Food, Farma and Healthcare

Legal Eye has immense expertise and experience in the area of Food and Pharma/ Drug Laws. Legal Eye has in-depth knowledge and understanding of the legal and regulatory framework relating to drugs and pharmaceutical legislations including prevention of food adulteration legislation.
Legal Eye advises on introduction, import and marketing of Generic and New Drugs including bulk drugs in the Indian market. Further, Legal Eye advises on legal and regulatory issues relating to clinical trials (phases 1, 2 and 3), post marketing survey and various issues relating to indemnity and insurance of subjects/ patients. Legal Eye has capabilities to advise and opine on various issues arising out of international treaties such as Declaration of Helsinki, Good Clinical Practice guidelines and the Agreement on Trade Related Aspects of Intellectual Property Rights especially Article 39.3 concerning interpretation of data exclusivity/ protection.
Legal Eye advises and provides legal assistance in the following matters:

  • Agreements relating to manufacturing, marketing, import, sponsorship, etc.
  • Clinical Trials
  • Regulatory Approvals from Drug Controller General
  • Food Adulteration
  • Labelling and packaging guidelines
  • Foreign Direct Investment
  • Tax Advice
  • Intellectual Property protection and registration such as Patents, Trademarks etc.