Clinical Trail Service

Drawing upon 30 years of experience, we’re here to support progress of your clinical trials with expertise and dedication

Organization of clinical trials and monitoring:

  • Product development studies

  • Selection and supply of reference products and/or test products

  • Generation of study protocols and documentation for Bioethics

  • Pharmacovigilance and safety monitoring service

  • Post-authorization safety studies

  • Import/export and supply of Investigational Medicinal Products (IMP) and Medicines for Clinical trials from non-EU countries

Fill out the inquiry form and receive a consultation, pricing, and a complimentary presentation of our services. Explore collaboration oppurtunities:

The orchestration of clinical trials is a multifaceted endeavor, encompassing critical components that collectively ensure the efficacy, safety, and ethical integrity of medical research. From meticulously crafting study protocols and generating documentation for Bioethics to managing the selection and supply of reference and test products, our organization meticulously navigates the intricacies of product development studies. Our commitment extends to pharmacovigilance and safety monitoring services, playing a pivotal role in safeguarding participant well-being throughout the trials. Post-authorization safety studies further underscore our dedication to long-term safety assessments. Additionally, our expertise in the import/export and supply of Investigational Medicinal Products (IMP) and Medicines for Clinical Trials from non-EU countries solidifies our capability to facilitate global research initiatives seamlessly. Each of these elements converges to form a comprehensive approach, reinforcing the importance of our role in advancing research endeavors with precision, ethics, and international compliance.

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