Clinical trials

Clinical Trial Organization and Monitoring

Our team ensures that every study is conducted with scientific precision, transparency, and in full compliance with ethical and legal requirements. We are committed to supporting our partners throughout all phases of clinical research – from study planning to successful completion.

With many years of experience in the development of pharmaceutical and biological products, Eletis Medica works in close cooperation with clinical trial centers, healthcare institutions, bioethics committees, and international organizations. This collaboration allows us to efficiently manage trial logistics, documentation, and communication, ensuring smooth progress and reliable outcomes.

Our services include:

• Planning and implementation of product development studies;
• Selection and supply of reference products and investigational medicinal products (IMPs);
• Preparation of study protocols and documentation for bioethics committee approval;
• Coordination of study organization and administrative procedures;
• Pharmacovigilance and safety monitoring during clinical trials;
• Post-authorization drug safety assessments;
• Import, export, and supply of investigational medicinal substances and products for clinical trials from non-EU countries.

Eletis Medica ensures complete traceability, accuracy, and quality across every stage of the research process. Our goal is to help partners conduct clinical trials efficiently, meet all regulatory standards, and achieve reliable, evidence-based scientific results.