UAE Market Access Guide For Global Medical Device Companies
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A comprehensive handbook covering UAE & Arab medical device market entry, regulatory approvals, business setup, and compliance—explained step-by-step.
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End-to-end UAE medical device market access roadmap
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MoHAP medical device registration & lifecycle compliance
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Company registration, licensing & free zone setup in UAE
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Import–export, customs & distribution compliance
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GCC regulatory comparison & real-world case studies
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Designed for global manufacturers, MedTech startups & regulatory teams
About the Book
Entering the UAE medical device market requires a clear understanding of regulatory approvals, corporate structures, import–distribution rules, and post-market compliance obligations. With the UAE emerging as a regional healthcare hub for the Middle East, Africa, and South Asia (MEASA), global manufacturers must align strategy with regulation.
UAE Market Access Guide for Global Medical Device Companies is a practical, end-to-end handbook designed to simplify the entire UAE and Arab-region medical device ecosystem. The guide bridges the gap between regulation and execution by combining legal frameworks, market intelligence, regulatory pathways, and operational best practices into a single, actionable resource.
Structured for both first-time entrants and established global players, the book offers step-by-step explanations, checklists, strategic insights, FAQs, and real-world case scenarios to reduce risk and accelerate time to market.
What This Book Covers
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Arab & UAE healthcare market overview and growth trends
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UAE medical device market landscape & key segments
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Market entry strategies for global medical device companies
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Legal structures & company registration in the UAE
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Emirate-wise licensing authorities & regulatory portals
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Import–export code, customs clearance & warehousing
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Healthcare & medical device free zones in the UAE
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Manufacturing & assembly of medical devices in the UAE
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Medical device registration under MoHAP regulatory framework
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Licensing for import, wholesale, distribution & retail
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Clinical trials, investigational & compassionate use pathways
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Post-market surveillance, vigilance & medical device recalls
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Advertising, promotion, labeling & HCP interactions
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Regulatory inspections, penalties & compliance strategies
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UAE vs GCC medical device regulatory comparison
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Market entry case studies & common compliance mistakes
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Ready-to-use checklists, templates & reference tools
Who Should Read This Book
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Global medical device manufacturers
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MedTech & IVD companies
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Importers, distributors & local authorized representatives
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Regulatory affairs & compliance professionals
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Healthcare startups entering the Middle East
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Investors & business development teams
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Legal & regulatory consultants
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Professionals targeting UAE & GCC market expansion
Why Buy This Book
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Simplifies complex UAE medical device regulations
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Reduces regulatory, commercial & compliance risks
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Provides practical, execution-focused guidance
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Accelerates UAE & GCC market entry timelines
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Acts as a strategic roadmap for sustainable regional growth
Book Details
Title: UAE Market Access Guide for Global Medical Device Companies
Author: Rajul Jain
Designation: Founder, ELT Corporate Pvt. Ltd.
Category: Healthcare Regulatory | UAE | Medical Devices | Market Access | Compliance
Focus Region: UAE | GCC | Arab Markets

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