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