Qserve CRO’s Cutting-Edge Therapeutic Expertise

When collaborating with Qserve CRO, you unlock the advantages of our extensive expertise spanning a multitude of therapeutic domains. This wealth of experience is harnessed in every project we undertake.

At Qserve CRO, we firmly believe in crafting clinical trials that are finely tailored to the unique requirements of your medical device. Our clinical team boasts a wealth of experience gained from engagements with Notified Bodies, CROs, sponsors, and manufacturers. This fusion of diverse backgrounds, coupled with Qserve’s profound grasp of regulatory affairs, culminates in the development of streamlined and compliant clinical trials.

Our proficiency encompasses a comprehensive array of services, spanning from pre-market to post-market studies encompassing class I through class III devices. Qserve comprehends the intricacies of operational and financial hurdles that accompany medical device clinical trials.

Our Therapeutic Specialties with medical devices

Qserve CRO has full-scope expertise and experience with all types and classified products. Is your device not listed here? Connect with our experts to explore how we can assist you.

Aygul Dereli Oz
“With our broad experience across numerous therapeutic specialties, we know what challenges a clinical trial could face and what it takes to succeed.”
Aygül Dereli Öz / Clinical Project Manager

Qserve’s team has extensive awareness of medical writing, data analysis and broad experience as writers of CEPs and CERs, we can support any medical device manufacturer. Contact us and our team will answer all your questions about our services.

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Latest news

Clinical Suite | Clinical Evaluation under the MDR

Date: 1 May 2023 Time: 18:00 – 21:00 CET | 12-3 pm EST Location: VirtualLanguage: EnglishPrice [...]

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