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Chapter 10 Regulatory affairs and compliance in the pharmaceutical sector

  • Rishabha Malviya , Shristy Verma , Sonali Sundram und Harshil Shah
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Abstract

The pharmaceutical sector is accountable for guaranteeing the safety, efficacy, and quality of therapeutic products. Attaining worldwide competitiveness in pharmaceutical manufacturing requires rigorous adherence to ongoing quality, environmental protection, occupational health, and safety standards. The study analyzes the recommendations and effective implementation strategies of the United States Food and Drug Administration. The objective of the chapter is to deliver an exhaustive overview of US regulatory compliance, emphasizing US FDA rules. Artificial intelligence (AI) is an advanced technical instrument that is significantly transforming several GMP sectors. AI systems can understand complex regulatory documents, therefore aiding pharmaceutical companies in staying abreast of the continually evolving compliance demands for medication research and approval. The application of AI extends to crucial areas such as compliance with packaging and labeling, significantly improving the efficiency and accuracy of regulatory affairs.

Abstract

The pharmaceutical sector is accountable for guaranteeing the safety, efficacy, and quality of therapeutic products. Attaining worldwide competitiveness in pharmaceutical manufacturing requires rigorous adherence to ongoing quality, environmental protection, occupational health, and safety standards. The study analyzes the recommendations and effective implementation strategies of the United States Food and Drug Administration. The objective of the chapter is to deliver an exhaustive overview of US regulatory compliance, emphasizing US FDA rules. Artificial intelligence (AI) is an advanced technical instrument that is significantly transforming several GMP sectors. AI systems can understand complex regulatory documents, therefore aiding pharmaceutical companies in staying abreast of the continually evolving compliance demands for medication research and approval. The application of AI extends to crucial areas such as compliance with packaging and labeling, significantly improving the efficiency and accuracy of regulatory affairs.

Heruntergeladen am 23.12.2025 von https://www.degruyterbrill.com/document/doi/10.1515/9783111574288-010/html?lang=de
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