Good Manufacturing Practices

Good Manufacturing Practices is defined as system which ensures pharmaceutical products are manufactured with consistent quality standards . GMP is not an Serendipity it is series of developments laid down by professionals by experience, scientific studies and experiments . History has been an witness of many drastic events occurred in history which forced the Regulatory agencies to come forward and make Regulations and guidelines For Food and drug products . in the subsequent articles we will discuss all Discoveries and experiments along with scientific justifications Which attracted regulatory authorities towards them.

• Material Safety Data Sheet In Pharmaceuticals(MSDS)
• Fumigation And Fogging
• Contamination And Cross Contamination
• Static Electricity And Risk Associated In Pharmaceuticals
• Relative Humidity And Effects Of Temperature In Pharmaceuticals
• GMP and cGMP Differentiation
• Data Integrity The Regulatory Challenge
• TSE and BSE In Pharmaceuticals
• Form 483 and Warning Letters
• Data Integrity FDA Perspective
• Cleaning, Sanitization and Disinfection 
• Why 70% IPA Is Used As Disinfectant
• Deviation and Incidence Difference
• Validation/Mapping of Temperature and Relative humidity
• Protection of Light sensitive Drugs
• How GMP changed with time
• Airlocks and its types in pharmaceuticals
• Analytical weighing balance Calibration , Types , Principle,Guidelines.