It is a statutory body constituted under the ‘Rules for the Manufacture, Use /Import /Export and Storage of Hazardous Microorganisms/Genetically Engineering Organisms or Cells, 1989’ notifi ed under the Environment (Protection) Act, 1986.
It was formed as the Genetic Engineering Approval Committee and was renamed to its current name in 2010.
It functions under the Ministry of Environment, Forests & Climate Change (MoEF&CC).
The body regulates the use, manufacture, storage, import, and export of hazardous microorganisms or genetically-engineered organisms and cells in India.
The Committee is chaired by the Special Secretary/Additional Secretary of the MoEF&CC. A representative of the Department of Biotechnology is a co-chair.
The functions of the GEAC are:
It is responsible for the appraisal of activities that involve the large scale use of hazardous microbes and recombinants in research and industrial production from the environment.
It assesses proposals regarding the release of genetically engineered products and organisms into the environment, and this includes experimental fi eld trials as well
It is a statutory body constituted under the ‘Rules for the Manufacture, Use /Import /Export and Storage of Hazardous Microorganisms/Genetically Engineering Organisms or Cells, 1989’ notifi ed under the Environment (Protection) Act, 1986.
It was formed as the Genetic Engineering Approval Committee and was renamed to its current name in 2010.
It functions under the Ministry of Environment, Forests & Climate Change (MoEF&CC).
The body regulates the use, manufacture, storage, import, and export of hazardous microorganisms or genetically-engineered organisms and cells in India.
The Committee is chaired by the Special Secretary/Additional Secretary of the MoEF&CC. A representative of the Department of Biotechnology is a co-chair.
The functions of the GEAC are:
It is responsible for the appraisal of activities that involve the large scale use of hazardous microbes and recombinants in research and industrial production from the environment.
It assesses proposals regarding the release of genetically engineered products and organisms into the environment, and this includes experimental fi eld trials as well
It looks into proposals regarding the use of living modifi ed organism that comes in the risk category III and above in the import/manufacture of recombinant pharma products, or where the end-product of the recombinant pharma product is a modifi ed living organism.
The Committee has the power to take punitive action against people/bodies under the Environment (Protection) Act.
The approval of the GEAC is mandatory before genetically modifi ed organisms and products derived from them can be used commercially.
Genetic Engineering Appraisal Committee (GEAC)