Medtech

Medtech device services at Registitute Solutions to Accelerate Compliance and Growth in the MENA Region

At Registitute, we offer tailored Medtech device services designed to empower medical technology companies across the MENA region. As a trusted regulatory and market access partner, we help medical device and IVD manufacturers meet compliance requirements, secure product registrations, and succeed in competitive markets.

Our team brings deep expertise in regional and international regulations, including SFDA (Saudi Arabia), EDA (Egypt), and MHRA (UK), offering end-to-end solutions for navigating complex approval processes. Whether you’re launching an innovative device or expanding into new territories, Registitute delivers the regulatory clarity and strategic support you need to move forward with confidence.

Our Medtech device services include:

• Medical device and IVD registration: We manage submissions, technical documentation, and regulatory interactions for swift approvals.

   

• Regulatory strategy and local representation: Get expert planning and in-country representation for Saudi Arabia, UAE, Egypt, and beyond.

   

• Quality management and compliance consulting: Align your operations with ISO 13485, MDSAP, and GxP standards to ensure long-term compliance.

   

• Commercialization support: From early-stage market planning to product launch execution, we support your growth in every step across the MENA region.

   

Our mission is to accelerate access to safe, effective Medtech device services innovations by minimizing regulatory risks and optimizing the approval timeline.

Whether you’re a global manufacturer or a regional innovator, Registitute provides the insight, tools, and hands-on support needed to thrive in the Medtech space.

Contact us today to discover how our Medtech device services can help you navigate regulations and bring your products to market faster and more effectively.