Lassman examines the tension between transparency and other public health interests in the context of the FDA\u27s proposed Drug Watch web site. He argues that although the FDA proposal seeks to achieve a laudable goal--the prompt communication of important useful safety information about drug products to physicians and patients-- it fails to properly balance transparency and other legitimate public health interests
Transparency has risen to prominence in risk regulation leading government authorities in Europe and...
Efforts to foster transparency in biopharmaceutical regulation are well underway: drug manufacturers...
Transparency is now recognized to play a crucial role in increasing accountability in health care [1...
In the arena of pharmaceutical drug regulation, transparency is the favoured focus of many current p...
In Europe and North America, there is increasing political pressure being put on health regulatory a...
The Internet is becoming the greatest source of health information for most consumers, which reinfor...
Biopharmaceutical companies submit vast amounts of clinical data and analysis to support approval of...
Scandals of selective reporting of clinical trial results by pharmaceutical firms have underlined th...
Scandals of selective reporting of clinical trial results by pharmaceutical \u85rms have under-lined...
Recent allegations that essential safety and efficacy information is often suppressed by medical pro...
To obtain approval to market a drug, a manufacturer must disclose significant amounts of research da...
Although [drug] manufacturers bear the cost of research data generation, it is oftentimes a worthwhi...
Those committed to the free exchange of scientific information have long complained about various re...
Over the past 10 years, European pharmaceutical regulators (especially the European Medicines Agency...
Over the past 10years, European pharmaceutical regulators (especially the European Medicines Agency ...
Transparency has risen to prominence in risk regulation leading government authorities in Europe and...
Efforts to foster transparency in biopharmaceutical regulation are well underway: drug manufacturers...
Transparency is now recognized to play a crucial role in increasing accountability in health care [1...
In the arena of pharmaceutical drug regulation, transparency is the favoured focus of many current p...
In Europe and North America, there is increasing political pressure being put on health regulatory a...
The Internet is becoming the greatest source of health information for most consumers, which reinfor...
Biopharmaceutical companies submit vast amounts of clinical data and analysis to support approval of...
Scandals of selective reporting of clinical trial results by pharmaceutical firms have underlined th...
Scandals of selective reporting of clinical trial results by pharmaceutical \u85rms have under-lined...
Recent allegations that essential safety and efficacy information is often suppressed by medical pro...
To obtain approval to market a drug, a manufacturer must disclose significant amounts of research da...
Although [drug] manufacturers bear the cost of research data generation, it is oftentimes a worthwhi...
Those committed to the free exchange of scientific information have long complained about various re...
Over the past 10 years, European pharmaceutical regulators (especially the European Medicines Agency...
Over the past 10years, European pharmaceutical regulators (especially the European Medicines Agency ...
Transparency has risen to prominence in risk regulation leading government authorities in Europe and...
Efforts to foster transparency in biopharmaceutical regulation are well underway: drug manufacturers...
Transparency is now recognized to play a crucial role in increasing accountability in health care [1...