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About Sesen

Built for Regulated Multilingual Life Sciences Communication

Sesen helps pharmaceutical, biotechnology, medical device, CRO, and healthcare organizations manage multilingual clinical, regulatory, labeling, and digital health content across 150+ languages through expert human linguists, controlled workflows, and AI-enabled translation technologies.

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Life Sciences Focused
150+ Languages
ISO 17100 / 9001 / 13485
Global Language Operations
Regulated multilingual workflows for life sciences
Secure Workflow
Clinical Translation
Study startup & patient-facing materials
Regulatory Content
Submission-ready multilingual workflows
AI-Enabled Workflow
Human expertise enhanced by structured AI-assisted operations
150+
Languages Supported
ISO
Certified Processes
AWS
Secure Infrastructure

Sesen at a Glance

Sesen supports pharmaceutical, biotechnology, medical device, CRO, and healthcare organizations with specialized multilingual solutions designed for regulated life sciences environments.

Specialization

Life Sciences Focused

Specialized exclusively in life sciences translation, localization, and multilingual content operations.

Global Scale

150+ Languages Supported

Global language support for clinical trials, regulatory submissions, product labeling, IFUs, and patient-facing materials.

Quality Systems

ISO-Certified Processes

ISO 17100, ISO 9001, and ISO 13485 certified workflows designed for regulated environments.

Human Expertise

Professional Native Medical Linguists

Experienced linguists with subject matter expertise in pharmaceuticals, biotechnology, medical devices, CROs, and healthcare.

Workflow Innovation

AI-Enabled Workflows With Human Review

Structured AI-assisted translation workflows combined with expert human review, terminology management, and multilingual QA.

Content Coverage

Clinical, Regulatory, and Software Localization Support

Support for clinical documentation, regulatory content, drug labeling, IFUs, eHealth platforms, medical software, and digital health applications.

Trusted by global life sciences organizations to support multilingual communication across research, regulatory, product, and patient engagement workflows.

Why Sesen Was Created

Life sciences organizations operate in one of the most regulated and globally interconnected industries in the world. Clinical trial materials, regulatory submissions, drug labeling, IFUs, patient communications, and digital health platforms must be translated accurately and consistently across languages, markets, and regulatory environments.

Traditional translation approaches were not designed for the operational and compliance requirements of modern life sciences organizations. Generic workflows often lack the subject matter expertise, terminology control, multilingual coordination, and structured review processes required for regulated content.

Sesen was created to address this need.

Established from CSOFT’s long-standing experience supporting global life sciences organizations and multilingual operations, Sesen was built specifically to support regulated multilingual communication across pharmaceutical, biotechnology, medical device, CRO, and healthcare environments.

Our approach combines professional native medical linguists, structured quality processes, terminology management, multilingual workflow coordination, and AI-enabled technologies to help organizations manage global content more efficiently while maintaining quality and operational control.

Enterprise Foundation

Built specifically for regulated life sciences communication

Specialized exclusively in life sciences translation and localization

Designed for regulated multilingual workflows

Structured terminology and quality management processes

AI-enabled workflows with expert human review

Global support across clinical, regulatory, labeling, and digital health content

Enterprise-focused operational model for multilingual life sciences communication

Regulated Content Operations

Built Around Regulated Life Sciences Content

Sesen supports multilingual workflows designed specifically for regulated life sciences communication, helping global organizations manage clinical, regulatory, labeling, software, and patient-facing content with greater consistency, scalability, and operational control.

Sesen’s operational model combines domain expertise, terminology management, multilingual coordination, controlled review workflows, global rollout support, and AI-enabled technologies to support scalable, regulatory-ready communication for life sciences organizations.

AI-Assisted Multilingual Operations

Human Expertise Enhanced by AI-Enabled Workflows

Sesen combines professional native medical linguists, structured quality processes, and AI-enabled technologies to support scalable multilingual communication for regulated life sciences environments. AI supports efficiency and consistency, while expert human review remains central to the workflow.

Controlled Multilingual Workflow

AI-enabled support within a human-led review process

Designed for regulated content
01

Source Content Intake

Clinical, regulatory, labeling, software, and patient-facing content is prepared for multilingual workflow management.

02

AI-Assisted Translation

AI-enabled technologies support translation efficiency, content reuse, and multilingual processing within a controlled workflow.

03

Terminology Validation

Approved terminology, product naming, medical concepts, and regulatory language are checked for consistency across markets.

04

Human Medical Review

Professional native medical linguists review content for accuracy, context, clarity, and life sciences subject matter quality.

05

QA & Consistency Checks

Automated and human QA processes support checks for terminology, numbers, formatting, structure, and multilingual consistency.

06

Final Controlled Output

Final multilingual content is delivered through structured workflows designed for regulatory-ready communication.

Translation Memory

Supports content reuse and consistency across recurring clinical, regulatory, labeling, and software content.

Terminology Management

Aligns approved medical terminology, product names, regulatory language, and multilingual content standards.

QA Automation

Supports checks for terminology, numbers, formatting, repeated content, and multilingual content structure.

AI-Assisted Translation

Helps accelerate multilingual workflows while remaining connected to expert human review and quality controls.

Human Review

Keeps professional native medical linguists central to clinical, regulatory, safety, and patient-facing content workflows.

Side-by-Side Validation

Supports comparison, review, change tracking, and collaborative validation across multilingual teams.

Workflow Traceability

Provides structured workflow management, version control, review visibility, and operational accountability.

SesenGPT

Purpose-built AI support for life sciences translation workflows

SesenGPT supports AI-enabled multilingual workflows designed specifically for regulated life sciences communication, helping teams improve terminology consistency, multilingual efficiency, and workflow coordination without removing expert human oversight.

Terminology consistency Human review Workflow visibility Regulated content support

Sesen’s approach combines expert human linguists, controlled review workflows, terminology management, multilingual coordination, and AI-enabled technologies to help life sciences organizations manage global communication with greater consistency, scalability, and operational confidence.

Global Operations & Multilingual Scale

Supporting Global Life Sciences Teams Across Markets

Sesen supports global life sciences organizations through centralized multilingual program management, regional linguistic expertise, structured workflow coordination, and scalable localization operations designed for regulated communication environments.

Global Multilingual Infrastructure
Operational support across regulated international markets
150+ Languages
Americas Europe Asia-Pacific Global rollout
150+ Languages
Global Multilingual Support
Centralized Workflow Coordination
Regional Linguistic Expertise
01

Global Multilingual Program Coordination

Sesen supports multilingual clinical, regulatory, labeling, software, and patient engagement programs through centralized operational oversight and coordinated global workflows.

Cross-market coordination Centralized communication Scalable multilingual execution
02

Regional Linguistic Expertise

Professional native medical linguists support regional terminology alignment, localization adaptation, and country-specific linguistic review across regulated markets.

Regional terminology support Country-specific review Healthcare system awareness
03

Global Rollout Support

Operational workflows are designed to support synchronized multilingual launches across clinical, regulatory, labeling, software, and patient communication environments.

Launch coordination Workflow visibility Cross-market consistency
04

Centralized Localization Operations

Sesen combines centralized program management, terminology systems, multilingual review workflows, and operational visibility to support scalable global communication.

Terminology management Version control Structured review workflows
Sesen supports global life sciences organizations through scalable multilingual operations designed to help teams manage clinical, regulatory, labeling, software, and patient-facing communication more consistently across international markets and regulated environments.
Quality, Compliance, and Security

Quality Systems Designed for Regulated Environments

Sesen’s operational framework combines structured quality processes, terminology management, multilingual workflow controls, professional human expertise, and secure infrastructure to support regulated life sciences communication across global markets.

Quality Infrastructure

ISO-Certified Quality Processes

Structured quality management frameworks designed to support regulated multilingual workflows across life sciences environments.

ISO 17100
ISO 9001
ISO 13485
Workflow Governance

Workflow Controls and Audit Readiness

Operational workflows support multilingual coordination, review traceability, version management, and structured oversight.

Review traceability
Version control
Audit support
Linguistic Operations

Linguistic QA and Review Workflows

Professional medical linguists and structured QA processes support multilingual consistency across regulated content environments.

Terminology checks
Formatting verification
Controlled review workflows
Terminology Governance

Terminology Management and Consistency Control

Centralized terminology systems help maintain multilingual consistency across clinical, regulatory, labeling, and software content.

Translation memory
Regulatory terminology alignment
Cross-market consistency
Secure Infrastructure

AWS-Hosted Operational Environment

Controlled infrastructure and operational access management designed to support enterprise life sciences communication workflows.

AWS-hosted systems
Controlled user access
Secure file management
Confidentiality Support

Confidentiality and Regulated Communication

Operational workflows support confidentiality-focused multilingual coordination across clinical, scientific, and regulatory environments.

Restricted access processes
Controlled content handling
Enterprise communication support
Sesen’s quality, compliance, and operational framework is designed to support multilingual communication through structured workflows, terminology consistency, controlled review processes, secure infrastructure, and scalable operational support for regulated global environments.
Operational Partnership

How We Work With Clients

Sesen works closely with pharmaceutical, biotechnology, medical device, CRO, and healthcare organizations to support multilingual communication through structured workflows designed for regulated global environments.

Collaborative Operational Model

Structured multilingual collaboration designed for regulated environments

Program Management Linguistic Expertise Workflow Coordination QA Oversight Global Rollout Regulatory Support Client Collaboration

Effective multilingual programs require operational consistency, terminology alignment, and close collaboration across global teams.

01

Long-Term Multilingual Partnership

Sesen supports ongoing multilingual initiatives across clinical development, regulatory affairs, labeling, software localization, and global product communication through workflows designed for continuity, terminology alignment, and scalable collaboration.

02

Responsiveness and Operational Coordination

Structured project management, centralized communication workflows, and multilingual operational coordination help support evolving timelines and global regulatory requirements.

03

Scientific and Linguistic Precision

Professional native medical linguists, terminology management systems, structured review workflows, and AI-enabled QA support help maintain multilingual consistency across regulated content environments.

04

Transparency and Workflow Visibility

Sesen’s operational model emphasizes collaborative review support, workflow transparency, version visibility, and structured multilingual coordination across distributed teams.

05

Scalable Global Support

Scalable operational workflows support multilingual communication across expanding products, studies, regulatory programs, software platforms, and patient engagement initiatives.

Sesen’s approach combines operational coordination, scientific and linguistic expertise, structured workflows, multilingual scalability, and collaborative client support to help life sciences organizations manage regulated global communication across evolving international environments.

Looking Ahead

The Future of Regulated Multilingual Communication

Sesen continues to invest in multilingual workflow innovation designed to help life sciences organizations manage increasing global communication complexity through scalable, structured, and operationally coordinated environments.

Global Content
AI-Enabled Multilingual Operations
Structured workflow infrastructure designed to support regulated life sciences communication at global scale.
Regulatory-Ready Communication

Through initiatives such as SesenGPT, Sesen continues to expand AI-enabled multilingual workflow capabilities designed to support terminology consistency, workflow visibility, operational scalability, and structured global communication for regulated life sciences environments.

Sesen continues to invest in multilingual workflow innovation, operational scalability, and AI-enabled technologies designed to help life sciences organizations manage regulated global communication with greater consistency, efficiency, and long-term operational confidence.

Global Life Sciences Communication

Talk With Team Sesen

Discuss your clinical, regulatory, labeling, software localization, or multilingual workflow requirements with Sesen’s life sciences localization specialists.

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150+ Languages
ISO-Certified Workflows
AI-Enabled Operations
Regulated Content Support