Initiating laws to regulate biotechnology essay

The key factors to be considered in these legal documents include; area of specialization, the time line for implementation, how the innovation is going to benefit the society, state and the global village. Pan Soll Press Berg, Amazon. For instance in this era of numerous HIV infections, malformed genes, problems in fertilizations and conception, and myocardial regenerations.

Challenges in regulating biotechnology

The principle of a gene bank is that the dehydrated seeds can retain their viability for a longer period of time if stored in cold conditions.

Rather, it reflected a position that biotechnology could be adequately regulated through the existing federal infrastructure and by adapting existing laws to new technologies.


Using genetic engineering techniques, it has become possible to obtain the mutants of microorganisms which can produce a much higher amount of product of interest than the natural ones. The discussion focuses first on the USDA, then the EPA and then the FDA, as this represents the order in which a person developing a new agricultural biotechnology product might commonly encounter each of these agencies.

Some of these centres are: These two strategies are given below: Researchers often conduct off-season greenhouse testing in order to expedite data collection.

The environmental impact statement must examine the likely effects of the project in more detail and identify potential alternatives to the project. A genetic counsellor may also prescribe gene therapy to the patients if he finds any scope for it after diagnosis.

This strategy of correcting the diseases is termed as gene therapy.

A race resistant to infections or any other forms of gene multination and is capable of achieving the highest rates of life expectancy. In order to obtain registration, a new pesticide must not cause "unreasonable adverse effects on the environment" 7 USC.

The Environmental Protection Agency has utilized the Toxic Substances Control Act as its legal authority to promulgate regulations for genetically engineered microorganisms 40 C.

Along with conserving the original genetic diversity, gene banks also make the genetic material available as raw material to the breeders and biotechnologists. Biotechnology—the use of biological knowledge and materials for human benefit—has been used for thousands of years in agriculture and medicine.

In this voluntary consultation process, the Food and Drug Administration requests that firms provide a summary of their food or feed safety and nutritional assessment to the agency and discuss these results with Food and Drug Administration scientists prior to beginning commercial distribution.

For example, if the genetically engineered food contained a significantly different nutritional profile than its conventional counterpart, labeling to that effect might be required.

Proponents of the FDA biotechnology policy claim that the policy has been a success. In response to widespread objections from scientists to use of the term "plant-pesticides," the new regulations renamed pesticidal substances which had been genetically engineered into plants as "plant-incorporated protectants.

The firm that will be able to achieve a perfect innovation therapy for HIV patients will go on the scientist books of records. Further in vitro fertilizations helps in assisted reproductive technology for animals as well as few human beings having related problems.

For copyright reasons some linked items are only available to members of Parliament. Biotechnological approaches are applied to accomplish goals for the benefit of mankind.

Use of any of these "plant pests" to make a transgenic plant makes that plant a "regulated article. The person who serves the genetic counselling to the couples is called as a genetic counsellor.

Available on the World Wide Web: FDA to strengthen pre-market review of bioengineered foods. The Center for Veterinary Medicine considered the additions of rBST or the genetic modifications involved in producing rBST to constitute the addition of an animal drug, making the product subject to its pre-market approval authority.

This approach is being used for trials made to treat cancer and blood disorders mainly. The Food and Drug Administration also normally prepares an environmental assessment when it approves a new drug.

Types of Gene Therapy: So, the gene therapy may be defined as the introduction of normal functional gene in the defective cells of a patient to correct a genetic or acquired disorder.Links to biotechnology guidance documents & regulatory information. Draft Guidance for Industry: Voluntary Labeling Indicating Whether Food Has or Has Not Been Derived From Genetically Engineered.

Initiating Laws to Regulate Biotechnology Essay Sample

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Essay on Biotechnology: Definition, Advancement and Application

Biotechnology and Intellectual Property Rights. BIOTECHNOLOGY POLICY-MAKING, REGULATIONS AND DEVELOPMENT IN THE ASEAN REGION Banpot Napompeth Founder &. Initiating Laws to Regulate Biotechnology Essay Sample Biotechnology is in people’s heart and many people wants to see it happen.

The federal policy that no new laws were needed to regulate the products of biotechnology was first adopted in by the federal regulatory agencies in the Coordinated Framework for Regulation of Biotechnology.

The Environmental Protection Agency's use of TSCA to regulate bio-engineered plants as "chemical substances" is one example of how federal agencies are attempting to adapt pre-existing laws to regulate new technologies in ways that could not have been foreseen when the laws were first enacted.

Initiating laws to regulate biotechnology essay
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