Regulatory Affairs Consultancy

Ensure Compliance for Medical Devices

Explore Services
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What We DoServices

Our Core Services

Medical Device Registration

Manage EFDA registration process on behalf of manufacturers.

Regulatory Compliance

Expert guidance on Ethiopian regulations.

Pre-Registration Dossier Review

Ensure all documents meet EFDA standards.

Post-Market Surveillance

Monitor device safety & regulatory reporting.

Post-Approval Modifications

Report post-market changes to EFDA on behalf of manufacturers.

Local Representation

Acting as your EFDA liaison in Ethiopia.

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Who We AreAbout Us

What is ?

ETMed is a trusted consultancy specializing in medical device regulatory affairs. With deep expertise in Ethiopian regulations, we help manufacturers navigate complex compliance requirements, ensuring seamless market entry and sustained success.

  • Expertise in EFDA Medical Device Registration
  • Trusted Partner for Global Manufacturers
  • Proven Track Record of Compliance
Why You Should Choose UsOur Updates

What Makes Us Special

Proven Expertise Delivered on Time
Efficiency Backed by Expertise
Your Trusted Industry Partner
Precision, Speed & Expertise in Action
Uncompromising Quality Standards



15+
Total Registration
25+
Global Partners
5+
Years of Experience
6+
No. of Expertise

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