An experienced QA and QC analyst over 8 years in national pharmaceutical regulatory authority. Have got the complete picture of how a WHO accredited laboratories work in analyzing pharmaceutical products. Well acquainted with all the physical and chemical analytical procedures used for the analysis of pharmaceutical products. My experience extended during these years and hence after, in the assessment of the pharmaceutical dossier (Volume II), GMP audits to local and foreign drug product pharmaceutical manufacturers prior to their registration/approval, Safety officer, Quality assurance and regulatory affairs as variation assessor.