Built for accuracy, traceability, and clarity across the life sciences content lifecycle
Built for the AI era of life sciences translation
Next-Generation Life Sciences Translation for Regulated Global Content
Sesen helps clinical, regulatory, labeling, safety, medical device, and commercial teams manage multilingual content with SesenGPT-enabled workflows, expert human review, terminology governance, validation, and quality-controlled delivery.
EXPLORE SESENGPTLife Sciences Only
Specialized workflows for regulated clinical, regulatory, labeling, and safety content
SesenGPT-Enabled
AI-supported translation workflows designed for life sciences content
Human-Validated Quality
Expert human review remains central to accuracy, context, and final quality
AI Translation Validation
Structured QA supports terminology, completeness, consistency, and traceability
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.
Clinical Trial Translation Services
Informed consent forms, protocols, study documents, patient materials, and clinical communication for global trials.
Explore serviceRegulatory Submission Translation Services
Submission-ready multilingual support for regulatory dossiers, agency correspondence, and approval workflows.
Explore serviceDrug Labeling & Packaging Translation
Quality-controlled labeling translation for prescribing information, packaging, patient leaflets, and product updates.
Explore serviceIFU Translation Services
Instructions for use, device labeling, user manuals, safety information, and patient-facing device content.
Explore serviceClinical & Medical Software Localization
Software UI, eCOA, digital health, medical device software, and clinical platform localization with in-context review.
Explore serviceeLearning & Training Translation Services
Multilingual training, compliance learning, product education, voiceover, subtitles, and interactive course localization.
Explore serviceMarketing and Commercial Translation
Life sciences marketing, medical affairs, brand, launch, and post-market communication adapted for global audiences.
Explore serviceLife 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.
Biotechnology
Multilingual support for biologics, biosimilars, genomics, gene therapy, research communication, clinical development, and global market readiness.
Medical Devices
Specialized translation for IFUs, device labeling, software UI, risk information, training materials, and post-market communication.
CROs
Scalable language support for clinical study documentation, patient-facing materials, ethics submissions, investigator communication, and local reviewer coordination.
Healthcare & Hospitals
Translation and localization for patient education, EHR content, public health communication, clinical training, and multilingual care access.
Regulatory & Government
Language services for public health programs, policy documents, regulatory communication, submissions, compliance materials, and multilingual outreach.
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.
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.
Supporting resources
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.
1
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.
Explore solution2
Regulatory Submission Readiness
Translation workflows for regulatory dossiers, agency correspondence, approval documentation, compliance materials, and global submission timelines.
Explore solution3
Labeling Translation and Review
Controlled multilingual support for drug labeling, packaging, IFUs, safety updates, version control, and in-context label review.
Explore solution4
AI Translation Validation
Human-led validation for AI-translated content, including terminology, accuracy, completeness, formatting, consistency, and risk-focused QA.
Explore solution5
Terminology Governance
Glossaries, style guides, approved term management, translation memory leverage, and terminology intelligence across products and markets.
Explore solution6
Multilingual Software and eCOA Localization
Localization for clinical platforms, eCOA, medical software, digital health products, UI strings, screenshots, and in-context review workflows.
Explore solution7
Global Linguistic Review Services
Expert review for client-generated, AI-translated, or locally adapted content before publication, submission, launch, or market use.
Explore solution8
Modular Submission & Content Reuse
Multilingual content reuse strategies for modular submissions, recurring updates, shared source content, terminology consistency, and version control.
Explore solutionTrusted 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.
Explore Clinical & Regulatory Knowledge Insights
View all resources
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.