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FDA Regulatory Affairs
Third Edition
Taschenbuch von David Mantus (u. a.)
Sprache: Englisch

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Beschreibung

Including contributions from leading experts at organizations such as the FDA, NIH, and PAREXEL, the Third Edition of this highly successful, jargon-free publication serves as a roadmap to prescription drug, biologics, and medical device development in the US.

Including contributions from leading experts at organizations such as the FDA, NIH, and PAREXEL, the Third Edition of this highly successful, jargon-free publication serves as a roadmap to prescription drug, biologics, and medical device development in the US.

Über den Autor

David Mantus worked in the biotechnology and pharmaceutical industry for more than 20 years. He not only served as vice president of regulatory affairs at Cubist Pharmaceuticals but also held various regulatory roles at Sention Inc., Shire Biologics, PAREXEL, the Massachusetts Public Health Laboratory, the Massachusetts College of Pharmacy and Health Sciences, and Procter and Gamble Pharmaceuticals. He received his BS in chemistry from the College of William and Mary, his MS and Ph.D in chemistry from Cornell University, and was a post-doctoral research fellow in biomedical engineering at the University of Washington. He is currently associate professor of pharmaceutical sciences and director, regulatory affairs at MCPHS University in Boston.

Douglas J. Pisano received his Ph.D in law, policy, and society from Northeastern University. He has participated on the editorial advisory boards of multiple journals and received the Special Service Award for the Enhancement of Regulatory Education from the Regulatory Affairs Professionals Society. A registered pharmacist and active member of several professional organizations, including the American Association of Colleges of Pharmacy and the Regulatory Affairs Professionals Society, he formerly served as dean of the School of Pharmacy-Boston and is currently professor of pharmacy administration, vice-president of academic affairs, and provost at MCPHS University in Boston.

Inhaltsverzeichnis

Overview of FDA and Drug Development. What Is an IND? The New Drug Application. Meetings with the FDA. FDA Medical Device Regulation. A Primer of Drug/Device Law: What Is the Law and How Do I Find It? The Development of Orphan Drugs. CMC Sections of Regulatory Filings and CMC Regulatory Compliance during Investigational and Postapproval Stages. Overview of the GxPs for the Regulatory Professional. FDA Regulation of the Advertising and Promotion of Prescription Drugs, Biologics, and Medical Devices. The Practice of Regulatory Affairs. FDA Advisory Committees. Biologics. Regulation of Combination Products in the United States.

Details
Erscheinungsjahr: 2024
Fachbereich: Handels- und Wirtschaftsrecht, Arbeitsrecht
Genre: Importe, Recht
Produktart: Nachschlagewerke
Rubrik: Recht & Wirtschaft
Medium: Taschenbuch
Inhalt: Einband - flex.(Paperback)
ISBN-13: 9781032920542
ISBN-10: 1032920548
Sprache: Englisch
Einband: Kartoniert / Broschiert
Redaktion: Mantus, David
Pisano, Douglas J.
Auflage: 3. Auflage
Hersteller: Taylor & Francis Ltd
Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, D-36244 Bad Hersfeld, gpsr@libri.de
Maße: 152 x 229 x 24 mm
Von/Mit: David Mantus (u. a.)
Erscheinungsdatum: 14.10.2024
Gewicht: 0,566 kg
Artikel-ID: 129951120
Über den Autor

David Mantus worked in the biotechnology and pharmaceutical industry for more than 20 years. He not only served as vice president of regulatory affairs at Cubist Pharmaceuticals but also held various regulatory roles at Sention Inc., Shire Biologics, PAREXEL, the Massachusetts Public Health Laboratory, the Massachusetts College of Pharmacy and Health Sciences, and Procter and Gamble Pharmaceuticals. He received his BS in chemistry from the College of William and Mary, his MS and Ph.D in chemistry from Cornell University, and was a post-doctoral research fellow in biomedical engineering at the University of Washington. He is currently associate professor of pharmaceutical sciences and director, regulatory affairs at MCPHS University in Boston.

Douglas J. Pisano received his Ph.D in law, policy, and society from Northeastern University. He has participated on the editorial advisory boards of multiple journals and received the Special Service Award for the Enhancement of Regulatory Education from the Regulatory Affairs Professionals Society. A registered pharmacist and active member of several professional organizations, including the American Association of Colleges of Pharmacy and the Regulatory Affairs Professionals Society, he formerly served as dean of the School of Pharmacy-Boston and is currently professor of pharmacy administration, vice-president of academic affairs, and provost at MCPHS University in Boston.

Inhaltsverzeichnis

Overview of FDA and Drug Development. What Is an IND? The New Drug Application. Meetings with the FDA. FDA Medical Device Regulation. A Primer of Drug/Device Law: What Is the Law and How Do I Find It? The Development of Orphan Drugs. CMC Sections of Regulatory Filings and CMC Regulatory Compliance during Investigational and Postapproval Stages. Overview of the GxPs for the Regulatory Professional. FDA Regulation of the Advertising and Promotion of Prescription Drugs, Biologics, and Medical Devices. The Practice of Regulatory Affairs. FDA Advisory Committees. Biologics. Regulation of Combination Products in the United States.

Details
Erscheinungsjahr: 2024
Fachbereich: Handels- und Wirtschaftsrecht, Arbeitsrecht
Genre: Importe, Recht
Produktart: Nachschlagewerke
Rubrik: Recht & Wirtschaft
Medium: Taschenbuch
Inhalt: Einband - flex.(Paperback)
ISBN-13: 9781032920542
ISBN-10: 1032920548
Sprache: Englisch
Einband: Kartoniert / Broschiert
Redaktion: Mantus, David
Pisano, Douglas J.
Auflage: 3. Auflage
Hersteller: Taylor & Francis Ltd
Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, D-36244 Bad Hersfeld, gpsr@libri.de
Maße: 152 x 229 x 24 mm
Von/Mit: David Mantus (u. a.)
Erscheinungsdatum: 14.10.2024
Gewicht: 0,566 kg
Artikel-ID: 129951120
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