We provide an integrated package of services to the pharmaceutical industry including clinical research, drug analysis, report writing and regulatory expertise.
All studies are conducted in full compliance with the GLP & GCP regulations.
- Bioavailability & Bioequivalence studies
- Pharmacokinetic studies & expert reports
- Food - drug interactions
- Population pharmacokinetics/pharmacodynamics
- Drug interactions
- Analytical method development
- Biological samples. Drugs and their metabolites, drugs of abuse, protein chromatographic analysis, etc.
- Comprehensive instrumentation HPLC,GC, or mass spectrometry (GC/MS) detection, immunoassay services
- Pharmacokinetic data analysis and statistics are performed using recognized and tested software according to up
to date EU and FDA standards.
Microbiological control of pharmaceuticals
- Analysis and study of active substances and of their degradation products in pharmaceutical products.
- Stability studies in pharmaceutical products.
- Routine microbiological analysis (Total number of microorganisms, control for the absence of pathogensÉ)
- Challenge tests - Control of the efficacy of antibacterial ingredients
- Consulting services, etc.
- Regulatory consultation
- Creation and / or filling of regulatory documents
- Services are provided for the approval of new pharmaceutical products in compliance with Authorities demands.
Consulting, Research activities & training workshops in pharmaceuticals.
- Research studies on specific projects in pharmaceuticals Aspects of analytical organic chemistry, including preparative chromatography. Also, isolation, purification, characterization of bioactive components from natural products.
- Consulting services in the development of new products.
- Training courses and Workshops are organized for the personnel of the Pharmaceutical Industry.