ONE 2 ONE, written by Steve Murrell, discusses in simple language the basic yet fundamental foundations of following Jesus. It is meant to be shared i …
Good manufacturing practice (GMP) is the key part of the quality assurance for medicines in the European Economic Area (EEA). EU-GMP is to ensure that …
Good manufacturing practice (GMP) is the key part of the quality assurance for medicines in the European Economic Area (EEA). The manufacture of steri …
Recalled! retrieves all Recalls, Recall Alerts and Press Releases from the US Consumer Product Safety Commission (CPSC) and Recalls and Safety Alerts …
In US, current Federal law requires that a drug be the subject of an approved marketing application before it is transported or distributed across sta …
The various acts enforced by FDA require an adequate showing of product safety prior to introduction into the marketplace. In order to ensure adequate …
The Biologics License Application (BLA) is a request for permission to introduce, or deliver for introduction, a biologic product into interstate comm …
Premarket Approval (PMA) is the most stringent type of device marketing application required by FDA. PMA regulates most Class III medical device. A PM …
The ICH Q10 - Pharmaceutical Quality System is a harmonized Guideline in USA, Europe and Japan and was approved in 2008. This Guideline applies to pha …