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  1. Navigating Biosimilar Regulatory Pathways in Emerging Markets: Insights from BRICS Nations
  2. The Current Regulatory Environment for Software Used in Medical Devices: A Need for Refined International Strategies
  3. Managing indian pharmaceutical supply chain.
  4. Regulatory Procedures and Integrated Requirements for Early Phase Development of a Pharmaceutical Drug Product
  5. A Critical Appraisal on Controlled Drugs: Classification, Global Regulatory Provisions, and Distribution