A: No new regulations were published in 2025 specific to data integrity. The evolving global regulatory systems do, however, ...
The USFDA further highlighted deficiencies in environmental monitoring in manufacturing areas, indicating gaps in ensuring ...
Built-in data integrity is a bare minimum requirement in today’s BioPharmaceutical manufacturing. Good Manufacturing Practices (GMP) regulations of the Food and Drug Administration (FDA) highlight the ...
Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...
4dOpinion
AI in pharma sector
While AI has already made inroads into drug discovery and clinical research, its most profound impact may be in quality ...
The pharmaceutical industry is undergoing a seismic transformation, driven by the integration of data science and analytics. As the demand for novel therapies and personalized medicine surges, leaders ...
The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech (Dec 9th - Dec 10th, 2025)" training has been added to ResearchAndMarkets.com's offering.
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