--Definition of
IP(Intellectual Property) and IPR(Intellectual Property Rights)
·
The issues related to legal characterization and the treatment of
trade related biotechnological processes and products
·
These are popularly
known as Intellectual Property.
·
Intellectual Property includes
1.Patents
2.
trade secrets
3.
copyrights
4.trademarks.
·
In biotechnology, the intellectual property
covers the processes and products which result from the development of genetic
engineering techniques through the use of restriction enzymes to create
recombinant DNA.
·
Restriction enzymes (is just like a scissor which) cuts
the desired gene of a virus (WHICH WE
WANT TO PUT IN THE HOST CELL OR MOTHER DNA) and sticks it with the help
of ligase
enzyme (which is like fevicol)onto
the mother DNA.In this way we get the Recombinant DNA with the desired traits.
--- Advantages
of getting a patent
1.help in encouraging and safeguarding intellectual and artistic creations.(No Piracy to your innovations)
2.todisseminate new ideas and technologies quickly and widely.
3. promote investment.
4.They help the inventor to provide the fruits and benefits of his creation and invention to the public.
5. They provide increased opportunities for the distribution of the above effects across countries in a manner proportionate to national levels of economic and industrial development (OECD, Paris, 1989)
-----What
are breeder’s right?(PBR)
·
The new crop varieties are developed and
protected through “plant breeder’s rights or PBRs. The PBRs ensures that the plant breeder whodeveloped a particular variety gets the
exclusive rights for marketing the variety.
·
The following two major steps were taken in consideration
of PBRs:
1. The Food and Agriculture Organisation (FAO) has an International treaty on plant genetic resources for food and agriculture. This treaty consists of a particular clauses which refers to operation of farmer’s rights.
2.The ‘Plant Varietal Protection and Farmer’s Rights Act 2001 agrees for the right of farmers, breeders, and researchers. The protection is provided by making compulsory licensing of rights, and inhibiting the import of plant varieties consisting of ‘genetic use of restriction technology’ (GURT) e.g. terminator technology of Monsanto.
1. The Food and Agriculture Organisation (FAO) has an International treaty on plant genetic resources for food and agriculture. This treaty consists of a particular clauses which refers to operation of farmer’s rights.
2.The ‘Plant Varietal Protection and Farmer’s Rights Act 2001 agrees for the right of farmers, breeders, and researchers. The protection is provided by making compulsory licensing of rights, and inhibiting the import of plant varieties consisting of ‘genetic use of restriction technology’ (GURT) e.g. terminator technology of Monsanto.
·
Following conditions should be fulfilled to
grant protection to the new varieties:
a) the new variety must always be new i.e. it should not have ever been exploited commercially.
b) It should be biologically distinct and possess different characters.
c) The new variety of the plant must have uniform characters.
f) The distinguishing character of new variety must be stable for generations.
g) The new variety should have taxonomic validity i.e. systematic position, generic and species names etc.
a) the new variety must always be new i.e. it should not have ever been exploited commercially.
b) It should be biologically distinct and possess different characters.
c) The new variety of the plant must have uniform characters.
f) The distinguishing character of new variety must be stable for generations.
g) The new variety should have taxonomic validity i.e. systematic position, generic and species names etc.
-- The
general layout of a patent
·
A patent consists of
three parts: the grant, specifications, and claims.(SCG
or Syndey Cricket Ground just a mnemonic)
·
The Grant- The grant is filled at the patent office which is not published.
It is the actual signed document which is the agreement that grants patent
rights to the inventor.
Specifications- The specifications part is narrative and describes the subject matter and explains about the process of invention. It is published as a single document which is made public at a minimum charge from the patent office.
The claim- The claim section specifically defines the scope of the invention to be protected by the patent to which the others may not practice.
Specifications- The specifications part is narrative and describes the subject matter and explains about the process of invention. It is published as a single document which is made public at a minimum charge from the patent office.
The claim- The claim section specifically defines the scope of the invention to be protected by the patent to which the others may not practice.
·
Reading a Patent
·
In order to file a
patent, the documents required should have a specialized structure. An applicant should first file a patent
in his or her own country and then at a later stage/date files in the
international office. The application is prepared with a specific, clear and concise title. A patent attorney is
appointed for the legal aspects of the patent whose job also involves filling
the patent in the office of the Controller of Patents.
(a) WIPO- World Intellectual Property
Organisation,
(b)TRIPS- Trade related Intellectual Property
rights,
(c) GM-
Genetically modified,
(d) PCT-
Patent Co-operation Treaty,
(e) GURT-
Genetic use restriction technology.
---What
do you mean by patenting live forms and examples
·
The EPO has suggested to
patent the genetically engineered liveforms.
·
“Onco
mouse” is one of the examples
of which initially the patent claims was rejected but on appeal the previous
decision was overruled.
·
Genetically engineered E.coli, in which human genes
for insulin, growth hormone, t-PA etc have been introduced, have been patented
in the USA.
·
The transgenic herbicide and bollworm resistant
cotton, and insect- resistant tobacco have been granted patents.
·
Several countries such
as Japan, USA, Europe, etc. have modified the patent laws stating that the
transgenic plants and animals can be protected through patent claims.
----
Trade secrets and Trademarks
·
Trade secrets relate to
private proprietary information or physical material that allows an advantage
to the owner. Trade secrets in the biotechnology field includes
materials like hybridization conditions, cell lines, corporate merchandise
plans, customer lists etc. It is sometimes difficult to maintain trade
secrets in biotechnology due to its large degree of research component.
If the trade secrets become public before the granted period, the intellectual is paid compensation and unauthorized users are punished by the Court.
If the trade secrets become public before the granted period, the intellectual is paid compensation and unauthorized users are punished by the Court.
·
The
Trademark relates to distinctive
words or symbols applied to products or services by manufacturers and helps to
distinguish the goods of different companies. In biotechnology, the laboratory
equipments, and some of the vectors useful in recombinant research are known by
their trademarks. The public makes use of these trade works in order to choose
whose goods they will have to buy. Trademark laws vary in every country and
through agreement it is ensured that the trademark of one country must be
protected in another country.
---- Main
areas of consideration for safety aspects in biotechnology
The main areas of consideration for safety
aspects in biotechnology are the following:
1.How to dispose off spent microbial biomass and purify the effluents from biotechnological processes?
2.The toxicity of the allergy associated with microbial production.
3. How to deal with the increase in the number of antibiotic resistant pathogenic microorganisms?
4. How to evaluate the pathogenicity of the genetically engineered microorganisms to infect humans, plants and animals?
1.How to dispose off spent microbial biomass and purify the effluents from biotechnological processes?
2.The toxicity of the allergy associated with microbial production.
3. How to deal with the increase in the number of antibiotic resistant pathogenic microorganisms?
4. How to evaluate the pathogenicity of the genetically engineered microorganisms to infect humans, plants and animals?
-- PCT
and Budapest treaty.
·
The “Patent Co-operation Treaty”(PCT) was signed in 1970 and is administered
by the World Intellectual Property
Organization (WIPO) based in Geneva.
·
Patent applications filed
under PCTs are first processed by WIPO before being formally introduced into
designated national systems.
·
The patents granted by PCT are treated as
International patent.
·
The patent applications are processed by the
WIPO which processes the patent application in an “International phase”.
·
The international phase has concerns with: (a) formal preliminaries, (b) art
search, (c) publication of patent application.
·
The
Budapest Treaty (1980)
provides for the recognition of culture collections at International Depository
Authorities (IDA), in any of which a new
strain of microorganism can be deposited for the purposes of a patent
application in any member state.
·
The strains which can serve the purpose of
scientific community or society are accepted.
·
These can be procured if required in future to
work in Industry or research. The strains which are deposited are allocated an
accession number, accession date, source of isolation and specific function.
·
The purpose of convention of Budapest Treaty was
to provide International Recognition of Microorganisms’ for the purpose of
patent procedure.
--What
is the role of copyright in biotechnology?
·
The copyright protection
is only a form of expression of ideas.
·
The patents and trade
secrets provide protection of only
basic know how, whereas copyrights protect the expressed materials viz.
materials in printed, video-recorded r taped form. In the field of
biotechnology, copyright usually may cover DNA sequence data which may be
published.
·
Computer data bases,
photomicrographs of DNA instruction manuals can also be copyrighted.
WRITTEN BY -GEORGE SINHA
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