Search results
Results from the WOW.Com Content Network
Three types of courses are conducted by PCB; Category A for undergraduate level, Category B for diploma certificate courses of one to three years duration, and Category C for three-month courses. [6] Bangladesh Pharmacy Council grants certificates after completion of various training and education in pharmacy from various educational ...
A pharmaceutical Company . The pharmaceutical industry in Bangladesh is one of the most developed technology sectors within the country. Manufacturers produce insulin, hormones, and cancer drugs. This sector provides 97% of the total medicinal requirement of the local market.
13. Diploma in Garments Design & Pattern Making Engineering; 4-year program affiliated with Bangladesh Technical Education Board 14. Diploma in Laboratory Medical Technology; 4-year program affiliated with Bangladesh Technical Education Board 15. Diploma in Pharma Technology; 4-year program affiliated with Bangladesh Technical Education Board
🧪Pharmaceutical Analysis Laboratory; 🧪Physiology and Pharmacology Laboratory; 🧪Pharmaceutical Microbiology Laboratory; 🧪Pharmaceutical Technology and Cosmetology Laboratory; 🧪Biopharmaceutics and Pharmacokinetics Laboratory; Research Laboratory: 🧪Centre for Advanced Biomedical Research Laboratory
The Bangladesh Technical Education Board is a state regulatory board responsible for monitoring and developing technical and vocational education in the secondary level (SSC), 2-year higher secondary level (HSC/Vocational), 4-year Diploma in Agriculture, 4-year Diploma in Engineering degree and 4-year Diploma in Medical Technology degree throughout the People's Republic of Bangladesh. [1]
The Board of Trustees of Santosh Islami University submitted a proposal to the government to establish a science and technology university in Santosh. The prime minister of Bangladesh Sheikh Hasina laid the foundation-stone of MBSTU at Santosh, Tangail in 1999. Aminul Hoque was appointed as the founder project director on 7 January 2001.
Process analytical technology (PAT) has been defined by the United States Food and Drug Administration (FDA) as a mechanism to design, analyze, and control pharmaceutical manufacturing processes through the measurement of critical process parameters (CPP) which affect the critical quality attributes (CQA).
More specifically, the ISPE's guide The Good Automated Manufacturing Practice (GAMP) Guide for Validation of Automated Systems in Pharmaceutical Manufacture describes a set of principles and procedures that help ensure that pharmaceutical products have the required quality. One of the core principles of GAMP is that quality cannot be tested ...