Services
GMP-Certified Pharmaceutical Services
We provide fully compliant, flexible, and customer-oriented pharmaceutical services — from research and development to GMP manufacturing, quality control, stability testing, repackaging, and distribution.
Our integrated capabilities ensure high-quality results, regulatory excellence, and efficient support for partners across Europe and worldwide.
Hoče Manufacturing Facility
Farmakem’s manufacturing facility is located in Hoče, Slovenia and is EU GMP-certified by the Slovenian Agency for Medicinal Products and Medical Devices.
Production Capacity and Capabilities
Production is carried out under controlled and monitored conditions, ensuring compliance with all regulatory and quality standards.
We offer manufacturing solutions for various dosage forms, including liquids, solids and semi-solids.
GMP Custom Manufacturing
Manufacturing Operations - Active Substances
- Primary and Secondary Packaging.
- Analytics in corporation with 3rd party EU GMP analytical lab.
- Storage of incoming materials and finished products.
Manufacturing Operations - Human Medicinal Products
- Primary and Secondary Packaging
- Storage of incoming materials and finished products.
IMPORTATION AND DISTRIBUTION OPERATIONS - ACTIVE SUBSTANCES
- EU GDP license for the international wholesale, import, export and distribution of more than 150 APIs, including prohibited drugs from groups II and III, such as medical cannabis, cannabis extracts, tetrahydrocannabinol and other cannabis products.
Provided Services
We are committed to providing high-quality, flexible and customer-oriented pharmaceutical solutions—from development to delivery.

Research, Development and Design of Formulas
We develop custom pharmaceutical formulas tailored to client needs, from concept to pre-production.

Quality Control
Strict quality checks are performed to ensure all materials and products meet GMP standards.

Development of Validation Processes
We create and manage validation protocols for manufacturing, cleaning, and testing processes.

Analytics
Testing is conducted by certified EU GMP labs, including chemical, physical, and microbiological analysis.

Stability Testing
We perform stability studies to assess product shelf life under different conditions.

Custom Repackaging
We offer primary, secondary, and white-label repackaging of APIs under controlled conditions.

Regulatory Support
Expert assistance with compliance, licensing, and documentation in line with EU pharmaceutical laws.

Storage
Materials and products are stored in monitored, secure environments with temperature and humidity control.

Distribution
GDP-compliant transport with real-time temperature monitoring and full traceability.
Get In Touch With Us
How Can We Assist You?
Share the details of your request and our team will respond promptly.
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Mail us:
info@farmakem.si
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Call us:
+386 262 007 91
Office Hours
Mon–Fri: 8:00 a.m. – 4:00 p.m.
-
Mail us:
info@farmakem.si
-
Call us:
+386 262 007 91
Office Hours
Mon–Fri: 8 a.m. – 4 p.m.
-
Mail us:
info@farmakem.si
-
Call us:
+386 262 007 91
Office Hours
Mon–Fri: 8 a.m. – 4 p.m.
