Chapter 3

GMP in Pharma Manufacturing—Description of GMP as Related to Air-Handling Units and Prevention of Contamination and Implementation of GMP Regulatory Requirements

S. Lakshmana Prabu1, T.N.K. Suriyaprakash2, K. Ruckmani1 and R. Thirumurugan3,    1Anna University, Tiruchirappalli, Tamil Nadu, India,    2Al Shifa College of Pharmacy, Kerala, India,    3International Medical University, Kuala Lumpur, Malaysia

Abstract

Drug substances and drug products are used for treating various diseases to save the lives of human beings. Drug substances and drug products should be manufactured using clean equipment with appropriate quality and in good environmental condition to avoid contamination of the product and to produce the desired therapeutic ...

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