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.

Clinical Research

  • Bioavailability & Bioequivalence studies
  • Pharmacokinetic studies & expert reports
  • Food - drug interactions
  • Population pharmacokinetics/pharmacodynamics
  • Drug interactions

Bioanalytical Laboratories
  • 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

Data interpretation
  • Pharmacokinetic data analysis and statistics are performed using recognized and tested software according to up to date EU and FDA standards.
  • Biostatistics

Pharmaceutical analysis

  • Analysis and study of active substances and of their degradation products in pharmaceutical products.
  • Stability studies in pharmaceutical products.

Microbiological control of pharmaceuticals
  • 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 Services
  • 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.