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Pharmacopoeia Commission for Indian Medicine
Source : PIB

GS II : Governance

What is discussed?

  1. About the Commission
  2. How it helps ?

Why in News ?

The Government of India has established Pharmacopoeia Commission for Indian Medicine & Homoeopathy (PCIM&H) as a subordinate office under Ministry of Ayush by merging Pharmacopoeia Commission of Indian Medicine & Homoeopathy (PCIM&H) and the two central laboratories namely

  1. Pharmacopoeia Laboratory for Indian Medicine (PLIM), Ghaziabad
  2. Homoeopathic Pharmacopoeia Laboratory (HPL) 
Key Facts

Pharmacopoeia Commission for Indian Medicine & Homoeopathy (PCIM&H)

  • The Commission is engaged in development of Pharmacopoial Standards for Ayurvedic, Unani, Siddha & Homoeopathic drugs.

    Pharmacopoeia Commission for Indian Medicine
    Image by Bruno /Germany from Pixabay
  • Also acting as Central Drug Testing cum Appellate Laboratory for Indian systems of Medicine & Homoeopathy.
  • Pharmacopoeia is an officially recognized book of standards as per the Drugs and Cosmetics Act, 1940 and Rules 1945 there under.
  • As per the Second Schedule of the Drugs and Cosmetics Act, it is designated as the official book of standards for drugs imported and/or manufactured for sale, stock or exhibition for sale or distribution in India.
  • It specifies the standards of drugs manufactured and marketed in India in terms of their identity, purity and strength.

How this merger Helps?

  • This will enhance the infrastructural facilities, technical manpower and financial resources these organisation.
  • It will facilitate focused and cohesive development of standards of AYUSH drugs and publication of pharmacopoeias and formularies.

Current Status 

  • After re-establishment, a total of 1483 samples of ASU&H drugs have been tested during 6th July, 2020 to till date and 03 Pharmacopoeial monographs along with their formulary specifications for AYUSH Kwath related formulation has been published.
  • Apart from Pharmacopoeial Monographs, National Formulary for Unani Medicines, Part-IV (2nd Edition) comprising formulary specifications of 166 formulations have also be published.

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