Drug Quality Control in Kenya: Observation in the Drug Analysis and Research Unit During the Period 2001-2005

  • G N THOITHI
  • K. O. ABUGA
  • J. M. NGUYO
  • O. K. KING’ONDU
  • G. G. MUKINDIA
  • H. N. MUGO
  • J. K. NGUGI
  • I. O. KIBWAGE
Keywords: Quality control, active pharmaceutical ingredient content, dissolution

Abstract

During the five-year period January 2001 to December 2005, the Drug Analysis and Research Unit received and analyzed 394 drug samples. Samples were received from regulatory authorities, local industry, non-governmental organizations, hospitals and private practitioners. The samples analyzed constituted 37.8 % locally manufactured and 62.2 % imported products. In contrast to previous years when failure rates of over 20 % were recorded, the overall rate of failure to comply with compendial quality specifications was 6.1 %, comprising of 8.7 % locally manufactured and 4.5 % imported drugs.

Published
2018-11-14
How to Cite
THOITHI, G., ABUGA, K., NGUYO, J., KING’ONDU, O., MUKINDIA, G., MUGO, H., NGUGI, J., & KIBWAGE, I. (2018). Drug Quality Control in Kenya: Observation in the Drug Analysis and Research Unit During the Period 2001-2005. The East and Central African Journal of Pharmaceutical Sciences, 11(3), 74-81. Retrieved from https://uonjournals.uonbi.ac.ke/ojs/index.php/ecajps/article/view/81