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Julie E
@julieedwards124
Medical Device Regulatory and Compliance Specialist
Canada
English, French, Spanish, German, Italian
About me
I’m a Canada-based regulatory compliance professional helping medical device manufacturers, startups, and global businesses prepare for market entry and certification. I specialize in FDA registration support, EU MDR, CE marking, MHRA, UKCA, ISO 13485, EUDAMED, technical documentation, regulatory gap assessments, and compliance documentation. I focus on clear, accurate, audit-ready work tailored to your product and target market. Let’s turn complex regulatory requirements into a practical compliance roadmap.
Skills
Julie E
Offline •
Average response time: 1 hour
See my services
Technical Writing
I will handle ukca, ce marking, mhra registration and medical device compliance
