Purpose Pharmaceutical manufacturers execute quality control operations and Good Manufacturing Practices (GMP) to provide safe drugs. The Federal Drug and Food Administration (FDA) is tasked with ensuring manufacturers are performing such procedures. Faced with limited resources the FDA has developed novel tools to aid pharmaceutical manufacturing oversight. This paper briefly reviews these tools. Methods Current inspection approaches employed by the FDA are identified by searching the FDA’s guidances, the Code of Federal Regulations, public reports and other online resources. Outcomes Industry A risk-based site selection model (SSM) is used to prioritize on-site inspections for FDA investigators. Theoretically, the SSM allows FDA investiga...
There has been an increasing trend in the number of prescribed and over-the-counter drug recall over...
This paper describes USP-NF compendial updates to six ‘high-priority ” excipient monographs: Glyceri...
Background: United States Food and Drug Administration (FDA) is the fastest drug review agency in th...
This research details the FDA\u27s quality systems methodology used in its inspection of biopharmace...
This research describes how the FDA has incorporated risk analysis methodology into its inspection ...
The Drug Supply Chain Security Act (DSCSA) signed into law in November 27, 2013 by president Obama c...
This paper outlines an initial investigation of the bio-pharmaceutical industry (BPI) and the steps...
The availability of quality pharmaceutical products impacts the lives of the global population on a ...
Effective quality risk management is fundamental in guaranteeing the development and manufacture of ...
This paper describes USP-NF compendial updates to six ‘high-priority” excipient monographs: Glycerin...
For several years, quality risk management (QRM) has been such an integral component of healthcare a...
The FDA's Drug Manufacturing Inspection Compliance Program, which constitutes instructions to FDA pe...
AbstractGovernments that procure pharmaceutical products from an Essential Medicine List (EML) bear ...
This project report is submitted in partial fulfilment of the requirements for the degree of Bachelo...
Auditing is a vital function within a pharmaceutical company nowadays. Quality audit is a review and...
There has been an increasing trend in the number of prescribed and over-the-counter drug recall over...
This paper describes USP-NF compendial updates to six ‘high-priority ” excipient monographs: Glyceri...
Background: United States Food and Drug Administration (FDA) is the fastest drug review agency in th...
This research details the FDA\u27s quality systems methodology used in its inspection of biopharmace...
This research describes how the FDA has incorporated risk analysis methodology into its inspection ...
The Drug Supply Chain Security Act (DSCSA) signed into law in November 27, 2013 by president Obama c...
This paper outlines an initial investigation of the bio-pharmaceutical industry (BPI) and the steps...
The availability of quality pharmaceutical products impacts the lives of the global population on a ...
Effective quality risk management is fundamental in guaranteeing the development and manufacture of ...
This paper describes USP-NF compendial updates to six ‘high-priority” excipient monographs: Glycerin...
For several years, quality risk management (QRM) has been such an integral component of healthcare a...
The FDA's Drug Manufacturing Inspection Compliance Program, which constitutes instructions to FDA pe...
AbstractGovernments that procure pharmaceutical products from an Essential Medicine List (EML) bear ...
This project report is submitted in partial fulfilment of the requirements for the degree of Bachelo...
Auditing is a vital function within a pharmaceutical company nowadays. Quality audit is a review and...
There has been an increasing trend in the number of prescribed and over-the-counter drug recall over...
This paper describes USP-NF compendial updates to six ‘high-priority ” excipient monographs: Glyceri...
Background: United States Food and Drug Administration (FDA) is the fastest drug review agency in th...