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Uncovering the Hidden Insights in Clinical Trial Documents: Critical Steps to Intelligent Document Processing

MedCity News

In clinical trials, pharmaceutical companies are seeking to optimize operations and improve efficiency by automating and enhancing processes through Artificial Intelligence (AI) and Machine Learning (ML). One area where this can reap tangible benefits across clinical trials is in data processing.

Safety 113
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The role of GAMP 5, data integrity and QbD in pharmaceutical quality assurance

European Pharmaceutical Review

Researchers have described the impact of data integrity, GAMP 5 and quality by design (QbD) principles on pharmaceutical quality assurance (QA) , highlighting the importance of data integrity through various case studies. Data integrity guarantees the reliability of data collected throughout various stages of drug development.”

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Regulatory revision essential for bioprocess IIoT adoption

European Pharmaceutical Review

As a system that uses various technologies , such as data analytics and artificial intelligence (AI), to transfer data between each other autonomously in an industrial setting, IIoT “enables wide-scope data collection and utilisation, and reduces errors, increases efficiency, and provides an improved understanding of the process in return”.

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Transforming pharmaceutical manufacturing: The AI revolution

European Pharmaceutical Review

Integrative Analysis of Multi-Omics Data with Deep Learning: Challenges and Opportunities in Bioinformatics. With the added benefit of Internet-of-Things (IoT)-enabled real-time monitoring, AI can maintain constant compliance with stringent quality standards that tends to data integrity.

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Can automated buffer management systems overcome bioprocessing bottlenecks?

European Pharmaceutical Review

A new automated buffer management system (BMS) that includes buffer volume monitoring, automatic ordering, preparation and delivery of buffers to the buffer-consuming purification systems has been developed by Swedish researchers. Neither is a system able to handle automatic orders without operator intervention. Isaksson et al.

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10 Ways AI/ML Technologies Can Enhance Software Quality in the Life Sciences Industry

PM360

As pharmaceutical regulations increasingly intersect with software development standards, the traditional approach to Computer System Verification (CSV) is falling short. If a misinterpretation exists between engineers and testers on the solution developed, then such requirements will have higher risks on the entire lifecycle.

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Elevating pharmaceutical manufacturing processes with real-time insights

European Pharmaceutical Review

The race to develop new drugs and therapies demands rapid drug discovery, testing and time-to-market. This is a systematic approach that harnesses the power of data and leverages real-time analysis tools to closely monitor and control critical process parameters (CPPs) and their relationship with critical quality attributes (CQAs).