 "Govt continues to allow 100% FDI in existing pharma firms")
New Delhi: Government today decided to retain the policy of allowing 100 percent foreign investment in the existing pharma firms, brushing aside concerns about non-availability of affordable drugs in view of MNCs takeovers.
The Department of Industrial Policy and Promotion (DIPP) said however that as far as the contentious issue of non-compete clause is concerned, the Foreign Investment Promotion Board (FIPB) will take a view on it on case-by-case basis.
[caption id=“attachment_1295427” align=“alignleft” width=“380”]  Representational image. Reuters[/caption]
“The government has reviewed the position in this regard and decided that the existing policy would continue with the condition that ’non-compete’ clause would not be allowed except in special circumstances with the approval of the FIPB,” the DIPP said in a Press Note.
Faced with a rush of multinationals (MNCs) acquiring Indian pharma firms, the DIPP had earlier proposed stringent norms to tighten the Foreign Direct Investment (FDI) policy for the sector.
It had said the continuous acquisition of Indian pharma companies will severely impact availability and affordability of generic medicines in the country, and asked for a reductionin the FDI cap to 49 percent from 100 percent in rare or critical pharma verticals.
However, the Union Cabinet at its meeting dismissed the DIPP concerns.
In September, the government cleared the Rs 5,168-crore deal of the US-based Mylan Inc for acquiring Bangalore-based pharma firm Agila Specialties, a subsidiary of Strides Arcolab.
Impact Shorts
More ShortsIn 2008, Japanese firm Daiichi Sankyo had bought out the country’s largest drug maker Ranbaxy for USD 4.6 billion.
US-based Abbot Laboratories had acquired Piramal Health Care’s domestic business for USD 3.7 billion.
DIPP had said that over 96 percent of the total FDI in the sector between April 2012 and April 2013 has come into the brownfield pharma, or existing projects and companies.
India permits 100 percent FDI in pharma through automatic approval route in the greenfield, or new projects.
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