Global Life Sciences Translation, Enhanced by AI

Sesen specializes exclusively in life sciences translation, combining expert human linguists, regulatory-focused workflows, and AI-enabled language technology to help pharmaceutical, biotech, CRO, and medical device companies translate with greater speed, consistency, and confidence.

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Trusted by global life sciences teams for clinical, regulatory, and product content across 150+ languages.

SesenGPT Workflow

AI + Human Translation Control

Content Analysis

Clinical, regulatory, product, and patient-facing content prepared for multilingual workflows.

AI-Enabled Processing

Translation memory, terminology intelligence, and selective AI support improve speed and reuse.

Expert Human Review

Professional life sciences linguists review content for accuracy, clarity, and regulated use.

150+

Languages supported for global programs

ISO

Quality-focused workflows for regulation

AI + Human

Technology-enabled expert review

Life Sciences

Clinical, regulatory, and patient content

AI-Enabled Translation for Regulated Life Sciences Content

Sesen brings together professional life sciences linguists, structured translation workflows, terminology management, and SesenGPT-powered technology to support faster and more consistent translation across global programs. Our approach is designed for real-world regulated content workflows, where accuracy, traceability, and clarity matter as much as speed.

We support

Clinical trial translation, including informed consent forms and patient-facing materials
Regulatory submissions and global dossier updates
Drug labeling and packaging translation lifecycle
Medical device IFU and product documentation
Post-approval content updates and localization

Why Sesen works for regulated translation

Human expertise with domain-specific life sciences knowledge
AI-assisted workflows for speed and consistency, not risk
Built-in QA checks for terminology, numbers, and formatting
Translation memory reuse for ongoing programs
Designed for regulated environments and global rollout

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Life Sciences Translation Services for Regulated Content

Sesen provides specialized translation services for clinical, regulatory, medical device, and life sciences software content, combining professional domain expertise with AI-enabled workflows and expert human review. Our approach supports consistent, accurate, and scalable multilingual communication across global programs, while maintaining the quality and control required for regulated environments.

Clinical Trial Translation

Translation for informed consent forms, clinical study documents, patient-facing materials, eCOA/ePRO, and global site communications.

→ View Clinical Trial Translation Services

Regulatory & Labeling Translation

Translation support for regulatory submissions, drug labeling, packaging content, and country-specific documentation requirements.

→ View Regulatory Translation Services

Medical Device Translation

Translation of IFUs, product labeling, user manuals, safety documentation, and technical content for global device markets.

→ View Medical Device Translation Services

Clinical & Medical Software Localization

Localization of eClinical platforms, medical applications, and software UI content with in-context review and linguistic validation.

→ View Software Localization Services

eLearning & Training Localization

Localization of training modules, eLearning courses, and instructional content for global teams and life sciences professionals.

→ View eLearning Localization Services

Industry Expertise Across Life Sciences

Sesen supports pharmaceutical, biotechnology, medical device, CRO, and healthcare organizations with specialized translation for regulated content across global markets.

Our teams understand the terminology, workflows, and compliance requirements associated with clinical trials, regulatory submissions, product labeling, and patient-facing materials.

The Sesen Advantage

Sesen combines life sciences expertise with structured workflows and AI-enabled technology to support high-quality, scalable translation for regulated environments.

Driven by Quality, Committed to Compliance.

Our rigorous workflows and certifications ensure your translations meet global standards.

ISO 17100

Defines requirements for professional translation services, ensuring a consistent and reliable delivery process.

ISO 9001

A universal standard for quality management systems, reflecting our commitment to continuous improvement.

ISO 13485

Specifically tailored to medical devices, guaranteeing safe and effective product documentation.

HIPAA & GDPR

Protecting sensitive data and safeguarding patient privacy across borders.

We start by selecting linguists with specialized medical or scientific backgrounds, then apply multiple revision cycles to ensure accuracy and clarity. Alongside client-specific glossaries and CAT tools, this approach maintains consistency and reduces errors. Finally, every translation undergoes a thorough compliance check, meeting strict regulatory standards before delivery.

All file exchanges utilize encrypted channels and secure servers, safeguarding sensitive life sciences data. We require strict NDAs from every team member, ensuring confidentiality of patient information, clinical research, and proprietary content. By adhering to both HIPAA and GDPR, we maintain high privacy standards that protect global stakeholders’ trust.

Our project management system logs each stage of the translation process, providing full traceability for regulatory bodies. Established SOPs and certified workflows enable quick and efficient responses during inspections. Continuous improvement practices further enhance quality, helping us consistently meet or exceed industry expectations.

Why Life Sciences Teams Choose Sesen

Sesen supports global life sciences organizations with translation solutions designed for regulated content, combining domain expertise, structured workflows, and AI-enabled technology with expert human review.