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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.
Training
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.
SERVICES
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.
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.
