If you operate in the healthcare, pharmaceutical, or medical device industry, obtaining approval from the UAE Ministry of Health and Prevention (MOHAP) is essential before any product can enter the market. From medical device classification to full MOHAP registration in the UAE, every healthcare product must meet strict regulatory requirements.
Registered pathways
Nextmove provides expert support for MOHAP product registration, medical device classification, and regulatory licensing, ensuring your healthcare products comply with UAE healthcare regulations. Our team guides manufacturers, importers, and distributors through the entire approval process — helping you secure MOHAP regulatory approval efficiently and without unnecessary delays. With our dedicated MOHAP registration services in the UAE, businesses can avoid costly mistakes, documentation errors, and long approval times. We manage the full process from product evaluation and medical device classification to final submission through the official MOHAP regulatory system, helping your products enter the UAE healthcare market faster.
From single-device imports to full multinational healthcare portfolios, we handle every product category regulated under MOHAP and the Emirates Drug Establishment (EDE).
Our MOHAP import clearance service helps healthcare companies obtain the required permits for importing medical devices and pharmaceutical products into the UAE. We assist with regulatory documentation, customs approvals, and compliance with Ministry of Health and Prevention requirements.
Medical device classification is a critical step in the MOHAP registration process. Devices are categorized based on risk levels to determine the regulatory pathway required for approval. Our experts help companies identify the correct classification to ensure smooth product registration.
Medical device registration with MOHAP ensures healthcare products meet UAE safety and regulatory standards. We assist manufacturers and distributors with documentation preparation, regulatory submissions, and compliance to obtain market approval.
Foreign manufacturers must appoint an authorized representative in the UAE for MOHAP medical device registration. Our service ensures regulatory communication, documentation management, and compliance with UAE healthcare authority requirements.
Every engagement follows the same structured pathway. You always know what stage you're at, what's next, and who's handling it.
Free 30-minute call to map your category, timeline and cost.
We review formulations, artwork, and manufacturer documents.
Full CPRE submission via the Montaji portal with our specialist.
We manage authority feedback and clarifications on your behalf.
Digital approval certificate delivered — ready for customs.
Requirements vary slightly by sub-category, but the core dossier is consistent. We audit every document before submission so nothing bounces back.
Indicative ranges based on typical cases. Exact scope and fees are confirmed after your free consultation.
| Category | Typical timeline | Common approvals |
|---|---|---|
| Medical Device (Low risk – Class I/A) | 15–20 working days | EDE (formerly MOHAP) |
| Medical Device (Medium risk – Class II/III, B/C) | 20–35 working days | EDE |
| Medical Device (High risk – Class IV/D, IVD) | 30–45+ working days | EDE |
| Healthcare/Pharma Product (verified pathway – prior FDA/EMA/MHRA approval) | 3–6 months | EDE |
| Import Permit (per shipment, post-registration) | 3–10 working days | EDE, Customs |
Still have questions? Our regulatory specialists respond within 24 hours.
Book a 30-minute call with our regulatory specialists. We'll map the fastest pathway for your category and share a clear cost and timeline estimate.
Fill out the form and our team will be in touch within 24 hours.
