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CDSCO Mandates Pharma Companies to Maintain Adverse Event Reporting Systems

  • Post published:September 1, 2026
  • Post category:Knowledge

In June 2026, India's Central Drugs Standard Control Organisation (CDSCO) issued a directive requiring all pharmaceutical manufacturers in India to maintain a robust pharmacovigilance system for reporting adverse events (AEs)…

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India’s Pharma Ambitions Meet Regulatory Capacity: What Buyers Should Know

  • Post published:August 30, 2026
  • Post category:Knowledge

India has set ambitious goals for its pharmaceutical sector: becoming the "pharmacy of the world" for generic medicines, expanding into complex generics and biosimilars, and boosting exports to $50 billion…

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Understanding India’s Drug Safety Framework: A 2026 Buyer’s Guide

  • Post published:August 28, 2026
  • Post category:Knowledge

India's pharmaceutical regulatory framework has undergone significant transformation in recent years, with the Central Drugs Standard Control Organisation (CDSCO) and the Pharmacovigilance Programme of India (PvPI) playing increasingly active roles…

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CDSCO Bans Injectable Drugs for Cosmetic Use: What Indian Consumers Should Know

  • Post published:August 26, 2026
  • Post category:Knowledge

On May 21, 2026, India's Central Drugs Standard Control Organisation (CDSCO) issued a clear directive: no injectable product can be classified or sold as a cosmetic. The directive, reported by…

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Recent Posts

  • Understanding CDSCO’s NSQ Drug Quality Alerts: A Buyer’s Guide for 2026
  • CDSCO’s Risk-Based Regulation Push at iPHEX 2026
  • A Buyer’s Guide to WHO-GMP Certified Indian Generic Medicines
  • India’s PLI Bulk Drug Push: Rs 5,210 Crore Invested by June 2026
  • CDSCO’s Digital Drug Regulatory Platform: What Buyers Should Know

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