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Biosafety Guidelines- In, the ministry of environment and forests (MOEF) promulgated in december, 1989 the rules and procedures for the manufacture, import, use research and GMOs as well as products made from such organisms, this was done under the proviiosn of the environment protection Act, 1986(EPA).

Ant violation and nocompliance, including non reporting of activities, in this area would attract the punitive actions provided under the EPA. In addition, the indian recombinant DNA safet guidelines and regulation have been prepared by and are available on request from recombinant advisory committee (RDAC), Department of Biotechnology (DBT), New Delhi. Field trials using transgenic plants began in 1995.

The DBT implements the research and development experiments utilizing GMOs and recombinant DNA products, while MOEF implements the large scale commercial use of these. the sailent features of these guidelines and Regulations are as follows.

1. Every organisation involved in research and development using recombinant DNA technology is required to set up an institutional biosafety committee (IBC), which has a DBT nominee, IBC is the nodal point for interaction of the organization wit the government.

2. The DBT has a review commitee for genetic manipulation (RCGM), which has all the approvals of on going projects on GMOs and several other issues realted to recominant DNA research and development.

3, each state has, in addition, a state biotechnology coordination committee, and  a district level committee, which are involved in inspection and monitoring of experiments at the field sites.

4. The MOEF has an interministrial committee called the genetic engineering approval committee (GEAC), which has subject specilist as members, and is the competent authority to decide on the large scale use of GMOs.

5. The giodelines recognize four levels of risk in the case of experiments with microorganims, based on pathogenicity of the microorganisms, local prevalence of the concerned disease and of epidemic causing strains in india.

6. experiments  with microorganisms, plants and animals are grouped into the following categories :

(i) Exempt category ( for self cloning experiments)

(ii) category requiring intimation on initiation to competent authority ( experiments involving nonpathogenic DNA vector systems)

(iii) category requiring review and approval by the competent authority ( cloning of genes for toxins , antibiotic resistance , etc)

7. Four different biosafety levels are recognised and containment fecilities for each level are recommended for necessary safeguards

8. Physical Containment envisages to limits the spread of dangerous micororganisms by

(i) Good laboratory practices

(ii)safety equipment and

(iii) laboratory design and facilities

9.Biological containment consists of the use of vector and hosts in such a way so that it

(i) can limit the infectivity of vector to specific hosts, and

(ii) control host vector survival in the environment