A master class was organized At the Tashkent Pharmaceutical Institute for Industrial Technology of drugs department on the rules and principles of world standards GMP, GLP, GCP, GDP by the inspector of QA Pharm Product Ruslan Sharipov.
On September 23nd 2019 , at the department of industrial technology of drugs, a master class was held by the inspector of the QA Pharm Product pharmaceutical company Sharipov Ruslan on the topic “GMP” (Good Manufacturing Practice), GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GDP (Good distribution Practice). The lesson of the master class was attended by the teachers of the department, Professor V.R. Khaidarov, associate professor A.D. Tadjieva, associate professor Rakhimova O.R., associate professor Z.Kh. Zufarova, acting Associate Professor M.Sh. Foziljonova, acting Associate Professor R.G. Rakhimov, Associate Professor N.A. Azimova, acting Associate Professor S.T. Sharipova, senior teacher Sh.A. Mamasolieva, assistant R. Masharipova, assistant N. Sadikova, assistant Sh. Husenova and assistant D. Safarova. The master class gave an idea of the rules and principles of pharmaceutical production in accordance with the requirements of GMP – the world standard. GLP is the global standard for requirements for pharmaceutical preclinical research, planning, conducting, preparing documents, analyzing their results, presentation rules and drug requirements, GCP – on global clinical trial standards, as well as the necessary conditions for storage, transportation and distribution in accordance with the requirements of the world standard GDP.
Department of Industrial Technology of drugs: профессор. V.R Xaydarov
