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Ensuring Regulatory Compliance in Pharmaceutical Supply Chains: Strategies for New Drug Introductions

EasyChair Preprint no. 13668

13 pagesDate: June 15, 2024


Ensuring regulatory compliance in pharmaceutical supply chains is critical, especially when introducing new drugs to the market. This article delves into the complexities and strategies involved in maintaining compliance throughout the pharmaceutical supply chain. It covers the regulatory landscape, the drug introduction process, risk management, technology and automation, data integrity, staff training, third-party management, and future trends. Through detailed examination and case studies, this comprehensive guide aims to provide pharmaceutical companies with the knowledge and tools necessary to navigate the regulatory landscape effectively, ensuring the successful and compliant introduction of new drugs.

Keyphrases: Artificial Intelligence in Compliance, Automation in Manufacturing, Blockchain for Traceability, clinical trials, Compliance Training Programs, Data Integrity, Digital Transformation, Good Distribution Practices (GDP), Good Manufacturing Practices (GMP), New Drug Introductions, pharmaceutical supply chain, Pharmacovigilance, Post-Approval Obligations, Quality Management Systems (QMS), Regulatory Compliance, risk management, Supplier Qualification, Supply Chain Security, Sustainable Practices in Pharmaceuticals, Technology in Pharmaceuticals

BibTeX entry
BibTeX does not have the right entry for preprints. This is a hack for producing the correct reference:
  author = {Olawale Ajala},
  title = {Ensuring Regulatory Compliance in Pharmaceutical Supply Chains: Strategies for New Drug Introductions},
  howpublished = {EasyChair Preprint no. 13668},

  year = {EasyChair, 2024}}
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