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International Journal of Drug Regulatory Affairs; 2014, 2(1), 1- 11 Abstract: Developing a new drug requires great amount of research work in chemistry, manufacturing, controls, preclinical science and clinical trials. Drug reviewers in regulatory agencies around the world bear the responsibility of evaluating whether the research data support the safety, effectiveness and quality control of a new drug product to serve the public health. Every country has its own regulatory authority, which is responsible to enforce the rules and regulations and issue the guidelines to regulate the marketing of the drugs. This article focuses on drug approval process in different countries like USA, Europe and India.]]>

International Journal of Drug Regulatory Affairs; 2014, 2(1), 1- 11 Abstract: Developing a new drug requires great amount of research work in chemistry, manufacturing, controls, preclinical science and clinical trials. Drug reviewers in regulatory agencies around the world bear the responsibility of evaluating whether the research data support the safety, effectiveness and quality control of a new drug product to serve the public health. Every country has its own regulatory authority, which is responsible to enforce the rules and regulations and issue the guidelines to regulate the marketing of the drugs. This article focuses on drug approval process in different countries like USA, Europe and India.]]>
Tue, 27 May 2014 05:12:00 GMT /slideshow/ijdra-119/35160182 JEETBADJATYA123@slideshare.net(JEETBADJATYA123) A REVIEW ON DRUG APPROVAL PROCESS FOR US, EUROPE AND INDIA JEETBADJATYA123 International Journal of Drug Regulatory Affairs; 2014, 2(1), 1- 11 Abstract: Developing a new drug requires great amount of research work in chemistry, manufacturing, controls, preclinical science and clinical trials. Drug reviewers in regulatory agencies around the world bear the responsibility of evaluating whether the research data support the safety, effectiveness and quality control of a new drug product to serve the public health. Every country has its own regulatory authority, which is responsible to enforce the rules and regulations and issue the guidelines to regulate the marketing of the drugs. This article focuses on drug approval process in different countries like USA, Europe and India. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/ijdra119-140527051200-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> International Journal of Drug Regulatory Affairs; 2014, 2(1), 1- 11 Abstract: Developing a new drug requires great amount of research work in chemistry, manufacturing, controls, preclinical science and clinical trials. Drug reviewers in regulatory agencies around the world bear the responsibility of evaluating whether the research data support the safety, effectiveness and quality control of a new drug product to serve the public health. Every country has its own regulatory authority, which is responsible to enforce the rules and regulations and issue the guidelines to regulate the marketing of the drugs. This article focuses on drug approval process in different countries like USA, Europe and India.
A REVIEW ON DRUG APPROVAL PROCESS FOR US, EUROPE AND INDIA from International Journal of Drug Regulatory Affairs
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https://cdn.slidesharecdn.com/profile-photo-JEETBADJATYA123-48x48.jpg?cb=1523499051 International Journal of Drug Regulatory Affairs: IJDRA a broad-spectrum, open-access & peer-reviewed International Pharmaceutical Journal circulated electronically via the world wide web. It cover the subjects - Regulatory Affairs, Intellectual Property Rights and Pharmaceutical Development and intended to be of interest to a broad audience of pharmaceutical professionals. IJDRA now ideally placed to serve the needs of their readers and advertisers related to pharmaceutical field. www.ijdra.com/