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Draft Pharma Policy

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August 24, 2017

Why in news?

The draft pharma policy was recently released by the Department of Pharmaceuticals (DOP).

What are the highlights of draft pharmaceutical policy?

  • The new pharmaceutical policy proposes to balance the need for price control over medicines.
  • Union government will gain a greater role in deciding prices of medicines and medical devices.
  • Pricing authority will regulate only medicines that are specified by the government in the National List of Essential Medicines.
  • The price caps being imposed on patented medicines are reduced.
  • Policy allows pharmaceutical manufacturers to sell their medicines under only under generic names and not under differently-priced brands.
  • Manufacturing of drugs under WHO standards is made mandatory.
  • The policy seeks to bring down the unreasonable trade margins offered by various stockists to hospitals.

What are the issues with the policy?

  • The policy fails to lay controls over the chemists, this may facilitates the sale of fake drugs.
  • The policy doesn’t have any mechanisms to boost production standards.
  • Instead of an appellate authority, it seeks to give bureaucrats more powers on drug controls.
  • Direct price control – Government takes role of fixing the drug price.
  • This will affects the quality, innovation, and hurts patients as much as it does companies.
  • It opens the door to lobbying and rent-seeking with all the attendant dangers for competition and for corruption.

What measures can be taken?

  • It will be better if price monitoring focuses on essential drugs, there are about 200.
  • Strict price control measures needs to be avoided and market friendly pricing should be followed.
  • Domestic production of import drugs should be promoted, with better quality and affordability.
  • The government should also consider specific steps against overcharging of prices by the industries.

 

Source: Business Standard

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