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Publishing

ClinChoice’s publishing teams support the submission processes for medical devices throughout entire product lifecycles for multiple regions worldwide.

  • Global Medical Device Document Publishing Solutions

    • Regulatory Publishing Strategy
    • Regulatory documentation submission services to notified bodies and health authorities
    • Paper to electronic file format conversion in compliance with regional and national regulations
    • Submission readiness reviews using custom quality checklists for compliance with electronic document standards
    • Publishing of clinical reports
    • Document-level and submission-level publishing including but not limited to conversion, optimization, OCR, bookmarking, hyperlinking, document properties, quality review, and validation
    • Gateway submission management to different health authorities, including FDA, TGA, EMA, and other countries