Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements (Oct 7, 2025)" training has been added to ResearchAndMarkets.com's ...

A quality control department of a pharma industry carries out sampling (raw materials, finished products, etc) following established procedures and analyzes it in the QC laboratory. In the earlier GLP ...

Data integrity is a major concern in the regulated pharmaceutical industry due to discovery of either poor record management practices or falsification of data. This has resulted in numerous FDA ...

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 ...

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 ...

Dublin, Jan. 30, 2025 (GLOBE NEWSWIRE) -- The "Data Integrity Auditor Masterclass Training Course" conference has been added to ResearchAndMarkets.com's offering. Data integrity has received more ...

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 US Food and Drug Administration (FDA) on Wednesday finalized its questions and answers guidance on complying with data integrity requirements under current good ...