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A Turkish Organization that Offers Clinical Research and Registration of Pharmaceutical Products and Medical Devices is Seeking Commercial Agreements.

Summary

Profile Type
  • Business Offer
POD Reference
BOTR20240925010
Term of Validity
9 December 2024 - 9 December 2025
Company's Country
  • Turkey
Type of partnership
  • Commercial agreement
Targeted Countries
  • All countries
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General information

Short Summary
An organization based in Türkiye, established in 2008, specializes in clinical research and the registration of pharmaceutical products and medical devices. Operating under ethical standards and in compliance with Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) regulations, the organization adheres to Turkish Medicines and Medical Devices Agency (TİTCK) and European Medicines Agency(EMA) guidelines. It seeks commercial partners for agreements to expand its services.
Full Description
Founded in 2008 in Kayseri, this organization specializes in clinical research, focusing on developing and registering pharmaceutical products and medical devices. The organization conducts all studies in strict adherence to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and ethical standards, ensuring compliance with the Turkish Medicines and Medical Devices Agency (TİTCK) and the European Medicines Agency (EMA) regulations.

Services include:
- Bioavailability / Bioequivalence Studies
- Phase I-II-III and Observational Clinical Trials
- Clinical Trial Services
- Project Management & Clinical Trial Management
- Ethical and Ministry Applications
- Medical Writing & Consultancy Services
- Statistical Analysis & Data Management
- Clinical Trial Support Services

The organization seeks commercial partners to enhance pharmaceutical and medical device capabilities. Collaborating will allow partners to leverage expertise in clinical research for product development and regulatory submission processes.
Advantages and Innovations
- Adherence to Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) standards.
- Offers bioavailability studies, project management, and statistical analysis.
- Utilizes advanced techniques for efficient study design and data management.
- Committed to delivering high-quality outcomes in all research activities.
Stage of Development
  • Already on the market
Sustainable Development Goals
  • Goal 12: Responsible Consumption and Production
  • Goal 4: Quality Education
  • Goal 17: Partnerships to achieve the Goal
  • Goal 3: Good Health and Well-being
IPR status
  • No IPR applied

Partner Sought

Expected Role of a Partner
- Provide Regulatory Support
- Share Resources and Expertise
- Assist in Data Management
- Promote Research Findings
Type and Size of Partner
  • SME 11-49
  • SME <=10
  • SME 50 - 249
  • Other
  • Big company
  • R&D Institution
  • University
Type of partnership
  • Commercial agreement

Dissemination

Technology keywords
  • 06001002 - Clinical Research, Trials
  • 09006002 - Technical Standards
  • 06001015 - Pharmaceutical Products / Drugs
  • 03004007 - Pharmaceutics
  • 09006001 - Quality Standards
Market keywords
  • 05007002 - Pharmaceuticals/fine chemicals
  • 05005022 - Other clinical medicine
Sector Groups Involved
  • Health
Targeted countries
  • All countries