Welcome to QureCraft!
Your Partner in Clinical Trial Excellence in Middle East and Central Asia
Who we are?
We are more than a CRO; QureCraft is your committed partner in the pursuit of excellence in clinical research. With a profound understanding of the clinical trial market in Georgia, Kazakhstan, Uzbekistan, Turkey and UAE. Our team combines global CRO expertise with a localised focus. We are dedicated to navigating the intricacies of clinical trials, ensuring compliance, and delivering results that matter.
Why choose Central Asia and Middle East to conduct Clinical Trials?
Strategic Significance of the region
In the dynamic landscape of clinical research, Kazakhstan, Uzbekistan, Turkey, UAE etc emerge as pivotal countries with distinct advantages. We at QureCraft are recognizing the strategic significance of these markets for conducting impactful clinical trials.
Diverse Patient Populations
Regions boast diverse and representative patient populations, enriching the validity and generalizability of clinical trial results. QureCraft's commitment to inclusivity ensures that your trials benefit from a broad spectrum of participants, contributing to robust and comprehensive data
Evolving Healthcare Infrastructure
Countries of these regions are witnessing rapid advancements in their healthcare infrastructure, presenting a conducive environment for clinical research. QureCraft leverages this evolving landscape, providing a platform for cutting-edge trials that align with the latest standards and technologies.
Evolving Healthcare Infrastructure
Countries of these regions are witnessing rapid advancements in their healthcare infrastructure, presenting a conducive environment for clinical research. QureCraft leverages this evolving landscape, providing a platform for cutting-edge trials that align with the latest standards and technologies.
Our Services
With QureCraft, your clinical trials benefit from a comprehensive suite of services that span from inception to completion, ensuring a seamless and successful journey in the dynamic landscape of clinical research.
1
Study Design and Protocol Development
We create clinical trial protocols that comply with international standards and regulatory requirements. Our experienced team designs studies to ensure precise scientific and regulatory compliance, ensuring high scientific validity and data reliability. This allows you to have maximum confidence in the success of your project and its compliance with global clinical practice standards.
2
Site Selection and Feasibility
QureCraft conducts a thorough evaluation and selection of study sites for clinical trials. Our structured approach to site selection, including analysis of their resources and capabilities, as well as conducting feasibility studies, helps reduce risks, improve recruitment, and create conditions for the successful execution of both large and local clinical trials.
3
Regulatory Submission
QureCraft provides comprehensive support in navigating the complex regulatory processes of clinical trials. We streamline the regulatory submission process, ensuring compliance with all local and international regulatory requirements. With our deep knowledge of regulatory processes, we accelerate approvals, which allows us to maintain high clinical trial implementation rates and minimize delays during approval stages.
6
Quality Assurance
At QureCraft, we maintain strict standards, not compromising on the integrity, accuracy and appropriateness of a clinical trial. Our rigorous quality control measures are designed to exceed industry standards and provide confidence that the trial is ethical, effective and in line with international best practice. We ensure that every trial is conducted to the highest standard, maintaining our reputation as a trusted partner in clinical research.
5
Data Management and Analysis
Data collection and analysis are key to the successful execution of any clinical trial. QureCraft uses modern data management methods to ensure data accuracy, reliability, and security. Our team of analysts transforms raw data into valuable insights, enabling informed decision-making at every stage of your study. We maintain high levels of data quality to achieve scientific goals and meet regulatory requirements.
4
Project Management
QureCraft provides professional project management covering all aspects of your clinical trial. Our team of experts coordinates processes, monitors the completion of all tasks within the established deadlines and maintains high quality standards at every stage. We closely monitor the progress of the study, promptly eliminate risks and ensure its successful completion in accordance with planned indicators and regulatory requirements.
Therapeutical areas expertise
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Cell and gene therapy
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Diseases of the cardiovascular system
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Diseases of the Central Nervous System
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Endocrinology
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Infectious diseases and vaccines
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Nephrology
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Nephrology
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Oncology
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Ophthalmology
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Pediatrics
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Pulmonology
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Rheumatology
Contact us
Contact QureCraft for Tailored Clinical Trial Solutions
8 THE GREEN, STE B, DOVER, KENT, DELAWARE, USA 19901
+1 310 985 16 43
+1 347 354 1820