Services offered
Slavia Pharm offers a wide range of pharmaceutical services for both the domestic market and international partners. Our activities cover all stages of the pharmaceutical manufacturing and quality control process, ensuring product quality, safety, and compliance with European regulatory standards.
GMP Production and Services for Clinical Investigational Products
We provide comprehensive manufacturing services for oral solid dosage forms (tablets, capsules, and sachets) in full compliance with Good Manufacturing Practice (GMP).
- Manufacturing of authorized products and medicinal products for clinical trials
- Processing of tablets, capsules and sachets in series adapted to client requirements
- Modern equipment compliant with European standards
- Primary and secondary packaging services
- Pilot batches for clinical trials
- Traceability and full documentation
- EU batch certification and release
- Monitoring of critical process parameters
- Process validation according to EMA guidelines
- Quality assurance throughout the entire manufacturing process
Quality Control Laboratory (Physical-Chemical and Microbiological)
Slavia Pharm operates an integrated GMP-authorized laboratory that performs rigorous testing of raw materials, packaging materials, and finished products.
- Standardized physico-chemical analysis
- Purity and active substance testing
- Microbiological analysis (bioburden testing, sterility, etc.)
- Validation of analytical methods
- Stability and shelf-life studies
- Equipment calibration and maintenance
- Issuing certificates of analysis
- Investigations for quality deviations
- Support in investigations related to reported adverse reactions
- Laboratory results archiving and traceability
Research, Development and Regulatory Services
Through its dedicated R&D department, Slavia Pharm supports innovation and the continuous development of its product portfolio. These services are provided both for internal projects and for external partners.
- Developing new formulations for RX, OTC and dietary supplements
- Optimizing existing formulas
- Pre-formulation studies
- Technology transfer
- Validation of analytical methods and scale-up production
- Preparation of documentation for product registration
- National and European product registration
- Pharmacovigilance services
- Post-authorization support (variants, extensions, reassessments)
- Regulatory advice and portfolio strategy development
Innovation and Quality in the Pharmaceutical Industry
Modern manufacturing technology
Tailored pharmaceutical solutions
Over 1,000 laboratory tests
High quality standards
Pharmaceutical research and development
Validation and clinical testing
B-dul Theodor Pallady, nr. 44C 032266, Sector 3, Bucharest, Romania
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