With regulatory agencies like the FDA, EMA, and MHRA intensifying data integrity compliance, significant market opportunities exist in providing robust data management solutions. Organizations can ...

Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...

While data integrity failures within health IT systems only ranked fourth on the ECRI Institute's list of top healthcare technology hazards published last fall, when it comes to patient safety ...

EMA's work plan emphasizes supply chain integrity, product quality, and new manufacturing technologies' impact on the supply chain. Revised GMP guidelines include updates to documentation, digital ...

Laboratories operating under GMP or GLP regulations must follow guidelines set by agencies to protect scientific integrity or demonstrate quality assurance of manufactured products. Regulated labs ...

India has advantage over China because Indian pharma industry has more pharmacy personnel than China. Indian Pharma Industry needs to protect its brand image as quality manufacturer by learning to ...

The ECRI Institute has released its first annual list of the top 10 patient safety concerns for hospitals and health systems based on analysis of more than 30,000 patient safety incidents and other ...