Patent Indicators
1) What Do Patent Indicators Really Measure? Testing Current Theory on Value Drivers of Innovations Within a Structural Two-Stage Discrete Choice Simultaneous Equation Model
Abstract:
Patent indicators are widely used to assess
innovative output. Despite the large variety of empirical studies in
the field, however, the precise meaning of these indicators and their
obvious relation to patent value is still based on assumptions and
intuitions. This paper provides the first empirical test of patent
indicators as value measures in the structural form. It disentangles
the different effects reflected in patent indicators and enhances our
understanding why inventions are valuable at all. Using a newly
assembled data set on European polymer patents, current assumptions on
the innovation incentives set by patentability requirements (novelty,
inventive activity) are tested. The estimations are carried out using a
custom-tailored two stage discrete choice probit model yet unknown in
the literature. The results support the assumptions that novelty and
inventive activity enhance a patent’s value. They confirm the
importance of backward citations, family size,
and forward citations as va lue indicators. However, they expand on and
partly break with the respective explanations why patent indicators
correlate with profitability.
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2) Application of Multiple Known Determinants to Evaluate Legal, Commercial and Technical Value of a Patent
3) Generic Drug Entry Prior to Patent Expiration:
Abstract
Pharmaceutical
drug products have become increasingly important to providing consumers
with a myriad of treatments and cures that increase life expectancy and
enhance lives. It is critical to maintain appropriate incentives for
the development of new drug products, because the necessary research
and development is risky and costly. Innovation in the pharmaceutical
industry, spurred in part by competitive market forces, continues to
bring enormous benefits to Americans.
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Others:
API's and Generic Drugs
To
guide generics companies of all sizes through identification of
potential generic markets, synthesis of the API, development of
formulations and labelling of the finished product, to allow marketing
of a non-infringing product at the earliest possible time after expiry
of the key active ingredient patents".
What is Generic Drug?
When a drug company first invents a drug that
company is the only one allowed to make that drug in the same country
for a certain number of years. After this time period, other companies
are allowed to make the same drug. These drugs are called generic
drugs. The original drug (e.g. Viagra) is called a brand name drug.
rand
name drugs and their generics are IDENTICAL in terms of active
ingredients. The generic pills may look different (because they are
made by a different company) but inside is exactly the same active
ingredient, which works in exactly the same way. The only difference
between brand name drugs and generic drugs is that generics are always
much less expensive. Savings of up to 80% can be made by purchasing
generic drugs instead of namebrand medication.
Are these the same drugs as the name brand products?
Generic
medication and the name brand equivalents are identical. All
pharmaceuticals are simple recipes of common chemical raw ingredients.
Making an exact copy of a pharmaceutical is quite simple. Generics do
not look the same as the brand name products, even though they have the
same active ingredient and work in exactly the same way. In addition,
the same brand name pill may look different if manufacturer in a
different country. For example, Celexa 20MG is a peach colored pill in
the US, yet the Canadian pill is white and a little bit smaller than
the US pill. Both pills are Celexa 20MG, both have the same active
ingredient, and both are made by the same company. But, for whatever
reason, the manufacturer decided to make the Canadian drugs a different
color. When comparing 2 different Generics, they will look different if
they are made by 2 different companies.
Are the Generic Drugs safe?
Generic
drugs are just as safe and effective as their brand-name counterparts.
These are the very companies that manufacture and export in bulk the
drug that goes in to the making of the world's best-selling brands in
US and Europe.
Generic drugs are held to the same rigid standards as the brand name
drug, as dictated by the U.S. Food and Drug Administration. 45% of U.S.
prescriptions today are filled with generic drugs.
CODE OF FEDERAL REGULATIONS [TITLE 21--FOOD AND DRUGS]
CHAPTER I--FOOD AND DRUG ADMINISTRATION,
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of Generic Drugs
The Internet Drug List