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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
