Medical Translation
Where Linguistic Precision Meets Medical Compliance.
Since its inception, SuccessGlo has specialized in delivering mission-critical language solutions tailored to the exacting requirements of pharmaceutical innovators, medical device manufacturers, and biotechnology enterprises. We recognize that medical translation transcends linguistic conversion—it is a foundational element of patient safety, regulatory adherence, and commercial viability. Our approach integrates domain-specific expertise with ISO-certified quality management systems to ensure technical accuracy and compliance across all deliverables.
We enable manufacturers to navigate multilayered regulatory pathways, mitigate submission risks, and expedite market authorization globally. From initial concept to post-market lifecycle management, partner with SuccessGlo to transform precision translation into a strategic asset—ensuring safe, compliant, and timely access to life-sustaining drugs and medical technologies worldwide.
Leveraging a multidisciplinary team of linguists, regulatory specialists, and subject-matter experts, we deliver 3,000+ certified medical translation projects annually, spanning 60+ languages and 30+ therapeutic domains. Our proprietary terminology management systems and AI-enhanced validation workflows ensure consistency across all kinds of drugs, complex device classifications (Class I-III) and emerging IVD/software-as-a-medical-device (SaMD) sectors. All of our projects undergo:
- dual-phase linguistic validation
- medical terminology alignment
- regulatory compliance checks against target market(s)
As one of the few language service providers triple-certified to ISO 9001 (Quality Management), ISO 17100 (Translation Services), and ISO 27001 (Information Security), we support the full spectrum of pharmaceutical and medical device developments and post-market requirements. Our services encompass:
- Pharmaceutical dossiers: chemical drugs, biologics (mAb, vaccines, gene therapies, etc.)
- Medical technologies: full-spectrum device documentation
- Health products: cosmetic ingredient files, dietary supplement claims, biocidal product registrations
- Informed Consent Forms (ICF) and protocols
- Investigator’s Brochures (IB) and patient narratives
- Statistical Analysis Plans (SAP) and tables/listings/figures
- China CDE and CMDE
- EU EMA
- Japan PMDA
- USA FDA
- Vietnam DAV and IMDA
- Periodic Safety Update Reports (PSUR)
- Suspected Unexpected Serious Adverse Reaction (SUSAR) filings
- Company Core Data Sheets (CCDS)
Technical and Compliance Documentation
- Labels of drugs and medical devices
- IFU (Instructions for Use)
- Embedded software and analysis platforms for medical devices
- User and service manuals
- CME-accredited training modules
- Peer-reviewed journal manuscript preparation
- Patent filings
Certified On-Site/Remote Interpretation
- Pre-IND/IDE consultations
- Health authority interactions (CDE, FDA, PMDA panels)
- Drug and medical device exhibitions (CMAC, RSNA, ESC)
- Investigator meetings and DSMB sessions
Have a Project That Needs Translation?
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