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Tagname : medical device certification

  • TUV Rheinland Opens Fast-Track ISO 13485 Remote Review for China
    TUV Rheinland launches a fast-track ISO 13485 remote review for China, helping Remote Monitoring device makers speed EU MDR compliance, cut delays, and improve certification readiness.
  • China's Pharma License-out Hits $59.6B in Q1 2026
    China's Pharma License-out hits $59.6B in Q1 2026 — discover how system-integrated hardware-software innovations are reshaping global biopharma partnerships and creating new growth levers.
  • ZLG Extends API Security Audit Deadline for Sterilization Systems to Jun 15, 2026
    API security audit deadline for sterilization systems extended to Jun 15, 2026 — critical for Chinese medtech exporters to EU. Act now to avoid CE marking suspension.
  • ZLG Updates Sterilization Cloud Access List: 21-Day API Audit Window for Chinese Vendors
    ZLG updates Sterilization Cloud access: Chinese vendors must complete ISO/IEC 27001 API audit by June 10, 2026—protect CE marking & EU market access now.

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