Services
Submissions, SOPs, audits, and regulated documentation.
ICFs, protocols, site documents, and patient materials.
COAs, PROs, patient questionnaires, and clinical instruments.
Medical, scientific, and technical life sciences content.
AE reports, DSURs, safety updates, and drug surveillance.
Regulated labeling and packaging for global product markets.
Instructions for Use translation for medical devices.
Device labeling for safety, compliance, and market access.
In-layout linguistic QA for packaging, IFUs, and labels.
Formatting and layout support for multilingual submissions.
Human-reviewed AI translation for regulated content.
Checks for terminology, numbers, formatting, and quality.
AI-assisted terminology extraction and consistency.
Routing, validation, terminology control, and human review.
Machine translation post-editing by medical linguists.
Clinical, medical, software, and digital health platforms.
Digital health apps, portals, and patient tools.
Video, training, voiceover, subtitling, and audiovisual content.
Multilingual voiceover and subtitles for training and communications.
Commercial, brand, and campaign translation for global markets.
Clinical, regulatory, labeling, safety, and commercialization support.
Research, genomics, gene therapy, biosimilars, and emerging therapeutics.
IFUs, labeling, software, technical documentation, and compliance content.
Clinical study operations, recruitment, site communication, and trial documents.
Patient-facing content, EHR documentation, telehealth, and care communication.
Health authority, public health, policy, and compliance-driven communication.
Public health programs, policy documents, and global health initiatives.
Digital health platforms, patient portals, eCOA, and clinical software.
Study startup, patient materials, clinical documentation, and global trials.
Submissions, labeling updates, safety documents, and compliance workflows.
Scientific exchange, publications, training, and medical communications.
Labeling, packaging, launch materials, updates, and commercialization.
Review clinical, regulatory, labeling, or AI-enabled workflow needs.
Structured multilingual workflows for regulated life sciences operations.
Multilingual support for global submissions, labeling, audits, and SOPs.
Translations for ICFs, protocols, site documents, and patient recruitment.
Specialized translations for AE/SAE reports, DSURs, and safety updates.
In-layout linguistic QA for packaging, IFUs, and labeling compliance.
Structured multilingual workflows for labeling translation, validation, and approval.
Component-based translation for IDMP, SPL, and XML content workflows.
Global communication and multilingual engagement programs.
Comprehensive support for launching products in international markets.
Culturally adapted outreach and multilingual trial communications.
Consistent scientific and brand language across markets.
Localized training for internal teams, HCPs, and external stakeholders.
Translation of websites, portals, and mobile health apps.
Sesen combines expert linguists, validation-driven review, and AI-assisted technologies to support global life sciences operations.
Proprietary AI, terminology, validation, and workflow systems for regulated multilingual content.
AI-assisted translation workflows built for regulated life sciences content.
Human-reviewed AI translation for quality, consistency, and scalability.
Automated checks for terminology, numbers, formatting, and compliance.
AI-assisted term extraction, harmonization, and reuse across global content.
Structured workflows for multilingual labeling translation, review, and validation.
AI-enabled workflows for clinical, regulatory, safety, and digital health teams.
AI-assisted multilingual support for ICFs, protocols, and patient materials.
Structured AI workflows for submissions, labeling, and compliance content.
AI-enabled workflows for AE reports, DSURs, safety updates, and drug surveillance.
AI-assisted localization for portals, apps, eCOA, and digital health platforms.
Coordinated multilingual workflows with AI routing and human review.
Start with a pilot that combines SesenGPT, professional native medical linguists, terminology control, and validation-driven QA.
Expert perspectives on AI, regulatory content, and multilingual life sciences communication.
Trends, analysis, and expert perspectives on multilingual life sciences communication.
Guidance on AI-enabled workflows, validation, terminology, and compliance.
Best practices for clinical trials, submissions, labeling, and global content operations.
Proof points, learning resources, and practical tools for multilingual content programs.
Examples of multilingual workflow support across life sciences organizations.
On-demand sessions and expert discussions on regulated multilingual operations.
Terminology resources for consistency across multilingual content programs.
Decision-support content for AI governance, quality, compliance, and translation strategy.
Detailed guidance on AI workflows, translation strategy, and global compliance.
Answers to operational, regulatory, and localization workflow questions.
Browse educational, technical, and customer-facing resources from Sesen.
Explore guidance on validation, terminology, structured content, and multilingual operations for life sciences organizations.
Mission, leadership, and values that guide Sesen’s life sciences localization work.
Regional footprint, partner ecosystem, and company updates across the industry.
A focused partner for high-stakes multilingual life sciences operations.
Sesen combines life sciences specialization, multilingual operations, and AI-enabled workflows for organizations that need quality, consistency, and scale.
Discuss enterprise translation, localization, or AI-enabled workflow needs.
Choose the right path for a new translation, localization, or AI-enabled workflow.
Get pricing and turnaround estimates for regulated multilingual content.
Speak with our team about clinical, regulatory, labeling, or AI-enabled workflows.
Evaluate SesenGPT workflows for multilingual regulated content.
Connect with Sesen for enterprise programs, partnerships, and ongoing support.
Specialized support for global life sciences teams managing regulated multilingual content.
For general inquiries, support, and company information.