Environmental Monitoring
Your Guide to Pharmaceutical Validation & 6 Principles for Effective Implementation
In good manufacturing practice (GMP) and other GxP’s, the term validation has a formal, specific meaning. In this context, validation is a quality management tool used to confirm that a process or a piece of equipment satisfies its intended purpose through the use of objective data. In highly regulated industries like pharmaceuticals, validation is used…
Read MoreWhy Is Temperature Mapping in Pharma Important?
A growing trend in the pharmaceutical industry is the development of more complex and fragile products, like biologicals, chemical mixtures, and large molecules (COVID-19 vaccines are an example of this trend). These products generally must follow a standard operating procedure (SOP) that requires more stringent temperature controls to prevent them from degrading or deactivating during…
Read MoreUnderstanding Pharmacy Temperature Requirements for Medication Storage
If vaccine and pharmacy medication storage reaches the wrong temperature, several things can happen – rendering them less effective than intended or even chemically altered, causing inadvertent patient harm. Because of this risk, strict pharmacy temperature requirements have been put into place to ensure medications are manufactured, transported, and stored properly before they reach the…
Read MoreEnhancing DicksonOne, Floor Plan and Custom Dashboards
Discover how DicksonOne’s new features, including floorplan and Dashboard, are revolutionizing environmental monitoring.
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