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    <title>Press Note No. 2 (2015 Series) - Review of the policy on Foreign Direct Investment (FDI) in Pharmaceutical Sector- carve out for medical devices</title>
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    <description>Revision permits full automatic FDI for manufacturing of medical devices, exempting those projects from the pharmaceutical FDI conditions such as non-compete restrictions, certificate requirements with FIPB applications, and possible brownfield conditions. The press note defines &quot;medical device&quot; to include instruments, apparatus, appliances, implants, materials, software and accessories for diagnostic, therapeutic, monitoring, investigational, life-support and in vitro diagnostic purposes, and states the definition is subject to amendment under the Drugs and Cosmetics Act.</description>
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