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