AI Designed for Life Sciences
SesenGPT brings life sciences-adapted AI into controlled workflows, supported by customer terminology, approved content, and expert oversight.
LIFE SCIENCES FOCUSED
Clinical, regulatory & medical content
150+ LANGUAGES
Multilingual program support
GLOBAL OPERATIONS
Built on CSOFT experience
CONTROLLED QUALITY
Professional review & validation
Life Sciences Translation Expertise Backed by Global Operations
Sesen is the dedicated life sciences translation division of CSOFT International. We combine an established enterprise localization foundation with specialized clinical, regulatory, and medical language expertise.
Our teams support projects ranging from individual regulatory or clinical documents to coordinated multilingual programs across products, markets, and recurring updates.
About Sesen and CSOFTTrusted by Leading Life Sciences Organizations
Experience supporting complex clinical, regulatory, medical device, and healthcare communication programs.
How Sesen Improves Life Sciences Translation Programs
Life sciences organizations face growing volumes of multilingual content, tighter timelines, and pressure to improve efficiency without losing control over quality. Sesen connects specialized AI, professional expertise, and coordinated workflows to meet these challenges.
Human Expertise Where It Matters
Specialized medical linguists and qualified reviewers help preserve scientific meaning, clinical context, and regulatory terminology.
Better Translation Economics
AI assistance, translation memory, and approved content reuse help reduce repetitive effort and create opportunities for more efficient delivery.
Greater Control Across Markets
Coordinated project management, terminology governance, and structured review help teams manage complex multilingual programs.
Translation Services Across the Life Sciences Product Lifecycle
From early research and clinical development to regulatory approval, commercialization, and post-market operations, Sesen supports the content that life sciences organizations rely on to communicate globally.
Clinical Trial Translation
Support multinational studies with translation for protocols, informed consent forms, investigator materials, patient communications, and study updates.
Regulatory Submission Translation
Prepare multilingual regulatory dossiers, agency correspondence, technical information, and country-specific submission content.
Drug Labeling & Safety
Maintain consistent prescribing information, packaging, patient leaflets, labeling updates, and pharmacovigilance materials across markets.
Medical Devices & Diagnostics
Translate IFUs, device labeling, technical documentation, diagnostic system content, user manuals, and product communications.
Digital Health & Medical Software
Localize clinical platforms, medical device interfaces, eCOA systems, patient portals, and connected healthcare technologies.
Medical Affairs, Training & Commercial
Support global scientific exchange, HCP communications, medical education, product training, and commercial content.
Industries We Serve
Translation Expertise for Life Sciences Organizations
We tailor terminology, linguistic review, file handling, and delivery to the needs of pharmaceutical, biotechnology, medical device, CRO, healthcare, and public health teams.
Pharmaceuticals
Clinical development, regulatory submissions, drug labeling, safety, medical affairs, and commercialization.
Explore PharmaceuticalsBiotechnology
Biologics, biosimilars, cell and gene therapies, genomics, and emerging therapeutics.
Explore BiotechnologyMedical Devices & Diagnostics
IFUs, technical files, IVD documentation, software, product labeling, and training.
Explore Medical Devices & DiagnosticsContract Research Organizations
Clinical documentation, investigator communication, ethics submissions, and study operations.
Explore Contract Research OrganizationsHealthcare & Hospitals
Patient education, clinical information, digital health platforms, and care communication.
Explore Healthcare & HospitalsRegulatory & Public Health
Health authority communication, policy documentation, and multilingual public health information.
Explore Regulatory & Public HealthHow SesenGPT Combines AI Translation With Expert Review
Life sciences organizations can benefit from AI-assisted drafting and content reuse, but regulated materials still require scientific context, approved terminology, and accountable review.
SesenGPT combines life sciences-adapted AI, approved terminology, translation memory, specialized linguists, and structured validation. We configure each workflow to the content and its intended use, with qualified experts responsible for final quality decisions.
The SesenGPT workflow
A controlled approach from source to delivery
Prepare & Align
Source content, approved terminology, references, and project requirements.
Translate Intelligently
Controlled AI assistance and approved content reuse where suitable.
Review With Experts
Life sciences linguists evaluate accuracy, meaning, and context.
Validate Quality
Project-specific checks for completeness, numbers, and consistency.
Deliver & Improve
Complete final checks and maintain approved assets for future updates.
Professional Human Translation
Human-led translation and review for content requiring a primarily expert-driven approach.
SesenGPT-Assisted Translation
Controlled AI-enabled translation with professional editing, terminology, and quality validation.
Independent Translation Validation
Expert evaluation of existing or AI-generated translations against defined quality requirements.
Quality Controls for Regulated Life Sciences Translation
Life sciences translation requires more than linguistic fluency. Scientific accuracy, terminology consistency, patient understanding, document integrity, and controlled review all matter.
Our translation and review processes combine qualified professionals, terminology management, documented quality checks, controlled file handling, and project-specific requirements.
Specialized Linguistic Expertise
Medical, scientific, and technical linguists support accurate communication for specialized audiences.
Independent Review & Validation
Appropriate review steps help confirm source meaning, terminology, and project-specific requirements.
Terminology & Version Control
Approved glossaries, translation memory, and structured reviewer feedback maintain consistency.
Documented QA & Secure Handling
Quality checks, project documentation, and controlled file workflows support confidentiality and delivery readiness.
Case Studies, AI Insights, and Life Sciences Translation Resources
Explore life sciences translation program examples, practical guidance on AI-enabled workflows, and insights for clinical, regulatory, and medical device content teams.
CUSTOMER PROGRAMS
Life Sciences Translation Case Studies
Explore examples of multilingual translation programs covering clinical research, regulatory content, medical devices, and global communication.
Browse Case StudiesAI & REGULATORY
AI & Regulatory Translation Insights
Read practical perspectives on responsible AI, terminology governance, linguistic validation, and quality-controlled multilingual workflows.
Explore AI & Regulatory InsightsINDUSTRY PERSPECTIVES
Life Sciences Translation Articles
Discover articles on clinical translation, medical device localization, global content operations, and managing multilingual programs.
Explore Articles & InsightsDiscuss Your Life Sciences Translation Requirements
Whether you need support for a regulatory submission, clinical study, medical device update, or AI-assisted multilingual program, our team can help you plan the right workflow.
Share your content types, target languages, review requirements, and timelines. We'll recommend an approach appropriate to your project or ongoing translation program.
Life sciences specialization
AI-enabled workflows
Expert human review
Global language support