Quality findings
Accuracy, terminology, technical precision, and critical error observations.
SesenGPT Life Sciences Benchmark Program
See how SesenGPT compares with your existing translation process through an evidence-based evaluation using representative clinical, regulatory, and technical content.
Assess translation accuracy, terminology, human review effort, turnaround, and total cost using quality requirements that matter to your organization.
Evaluate new capabilities without replacing your existing provider.
Your Benchmark Findings
A useful benchmark goes beyond AI output or translation speed. It measures the quality achieved, time spent, review effort, and cost required to produce an accepted final translation.
Accuracy, terminology, technical precision, and critical error observations.
Corrections and expert-review effort required before acceptance.
End-to-end turnaround and cost measures where comparable data exist.
Where SesenGPT may help and where human-led controls remain essential.
Side-by-side findings based on your agreed evaluation criteria.
No results are shown. Actual findings depend on the agreed scope and available baseline information.
Evaluation Criteria
Regulated life sciences content requires more than fluent first drafts. The benchmark assesses technical accuracy, applicable regulatory content requirements, and the human review needed to reach the agreed final quality threshold.
Review meaning, completeness, technical accuracy, and the severity of errors that matter to the intended use.
Check approved scientific, product, and regulatory terminology and alignment with applicable content requirements.
Assess dosages, values, units, warnings, technical instructions, and content completeness.
Measure necessary edits, reviewer time, and rework needed to reach the agreed quality threshold.
Compare translation, review, corrections, and end-to-end delivery rather than raw processing speed.
Examine translation, linguistic review, corrections, and measurable internal review effort using comparable assumptions.
Fair comparisons, defined in advance. We agree on source content, language pairs, quality thresholds, reviewer roles, and evaluation methods. Where possible, both workflows are assessed with consistent materials and reviewers separate from translation production. Any differences or missing baseline data are disclosed in the findings.
A defined, four-step evaluation designed for informed translation decisions without a company-wide localization change.
Agree on representative documents, language pairs, quality requirements, and the measures that matter to your team.
Identify comparable existing-workflow translations, language assets, review requirements, and available cost or time data.
Evaluate SesenGPT output through controlled workflows and qualified linguistic review using agreed scoring criteria.
Discuss the comparative results, any baseline limitations, and practical options for future translation workflows.
Start with representative content. Keep your current provider and operations in place while you evaluate alternative workflows.
Discuss an EvaluationLife Sciences Specialization
We tailor benchmark language pairs, terminology resources, qualified review, and quality criteria to each document's intended use and risk profile.
Protocols, informed consent, investigator materials, patient communications, and study documentation.
Clinical Trial Translation ServicesSubmission materials, health authority correspondence, CMC documentation, and controlled updates.
Regulatory Translation ServicesIFUs and eIFUs, product labeling, technical documentation, device software, and interfaces.
Medical Device Translation ServicesWe can also evaluate pharmaceutical labeling, drug safety communications, biotechnology and advanced therapy documentation, eCOA/ePRO, digital health interfaces, and scientific content.
SesenGPT combines life sciences-adapted AI with approved language assets, medical linguist review, and structured quality assurance.
No provider switch is required. Confidentiality requirements, secure transfer arrangements, access controls, and necessary agreements are established before samples are exchanged. Representative or de-identified content may be appropriate.
Practical answers about evaluation criteria, confidentiality, comparative data, and participation.
It is a structured evaluation comparing SesenGPT-enabled translation with your existing workflow or agreed baseline using representative content, defined quality criteria, and available operational data.
Yes, when comparable source content, permitted reference translations, and baseline data are available. If a direct comparison is not possible, we can assess SesenGPT against agreed requirements and explain the limitations of the results.
Depending on scope, measures may include technical and linguistic accuracy, terminology adherence, critical errors, numerical precision, reviewer corrections, turnaround, and total cost per accepted deliverable. Criteria and quality thresholds are agreed before evaluation.
A findings summary covering the agreed performance measures, key quality observations, limitations in the available comparison, and recommendations for suitable next steps. The depth and format of the findings are determined with your team during scoping.
Representative clinical trial, regulatory, pharmaceutical, medical device, biotechnology, and digital health content may be evaluated. Sesen supports more than 150 languages; the benchmark language pairs are selected based on scope and available specialist resources.
Before project materials are exchanged, we establish confidentiality needs, approved transfer methods, access controls, and necessary agreements. Representative or appropriately de-identified content may be used where suitable.
No. You can participate without replacing your current translation provider. Qualified medical and linguistic reviewers remain central to assessing final quality; the benchmark identifies where AI assistance may help and where more human oversight is required.
The benchmark compares measurable translation results with an existing workflow or defined baseline. A pilot evaluates broader operational fit, workflows, and adoption possibilities. Both can inform future localization decisions. Explore the SesenGPT pilot.
The scope, schedule, deliverables, and commercial terms depend on document volume, complexity, language pairs, and review requirements. These are established with your team before work begins.
Start Your Evaluation
Bring a representative project, your current quality expectations, and the priorities you want to measure. Our life sciences team will help define a practical comparison.
Loading the benchmark form. If it does not appear, contact our life sciences team.
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.
Digital health platforms, patient portals, eCOA, and clinical software.
Health authority, public health, policy, and compliance-driven communication.
Public health programs, policy documents, and global health initiatives.
Patient-facing content, EHR documentation, telehealth, and care communication.
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.
Life Sciences Translation Company
Sesen helps life sciences teams manage clinical, regulatory, labeling, and AI-enabled translation workflows across 150+ languages.
Trusted by life sciences teams for regulated multilingual content across clinical, regulatory, labeling, and healthcare workflows.
Services
Life Sciences Language Services
Explore Sesen services for clinical, regulatory, labeling, medical device, software, multimedia, and global commercial content.
Featured Services
ICFs, protocols, site documents, and patient-facing materials.
Submissions, SOPs, audits, and regulated documentation.
Labeling, packaging, and product content for global markets.
Instructions for use and medical device documentation.
More Services
COA, PRO, questionnaire, and instrument workflows.
Specialized translation for medical and scientific content.
Software, portals, apps, and connected health interfaces.
Video, voiceover, subtitles, and training content localization.
Remote and onsite interpreting for life sciences settings.
Commercial, launch, and market access content for global audiences.
Need Help Choosing?
Discuss clinical, regulatory, labeling, or AI-enabled translation needs with a life sciences specialist.
Life Sciences
Life Sciences
Explore Sesen support for pharmaceutical, biotechnology, medical device, CRO, healthcare, public health, and regulated content teams.
Core Life Sciences Sectors
Healthcare & Public Sector
Specialized Domain Expertise
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.
Trust & Compliance
Plan a Global Program
Connect with Team Sesen to review clinical, regulatory, labeling, or AI-enabled multilingual workflow needs.
Explore structured multilingual workflows for clinical, regulatory, labeling, commercial, training, and patient engagement programs.
Global submissions, labeling audits, SOPs, and regulated documentation.
ICFs, protocols, site documents, patient materials, and recruitment content.
Structured workflows for labeling translation, validation, and approval.
In-layout linguistic QA for packaging, IFUs, labeling, and compliance.
AE and SAE reports, DSURs, safety updates, and surveillance content.
Component-based translation for IDMP, SPL, and XML content workflows.
Support for launching products across international markets.
Culturally adapted outreach and multilingual trial communications.
Consistent scientific and brand language across global markets.
Localized training for internal teams, HCPs, and external stakeholders.
Websites, portals, mobile health apps, and digital patient experiences.
Sesen combines expert linguists, validation-driven review, and AI-assisted technologies to support global life sciences operations.
EXPLORE SESENGPTConnect with Team Sesen to discuss clinical, regulatory, labeling, commercial, or AI-enabled multilingual operations.
AI & Innovation
AI
Powered by SesenGPT workflowsExplore Sesen AI workflows for translation, terminology, validation, labeling, clinical trials, regulatory content, safety, and digital health localization.
Core AI Platform
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.
Operational AI Solutions
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.
Controlled AI Translation Program
Start with a pilot that combines SesenGPT, professional native medical linguists, terminology control, and validation-driven QA.
EXPLORE SESENGPTDiscuss AI Workflows
Connect with Team Sesen to discuss AI-assisted translation, terminology governance, multilingual QA, and regulated life sciences workflows.
Resources
Resources
Explore all resourcesAccess expert perspectives, proof points, learning resources, and practical tools for multilingual life sciences content programs.
Industry Insights
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.
Customer & Operational Resources
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.
Strategic & Technical Resources
AI Translation Guidance
Review insights on validation, terminology, structured content, compliance, and multilingual operations for life sciences organizations.
Explore AI InsightsResource Center
Explore Sesen resources for clinical, regulatory, AI-enabled, quality, and multilingual content operations.
Learn about Sesen's mission, leadership, values, global footprint, partners, and commitment to life sciences localization excellence.
Company Foundation
Global Presence
Why Teams Work With Sesen
Sesen combines life sciences specialization, multilingual operations, and AI-enabled workflows for organizations that need quality, consistency, and scale.
Talk With Team Sesen
Connect with Team Sesen to discuss enterprise translation, localization, or AI-enabled workflow needs.
Contact
Contact
Talk with our teamChoose the right path for a new translation, localization, AI-enabled workflow, partnership, or existing project support need.
Start a Project
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.
Enterprise Engagement
Why Organizations Contact Sesen
General Contact Information
For general inquiries, support, and company information, connect with Team Sesen and we will route your request to the right team.