The rate of new drug approvals in the US has remained essentially constant since 1950, while the costs of drug development have soared. Many commentators question the sustainability of the current model of drug development, in which large pharmaceutical companies incur markedly escalating costs to deliver the same number of products to market. This Issue Brief summarizes the problem, describes ongoing governmental efforts to influence the process, and suggests changes in regulatory science and translational medicine that may promote more successful development of safe and effective therapeutics
Thesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology, 2004.Includes bibliographical...
Recently the Federal Circuit has adopted a sweeping new rule of inherent anticipation that essential...
AbstractRecent growth in annual new therapeutic entity (NTE) approvals by the U.S. Food and Drug Adm...
The rate of new drug approvals in the US has remained essentially constant since 1950, while the cos...
The research, development, and approval of a drug product is a continuous but lengthy process involv...
The average cost to develop each new pharmaceutical drug is approximately $1 billion or more and tak...
For latest version: please go to https://academicentrepreneurship.pubpub.org/pub/8a05fz36/release/4 ...
The efficiency of pharmaceutical research and development (R&D) reflected by increasing costs of R&D...
"Containing contributions from the many disciplines involved in a drug's evolution, this timely volu...
An explosion of knowledge and a growing array of tools and technologies have transformed modern drug...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Comp...
Developing new drugs for cancer and or any other medical purpose is a tedious, complex, expensive pr...
Drug development has become the exclusive activity of large pharmaceutical companies. However, the o...
Despite the large number of new medicines entering the market every year, the vast majority offer fe...
On August 15, 2005, the Food and Drug Administration (FDA) and the Association of American Medical C...
Thesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology, 2004.Includes bibliographical...
Recently the Federal Circuit has adopted a sweeping new rule of inherent anticipation that essential...
AbstractRecent growth in annual new therapeutic entity (NTE) approvals by the U.S. Food and Drug Adm...
The rate of new drug approvals in the US has remained essentially constant since 1950, while the cos...
The research, development, and approval of a drug product is a continuous but lengthy process involv...
The average cost to develop each new pharmaceutical drug is approximately $1 billion or more and tak...
For latest version: please go to https://academicentrepreneurship.pubpub.org/pub/8a05fz36/release/4 ...
The efficiency of pharmaceutical research and development (R&D) reflected by increasing costs of R&D...
"Containing contributions from the many disciplines involved in a drug's evolution, this timely volu...
An explosion of knowledge and a growing array of tools and technologies have transformed modern drug...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Comp...
Developing new drugs for cancer and or any other medical purpose is a tedious, complex, expensive pr...
Drug development has become the exclusive activity of large pharmaceutical companies. However, the o...
Despite the large number of new medicines entering the market every year, the vast majority offer fe...
On August 15, 2005, the Food and Drug Administration (FDA) and the Association of American Medical C...
Thesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology, 2004.Includes bibliographical...
Recently the Federal Circuit has adopted a sweeping new rule of inherent anticipation that essential...
AbstractRecent growth in annual new therapeutic entity (NTE) approvals by the U.S. Food and Drug Adm...