Between 1919 and the late 1960s, prominent manufacturers of proprietary articles represented by the Proprietary Association of Great Britain (PAGB) developed a code of advertising standards in relation to proprietary medicines and allied articles. The commitment to minimum standards of conduct was intended by associated manufacturers to generate a level of trust and credibility in their industry capable of protecting it from the possibility of unprecedented government intervention. Such an intervention was premised on a perception amongst some government ministers, medical professionals and social justice advocates that ‘patent’, ‘secret’ and ‘proprietary’ medicines constituted a network of fraud and deliberate crime against the wellbeing o...
Britain in the final decades of the nineteenth century was a vibrant market place for purveyors of m...
Summary. Trust is not automatically granted to providers of professional services. The doctors of Ge...
Drawing on case studies from the modern era of pharmaceutical regulation in the UK, US and Europe, I...
In 1909, the British Medical Association published an exposé of the patent medicine trade, Secret Re...
industry self-regulatory bodies are tasked with supervising compliance with marketing rules. The obj...
Within last twenty years in the European Union much regulation concerning advertisements of drugs ch...
In many European countries, medicines promotion is governed by voluntary codes of practice administe...
pharmaceutical promotion: What happens when companies breach advertising guidelines? Joel Lexchin, M...
Popular narrative has equated branded medicines with quacks selling patent medicines to a gullible p...
It is held that under perfect market mechanisms, there would be need neither for product safety regu...
Federal trade commission regulation of pharmaceutical advertising is a subject of considerable curre...
The adverse consequences of the use of thalidomide in the 1950s and 1960s by pregnant women, instiga...
Medicine advertisements need to be controlled to ensure public interest is protected from harm and c...
Abstract, Jan Metelka The main aim of this diploma thesis was to firstly explain the field of human ...
"For the first time in August 1894, phials of anti-diphtheria serum went on sale in German pharmacie...
Britain in the final decades of the nineteenth century was a vibrant market place for purveyors of m...
Summary. Trust is not automatically granted to providers of professional services. The doctors of Ge...
Drawing on case studies from the modern era of pharmaceutical regulation in the UK, US and Europe, I...
In 1909, the British Medical Association published an exposé of the patent medicine trade, Secret Re...
industry self-regulatory bodies are tasked with supervising compliance with marketing rules. The obj...
Within last twenty years in the European Union much regulation concerning advertisements of drugs ch...
In many European countries, medicines promotion is governed by voluntary codes of practice administe...
pharmaceutical promotion: What happens when companies breach advertising guidelines? Joel Lexchin, M...
Popular narrative has equated branded medicines with quacks selling patent medicines to a gullible p...
It is held that under perfect market mechanisms, there would be need neither for product safety regu...
Federal trade commission regulation of pharmaceutical advertising is a subject of considerable curre...
The adverse consequences of the use of thalidomide in the 1950s and 1960s by pregnant women, instiga...
Medicine advertisements need to be controlled to ensure public interest is protected from harm and c...
Abstract, Jan Metelka The main aim of this diploma thesis was to firstly explain the field of human ...
"For the first time in August 1894, phials of anti-diphtheria serum went on sale in German pharmacie...
Britain in the final decades of the nineteenth century was a vibrant market place for purveyors of m...
Summary. Trust is not automatically granted to providers of professional services. The doctors of Ge...
Drawing on case studies from the modern era of pharmaceutical regulation in the UK, US and Europe, I...