CDSCO Waives Local Clinical Trials for new drugs approved in developed countries | Current Affairs | Vision IAS
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Waiver has been granted under Rule 101 of New Drugs and Clinical Trials Rules, 2019, which allows Drugs Controller General of India (DCGI aka Central Licencing Authority) to specify certain countries for considering waiver of local clinical trials for approval of new drugs.

  • Now countries like USA, UK, Japan, Australia, Canada, and EU can supply drugs to India without requiring local trials. 
    • Waiver covers five categories: Orphan drugs for rare diseases; Gene and cellular therapy products; New drugs used in pandemic situations; New drugs for special defense purposes; and New drugs having significant therapeutic advances over current standard of care.
      • Orphan drug means a drug intended to treat a condition which affects not more than 5 lakh persons in India.
  • However, final phase four clinical trials for these drugs will still be mandatory.
  • DCGI (head of CDSCO) is final regulatory authority for approval of clinical trials in country.

Significance of Current Waiver

  • Ensure availability of latest medicines to treat diseases like cancer, rare and autoimmune disease, etc. 
  • Reduce costs of public procurement by governments under various schemes like Ayushman Bharat etc.
  • Reduce cost incurred by pharmaceutical companies in conducting local trials.

About Central Drugs Standard Control Organisation (CDSCO)

  • CDSCO under Ministry of Health & Family Welfare is National Regulatory Authority of India.
  • Under Drugs and Cosmetics Act 1940, CDSCO is responsible for approval of Drugs, Conduct of Clinical Trials, laying down the standards for Drugs, etc.
  • Four phases of Clinical Trials
    • Phase I: Small group of volunteers to evaluate drug’s safe dosage range and identify side effects.
    • Phase II: Drug given to larger group (100 to 300), including patients with particular disease to see its effectiveness.
    • Phase III: Drug given to large groups (1,000 to 3,000), including patients to compare it to other commonly used treatments, etc.  
    • Phase IV: Drug/Treatment has been approved by DCGI and marketed for public use. 
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