Meet Sesen at DIA 2025 in Washington, D.C.
Join us June 15–19 at Booth #2013 to explore global clinical and regulatory language solutions.
- services
Translation & LocalizationRegulatory Translation ServicesMedical & Scientific TranslationClinical Trial TranslationLinguistic Validation ServicesMedical Patent TranslationWebsite Translation & Localization
Labeling Translation ServicesDrug Labeling & Packaging TranslationMedical Device Labeling TranslationIFU (Instructions for Use) TranslationRegulatory Labeling QA
Hybrid Translation & MTPEHybrid Translation (Human + AI)Full MTPE (F-MTPE)Light MTPE (L-MTPE)Regulatory & Scientific MTPE
Software, HealthTech & App LocalizationMedical Device Software LocalizationeHealth & mHealth LocalizationClinical & Medical SoftwareAI Healthcare Application LocalizationPatient Portal Localization
Life Sciences Marketing TranslationMarketing & Commercial TranslationDigital Campaign LocalizationTranscreation & Brand Voice AdaptationMultilingual SEO & Paid Search
Multimedia LocalizationeLearning & Training LocalizationVideo Translation ServicesSubtitling TranslationMultilingual Voiceover ServicesAudiovisual Compliance Translations
Interpreting ServicesOn-site Medical & Clinical InterpretingRemote & Over-the-Phone Interpreting (OPI, VRI)Simultaneous & Consecutive Conference Interpreting
Desktop Publishing (DTP) & FormattingMultilingual Typesetting & LayoutRegulatory Submission FormattingMedical Packaging Design Localization
- sectors
PharmaceuticalsClinical Trial TranslationRegulatory Submission TranslationsDrug Labeling & Packaging TranslationPharmacovigilance & Drug Safety ReportingCMC Documentation Translation
BiotechnologyScientific Research & Publication TranslationPatent & IP TranslationGenomics & Gene Therapy TranslationBiopharmaceuticals & BiosimilarsPreclinical Research Translation
Medical DevicesIFU TranslationRegulatory Compliance TranslationsTechnical Documentation TranslationSoftware & UI LocalizationCER Translation Services
CROClinical Study Documentation TranslationPatient Recruitment & RetentioneCOA Translation ServicesGCP Compliance TranslationsClinical Trial Training Translation
Healthcare & HospitalsPatient-Facing Materials TranslationElectronic Health Records (EHR)Telemedicine & Digital Health TranslationInformed Consent Form TranslationCompliance & Training Translation
Regulatory & GovernmentHealth Authority SubmissionPublic Health & Policy Document TranslationsMedical & Pharmaceutical Legislation TranslationEnvironmental Health & Safety (EHS)International Health Program Documentation
Life Sciences MarketingMultilingual Marketing & BrandingPharmaceutical & Biotech BrochureMedical Device Marketing TranslationDigital Content & Website LocalizationGlobal Conferences & Event Translation
Certifications & Compliance
ISO 17100 | ISO 9001:2015 | ISO 13485:2016 HIPAA-Compliant Workflows FDA, EMA, PMDA Regulatory Expertise
- solutions
Regulatory & Clinical SolutionsRegulatory & Compliance SolutionsMultilingual support for global submissions, labeling, audits, and SOPs.Clinical Trial EnablementTranslations for ICFs, protocols, site documents, and patient recruitment.Pharmacovigilance TranslationSpecialized translations for AE/SAE reports, DSURs, and safety updates.Label Review & In-Context QAIn-layout linguistic QA for packaging, IFUs, and labeling compliance.Modular Submission & Content ReuseComponent-based translation for IDMP, SPL, and XML content workflows.- Commercial & Engagement SolutionsGlobal Product Launch & Market EntryComprehensive support for launching products in international markets.Patient Engagement & RecruitmentCulturally adapted outreach and multilingual trial communications.Terminology Management & HarmonizationConsistent scientific and brand language across markets.E-Learning & Training LocalizationLocalized training for internal teams, HCPs, and external stakeholders.Website & Digital Experience LocalizationTranslation of websites, portals, and mobile health apps.
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