Category: GMP
Cleaning , Sanitization and Disinfection in pharmaceutical industry Cleaning , Sanitization and Disinfection are most commonly interchanged terms by pharmaceutical professionals but all these terms are different with different …
Material safety data sheets(MSDS) Material safety data sheet is an document which consists of detailed information regarding the product i.e Effects on Health in case of exposure to product. …
Fumigation and Fogging In Pharmaceutical Industry…. The trend in Pharmaceuticals relatively shifted from Fumigation to Fogging as United Nation Environment Protection Agency (UNEPA) , and Occupational Health and Safety …
Contamination and Cross Contamination/Mix ups Contamination and Cross Contamination are two different things needs to be controlled in pharmaceuticals . Contamination is Spoilage of product with unknown Contaminant Cross contamination/Mix …
Static electricity Static electricity is most lightly taken and very harmful thing in pharmaceutical industry . Many incidents have been reported around the world in pharmaceuticals due to static …
Relative Humidity and Dew point… Relative Humidity is readily checked parameters in pharmaceuticals and most misconceived topic . In pharmaceuticals the Drug is prone to degrade in presence of moisture …
Data Integrity and FDA Terminologies.. It is well said that data without integrity is just numbers and letters .FDA(Food and drug administration) expects from pharmaceuticals that the data they …
The View of FDA on Data Integrity. The only tool available for FDA(Food and drug administration) to ensure Identity , Strength and purity of drugs is the data of Drugs …
Form 483 and Warning letters The Perspective of FDA(Food and drug administration) In issuing the Form 483 and Warning letters is to guide the organisation that violation of 21 CFR(code …
GMP and cGMP Myths and truth . GMP and cGMP very common terms for almost all pharmaceutical professionals . GMP refers to good manufacturing practices and cGMP refers to …