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Editorial Team
H
HRA
Founder & Lead Editor
Medical device regulatory and clinical expert with extensive experience in FDA, EU MDR, and global market access strategies.
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Share your expertise with thousands of medical device professionals worldwide.
What We Look For
- Original regulatory insights
- Expert analysis
- Practical guidance
Benefits
- Reach industry audience
- Build your reputation
- Author bio & links
Contribution Guidelines
Content Requirements
Articles should be 800-2000 words, original, well-researched, and provide actionable insights for regulatory professionals.
Topics We Cover
FDA regulations, EU MDR/IVDR, ISO standards, quality management, clinical trials, post-market surveillance.
Submission Process
Email your article pitch or draft to our editorial team. We review submissions within 5 business days.