation Memory Governance

Approved terms, style rules, and translation memory are managed to improve consistency across products, markets, and document versions.

Version Control and Reviewer Coordination

Structured workflows support content updates, local reviewer input, delta translation, and multilingual change management.

Audit-Ready Project Documentation

Project records can support traceability across source files, language scope, review steps, QA checks, delivery versions, and approvals.

Secure, Controlled Workflows Hosted on AWS

Sesen uses controlled translation workflows and AWS-hosted systems to support secure enterprise multilingual operations.

Quality Systems for Regulated Multilingual Programs

Sesen combines ISO-certified quality processes, terminology governance, reviewer coordination, AI-assisted validation, and controlled technology workflows to help life sciences teams manage multilingual content with transparency, consistency, and confidence.

QUALITY, COMPLIANCE & SECURITY CLIENT SUPPORT

Supporting resources

Certificate of Translation Accuracy Knowledge Base

AI-Enabled Enterprise Solutions

Solutions for Complex Life Sciences Translation Programs

Sesen helps enterprise life sciences teams manage multilingual content as a coordinated AI-enabled program, not a series of disconnected translation requests. Our solutions connect clinical, regulatory, labeling, software, AI translation validation, terminology intelligence, and expert human review workflows across teams, markets, and content lifecycles.

Clinical Trial Translation Programs

End-to-end support for study startup, informed consent forms, patient-facing materials, ethics submissions, study updates, and multilingual site communication.

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Regulatory Submission Readiness

Translation workflows for regulatory dossiers, agency correspondence, approval documentation, compliance materials, and global submission timelines.

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Labeling Translation and Review

Controlled multilingual support for drug labeling, packaging, IFUs, safety updates, version control, and in-context label review.

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AI Translation Validation

Human-led validation for AI-translated content, including terminology, accuracy, completeness, formatting, consistency, and risk-focused QA.

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Terminology Governance

Glossaries, style guides, approved term management, translation memory leverage, and terminology intelligence across products and markets.

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Multilingual Software and eCOA Localization

Localization for clinical platforms, eCOA, medical software, digital health products, UI strings, screenshots, and in-context review workflows.

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Global Linguistic Review Services

Expert review for client-generated, AI-translated, or locally adapted content before publication, submission, launch, or market use.

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Modular Submission & Content Reuse

Multilingual content reuse strategies for modular submissions, recurring updates, shared source content, terminology consistency, and version control.

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Connect SesenGPT, expert review, quality, and multilingual operations into one translation program

Explore Sesen solutions for teams managing high-volume, regulated, recurring, or multi-stakeholder life sciences content with AI-enabled workflows and human-validated delivery.

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Trusted by Leading Life Sciences Organizations

Representative clients across clinical, regulatory, medical device, and healthcare content programs.

Built for Enterprise Life Sciences Teams

Sesen gives enterprise clinical, regulatory, medical device, safety, training, and commercial teams a modern AI-enabled translation model built around SesenGPT, expert human validation, terminology governance, and quality-controlled multilingual delivery.

This model is designed for the next generation of life sciences translation, where AI accelerates suitable workflows while professional native translators, subject-matter reviewers, ISO-certified processes, and structured validation support accuracy, traceability, clarity, and human accountability.

SesenGPT

AI-enabled workflows for regulated life sciences content

ISO

17100, 9001, and 13485 quality foundation

150

Languages supported for global programs

AI-Native

Built around SesenGPT, human validation, and regulated workflows

AI-Enabled Program Support

SesenGPT-enabled workflows designed for suitable clinical, regulatory, labeling, safety, software, training, and commercial content

Expert human review and subject-matter oversight remain central to accuracy, context, and final delivery

AI-assisted validation supports terminology, completeness, formatting, consistency, and multilingual quality checks

Terminology intelligence, style guides, and translation memory governance improve consistency across products and markets

Dedicated project management coordinates reviewers, versions, timelines, and recurring multilingual content programs

AI-native operating model built around SesenGPT, human validation, regulated workflows, and enterprise-scale multilingual program support

Insights for Global Life Sciences Content Teams

Explore practical resources for clinical, regulatory, labeling, medical device, healthcare, and commercial teams managing multilingual content in the AI era, including responsible AI workflows, terminology intelligence, human validation, localization strategy, and regulated content readiness.

Clinical & Regulatory Resource Hub

Clinical & Regulatory Knowledge Insights

Educational articles and perspectives for clinical, regulatory, labeling, medical device, and quality teams managing regulated multilingual content across global life sciences programs.

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AI & Regulatory Insights

Perspective articles on responsible AI, regulatory translation, validation, terminology, and multilingual quality for life sciences teams.

Knowledge Base

Helpful explanations of life sciences translation concepts, regulated content workflows, terminology, QA, and localization best practices.

Blog & Insights

Articles and updates for clinical, regulatory, medical device, healthcare, and commercial content teams managing multilingual programs.

White Papers & E-Books

Downloadable resources for enterprise buyers evaluating translation quality, AI-enabled workflows, labeling, validation, and localization strategy.

Case Studies & Success Stories

Representative examples of how Sesen supports complex multilingual content programs across regulated life sciences environments.

Glossaries & Style Guides

Resources for terminology alignment, style guide development, reviewer coordination, and consistent multilingual content governance.

Work With an AI-Enabled Life Sciences Translation Partner

Sesen helps life sciences organizations manage multilingual clinical, regulatory, labeling, safety, software, training, and commercial content with SesenGPT-enabled workflows, expert human validation, terminology governance, and quality-controlled delivery.

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