Ras Al khaimah Economic Zone, uae

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A Brief History Of Creation

She was bouncing away, when a cry from the two women, who had
turned towards the bed, caused her to look round.

Clinical Affairs

Experience a practical approach based on your existing regulatory data. Our team supports medical writing of clinical evaluations (MEDDEV 2.7.1.), as well as full-service CRO activities.


In-house knowledge of regulatory and quality requirements facilitates the product-to-market process and provides insight into clinical safety and performance.

Regulatory Affairs

Regulations vary depending on the medical device and market you wish to enter. Our teams offer support for all regulatory compliance issues worldwide.

Quality Assurance

Implement and maintain a Quality Management System (QMS) to ensure your medical device meets certain specifications and requirements.


Choose the expertise that fits your needs
Working with a global team of experts, Qserve manages a diverse array of projects in the medical device industry. Together, we bring your medical device to the global market, complying with international regulations and assuring product quality and safety.

Global Registration

Health authorities determine market approval based on different dossier formats and requirements. With our global network Qserve covers a large percentage of these markets around the world.
We are here to help you for
growth of your business.
Jeddah- Saudi Arabia
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