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Access
to international markets

​QureCraft is your partner
in clinical research

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We combine the global expertise of a contract research organization with deep knowledge of local markets, ensuring high-quality data, compliance with international and local standards, and fast project execution. Our team, with over 20 years of experience in international research and drug launches in the US, EU, and other countries, successfully helps companies navigate all stages of clinical trials and register drugs in any market

QureCraft — your reliable partner in clinical research and market access in North America, CIS countries, Central Asia, and the Middle East

More than a CRO

Development of market entry strategy for medical products

A clear, step-by-step plan focused on results

Our team develops customized market entry strategies for medical products, based on a thorough analysis of market conditions, regulatory requirements, and the needs of target segments. We minimize risks, optimize resources, and accelerate the launch process, ensuring your product gains a competitive edge in the market

Study design and protocol development

A scientifically grounded approach to every stage of the research

We develop clinical trial protocols based on international standards and regulatory requirements, ensuring a high degree of data validity and reproducibility. Our solutions reduce preparation time and minimize the risk of rejections, facilitating the successful and timely progression of your project

Submission of documents to regulatory authorities 

Reducing approval times through an optimized submission process.

We offer expert support at every stage of interaction with regulatory authorities. Our specialists ensure full compliance of documentation with regulatory requirements, significantly speeding up the approval process and minimizing the likelihood of rejections.

Project management and monitoring

Professional oversight of all stages of the study for maximum efficiency.

Our specialists manage projects at all stages, from planning to completion, ensuring adherence to timelines, quality, and regulatory standards. We promptly identify and mitigate risks, ensuring the successful completion of the study within the established parameters

Consulting and regulatory support

Expert guidance for successful interaction with regulatory authorities

We offer comprehensive consulting services, including assistance with the preparation and submission of documents to regulatory authorities. Our experts provide accurate guidance on regulatory compliance, helping to accelerate the approval process and avoid unnecessary delays

Investigating drug application in Real-World clinical practice

Evaluation of the efficacy and safety of drugs in real-world conditions

We conduct studies focused on the use of pharmaceuticals in everyday medical practice to accurately assess their long-term efficacy and safety. These studies provide insights into real treatment outcomes, improve clinical practice, and generate valuable data that can influence regulatory decisions and clinical recommendations for healthcare professionals.

Therapeutic expertise

  • Cell and Gene Therapy
    Our knowledge and experience allow us to conduct clinical trials flawlessly for these advanced treatments, including CAR T-cell therapy studies. With a well-established network of partner centers and a deep understanding of regulatory requirements, we assist partners in implementing innovative therapies aimed at addressing pressing medical challenges
  • Cardiovascular Diseases
    We have extensive experience in managing complex cardiovascular disease trials. Our global network of centers and therapeutic expertise enable us to successfully execute projects of any scale
  • Central Nervous System (CNS) Diseases
    From Alzheimer's disease to epilepsy, we conduct clinical trials for CNS treatments, effectively overcoming challenges related to patient recruitment, retention, and complex protocols
  • Endocrinology
    Whether it's diabetes or other hormonal disorders, we have extensive experience conducting research in the field of endocrinology. By utilizing real-world data and patient-centric solutions, we accelerate the path to regulatory approval and drug registration.
  • Infectious Diseases and Vaccines
    Our vast experience in infectious diseases and vaccine development is backed by a history of successful global studies. Through innovative center management and meticulous monitoring, we ensure high-quality implementation of trials
  • Nephrology
    We offer a comprehensive approach to clinical research in kidney and urinary tract diseases. Our team combines deep scientific knowledge with innovative methods, optimizing study design, minimizing risks, and accelerating the development of effective solutions for patients.
  • Cell and Gene Therapy
    Our knowledge and experience allow us to conduct clinical trials flawlessly for these advanced treatments, including CAR T-cell therapy studies. With a well-established network of partner centers and a deep understanding of regulatory requirements, we assist partners in implementing innovative therapies aimed at addressing pressing medical challenges
  • Cardiovascular Diseases
    We have extensive experience in managing complex cardiovascular disease trials. Our global network of centers and therapeutic expertise enable us to successfully execute projects of any scale
  • Central Nervous System (CNS) Diseases
    From Alzheimer's disease to epilepsy, we conduct clinical trials for CNS treatments, effectively overcoming challenges related to patient recruitment, retention, and complex protocols
  • Endocrinology
    Whether it's diabetes or other hormonal disorders, we have extensive experience conducting research in the field of endocrinology. By utilizing real-world data and patient-centric solutions, we accelerate the path to regulatory approval and drug registration.
  • Infectious Diseases and Vaccines
    Our vast experience in infectious diseases and vaccine development is backed by a history of successful global studies. Through innovative center management and meticulous monitoring, we ensure high-quality implementation of trials
  • Nephrology
    We offer a comprehensive approach to clinical research in kidney and urinary tract diseases. Our team combines deep scientific knowledge with innovative methods, optimizing study design, minimizing risks, and accelerating the development of effective solutions for patients.
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Adjuvant TNBC*

Situation

A U.S.-based biopharmaceutical company faced challenges recruiting patients with triple-negative breast cancer for a Phase II clinical trial.

Result

Patient enrolment was successfully completed 2.5 months ahead of schedule. Two of the seven selected sites became top recruiters among all 25 sites participating in the trial and successfully passed audits.

Solution

We proposed adding additional countries to the trial. In these countries, we initiated work at seven sites and conducted a patient outreach campaign. This campaign was targeting  both treating physicians and patients.

We will develop the best solution for your purposes

USA
8 THE GREEN, STE B, DOVER, KENT, DELAWARE, USA 19901 
+1 310 985 16 43
+1 347 354 1820
info@qurecraft.com

​«QureCraft Eurasia» 
Kazakhstan, Almaty city,
54/19 KENESARY KHAN Street info@qurecraft.com

© 2024 QureCraft Innovations Inc.

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