Add to ORKGThe article deals with problem of choice in the administration of brands and generics, a review of the literature on the bioequivalence of these drugs is provided
The concept of: Generic drugs and patented drugs vs. brand name drugs and non-proprietary (generic) ...
Patents for several blockbuster biological products are expected to expire soon. The Food and Drug A...
The Author(s) 2015. This article is published with open access at Springerlink.com A generic medicin...
The article discusses the factors that influence the efficacy and safety of generic drugs, including...
A generic drug is a product that is comparable to brand/reference listed drug product in dosage form...
Current regulation for generic approval is based on the assessment of average bioequivalence. As ind...
AbstractPolicymakers tend to focus on improving patented drug policies because they are under pressu...
Generic drugs are used by millions of patients for economic reasons, so their evaluation must be hig...
Generic drugs are copies of brand-name drugs that have exactly the same dosage, intended use, effect...
R educing health costs is a hot political issue in manycountries, so the introduction and use of gen...
BACKGROUND AND OBJECTIVES: Generic substitution has become a common practice since the late 1970s in...
This review article discusses the similarities and differences in the research, production and use i...
peer reviewedComplementarily to a previous publication, this paper tries to answer a few commonly as...
Generic drugs are medicines which are identical, or are bioequivalent to brand name drugs in dosage,...
In the last one decade, due to expiry of patented products as well as their exclusivity period, a dr...
The concept of: Generic drugs and patented drugs vs. brand name drugs and non-proprietary (generic) ...
Patents for several blockbuster biological products are expected to expire soon. The Food and Drug A...
The Author(s) 2015. This article is published with open access at Springerlink.com A generic medicin...
The article discusses the factors that influence the efficacy and safety of generic drugs, including...
A generic drug is a product that is comparable to brand/reference listed drug product in dosage form...
Current regulation for generic approval is based on the assessment of average bioequivalence. As ind...
AbstractPolicymakers tend to focus on improving patented drug policies because they are under pressu...
Generic drugs are used by millions of patients for economic reasons, so their evaluation must be hig...
Generic drugs are copies of brand-name drugs that have exactly the same dosage, intended use, effect...
R educing health costs is a hot political issue in manycountries, so the introduction and use of gen...
BACKGROUND AND OBJECTIVES: Generic substitution has become a common practice since the late 1970s in...
This review article discusses the similarities and differences in the research, production and use i...
peer reviewedComplementarily to a previous publication, this paper tries to answer a few commonly as...
Generic drugs are medicines which are identical, or are bioequivalent to brand name drugs in dosage,...
In the last one decade, due to expiry of patented products as well as their exclusivity period, a dr...
The concept of: Generic drugs and patented drugs vs. brand name drugs and non-proprietary (generic) ...
Patents for several blockbuster biological products are expected to expire soon. The Food and Drug A...
The Author(s) 2015. This article is published with open access at Springerlink.com A generic medicin...