“My belief is firm in a law of compensation. The true rewards are ever in proportion to the labor and sacrifices made.”
― Nikola Tesla
Clinres Farmacija – Your Global Partner in the Pharmaceutical Industry
Clinres Farmacija is a leading expert in the field of clinical research, regulatory services, pharmacovigilance and quality assurance. Our work is based on the highest standards and regulatory requirements on a global level. With more than 20 years of experience and a wide range of services, we help pharmaceutical and biotechnology companies ensure the compliance, safety and quality of their products – from the early stages of development to post-marketing activities.
Why choose Clinres Farmacija?
Clinical research
At Clinres Farmacija , we conduct comprehensive clinical research that supports the development of new drugs and medical devices. Our team of experts takes care of conducting research at all stages, from planning, data collection to analysis of results. We ensure high quality and compliance with international standards (ICH/GCP), which enables our customers to enter the market quickly and safely. We cooperate with leading pharmaceutical companies in Slovenia, the EU and beyond.
Regulatory Services – Pre- and Post-Marketing
Our team offers comprehensive regulatory services to ensure full compliance with regulatory requirements. Our service includes the preparation of documentation, the registration of medicinal products and medical devices, and coordination with the competent regulatory authorities at the local, European and global level. We assist in obtaining pre- and post-marketing permits and ensuring ongoing compliance with legislation and regulatory guidelines.
Pharmacovigilance
Ensuring the safety of medicines is key to the long-term success of any pharmaceutical product. Our pharmacovigilance services include monitoring, collecting and processing data on adverse reactions, reporting to regulatory authorities and risk management. By constantly monitoring legislation and changes in regulatory requirements, we ensure that all our procedures are in line with the latest guidelines, whether on the national or international market.
Quality assurance
At Clinres Farmacija , we are committed to ensuring the high quality of all our services. Our team closely monitors and improves quality assurance systems that comply with the highest industry standards such as ISO standards, GxP and other regulatory requirements. By ensuring full compliance and accuracy in the implementation of projects, we ensure that our processes are error-free and fully under quality control.
- Expertise and experience: Our team of highly qualified experts combines an in-depth understanding of the industry, the latest scientific practices and regulatory requirements to enable reliable project execution at all stages of the pharmaceutical lifecycle.
- International reach: With our presence in Slovenia, the European Union and more broadly at the global level, we offer a unique blend of local knowledge and a global understanding of the needs of the industry.
- Innovation and flexibility: We keep up with technological developments and changes in legislation, so we can quickly and efficiently adapt to the specific needs of our customers.
- High quality and compliance: All our services consistently meet the latest regulatory and industry requirements, both locally and globally.
- Future-oriented: Our solutions are based on innovative approaches that increase efficiencies, reduce costs and accelerate drug development, while remaining fully compliant with regulatory guidelines and focused on patient safety and well-being.
- Reliability and Ethics: Our commitment to quality, professionalism and ethical operation enables our clients to successfully achieve compliance and support sustainable development and long-term business goals.
20
years of experience
200
executed clinical trials
5000
enrolled patients
550
research sites
