ScopeOf Cooperation Description

This page is exclusively for supplier cooperation in the life sciences field (not for corporate client service inquiries). It covers the following types of cooperation, and we sincerely invite partners with medical expertise and compliance qualifications to help build our service ecosystem:

  • 1. Medical Translator / Reviewer Cooperation (requiring a Professional Background in clinical medicine, pharmacy, Medical Devices, or related fields);
  • 2. Medical Localization Technology Suppliers (e.g., Medical Devices software Localization tools and technical support for medical corpora);
  • 3. Medical DTP Formatting Service Providers (requiring proficiency in formatting medical documents such as drug package inserts and Clinical Trials reports);
  • 4. Medical Termbase / Corpus Partners (required to cover medical terminology systems recognized by the FDA/EMA/NMPA);
  • 5. Other Specialized Life Sciences Services (e.g., simultaneous interpretation equipment support for medical conferences and medical translation quality control tools).

Supplier Cooperation Consultation Form

Basic Cooperation Information

Cooperation Type *
Partner Entity Type *
Entity Name *
Contact Person *
Contact Phone *
Contact Email *

Medical Qualification Certification

Professional Qualification Certificate *

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*Supported format: PDF (*Please upload scanned copies/PDFs as required by the cooperation type))
Years of Life Science Service *
Core Service Certification

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*FDA/EMA/NMPA Service Certifications (upload supporting documents if applicable))

Medical Service Capabilities

Specialized Medical Fields *
Past Medical Cooperation Cases *
Language Pairs
Technical Tool Proficiency *

Cooperation Requirements

Desired Cooperation Model *
Service Scope / Capacity *
Preferred Cooperation Duration *

Additional Materials

Client Reviews / Awards

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*Upload client recommendations and medical service awards (e.g., “Medical Translation Service Provider of the Year”))
Remarks

Supplier Cooperation Precautions(coreSpecifications)

  • Qualification Authenticity Requirements (Veto Item)

    All medical service qualification documents (e.g., degrees, CATTI medical certificates, and ISO certifications) must be verifiable through official channels. Falsified qualifications will result in permanent blacklisting.

    Freelance translators must confirm no history of medical translation fraud. Corporate suppliers must provide proof of no medical industry violations or administrative penalties within the past year.

  • Medical Service Professionalism Requirements

    Cases must focus on the life sciences sector; non-medical cases (e.g., general business translation, literary translation) are strictly prohibited.

    Translators must accurately distinguish 'medical terminology differences' (e.g., 'Adverse Drug Reaction (ADR)' vs. 'Adverse Event (AE)'). A medical terminology test will be conducted during the initial cooperation phase (a passing rate of ≥90% is required for cooperation).

  • Data Confidentiality and Compliance Requirements

    All suppliers must sign the “Glyph Translation Life Sciences Supplier Confidentiality Agreement” and comply with HIPAA, ISO 27001, and China’s Data Security Law. Disclosure of clinical trial data, drug formulas, or patient information is strictly prohibited.

    Corporate suppliers must provide a “Medical Data Confidentiality Management Policy” demonstrating secure storage and destruction of sensitive data (e.g., gene sequencing reports).

  • Response and Review Timelines

    Within 3 working days of submission, a Glyph Translation medical cooperation specialist will contact you for an initial qualification review.

    The review takes 7 working days, including terminology testing and case verification. Results will be sent via corporate email. Approved applicants will join the “Glyph Translation Medical Supplier Resource Pool.”

    Unsuccessful applicants may improve their qualifications and reapply after 1 month, specifying the improvements made.

  • Post-Cooperation Management Standards

    Medical translators must complete quarterly “Glyph Translation Medical Terminology Update Training” and pass the assessment to continue undertaking projects.

    Corporate suppliers must submit a “Service Quality Report” every six months. Cooperation will be suspended for rectification if the error rate exceeds 1%.

Contact(Cooperation Questions)

We look forward to partnering with suppliers who possess strong medical expertise, compliance awareness, and confidentiality awareness to jointly enhance the quality of translation services in the life sciences sector and facilitate the efficient global communication of pharmaceutical innovations.

Medical Cooperation Specialist: Mr./Ms. Gao

Consultation Hotline: 400-680-7218 (Weekdays, 9:00–18:00)

Dedicated Email: pm606@oracle-trans.com (Please include 'Supplier Cooperation + Cooperation Type' in the subject line)

Global Consultation Hotline:400 680 7218
21st Floor, Building 19, Zhonghai Xin Innovation Industry City, Jihua Street, Longgang District, Shenzhen