Compliance with good manufacturing or laboratory practice (GMP or GLP) guidelines can help labs ensure the quality and integrity of biopharmaceutical data. Poor data management or deliberate ...
Strengthen information governance with clear policies for data classification, retention, and legal holds to meet industry regulations and ensure defensibility. Embed compliance and collaboration ...
Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...
Remco Munnik, Arcana, details pharma's shift to data-first operations, AI adoption, and robust data stewardship. PharmTech recently spoke with Remco Munnik, founder and owner, Arcana Life Sciences, to ...
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.
AI emerged as a key differentiator in accelerating development timelines and enhancing clinical operations. Decentralized trial infrastructure and real-world data integration unlocked new operational ...
The Cybersecurity Imperative for Indian Pharma Manufacturing in 2025 India’s pharmaceutical manufacturing sector is a cornerstone of global healthcare. As the world’s largest supplier of generic ...
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