Biotechnology Law - Regulators of Biotechnology Products, Food and Drug Administration, United States Environmental Protection Agency (Paperback)


Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 49. Chapters: Regulators of biotechnology products, Food and Drug Administration, United States Environmental Protection Agency, Stem cell laws and policy in the United States, Monsanto Canada Inc. v. Schmeiser, Portable Emissions Measurement System, Bayh-Dole Act, Orphan drug, Drug Price Competition and Patent Term Restoration Act, European Medicines Agency, Environment Canada, Animal and Plant Health Inspection Service, Plant Variety Protection Act of 1970, Diamond v. Chakrabarty, Biodefense and Pandemic Vaccine and Drug Development Act of 2005, Center for Biologics Evaluation and Research, Research exemption, Health Canada, Ministry of Health, Labour and Welfare, MedImmune, Inc. v. Genentech, Inc., Stem cell laws and policy in China, National Institute for Biological Standards and Control, Merck KGaA v. Integra Lifesciences I, Ltd., Ariad v. Lilly, Medicines and Healthcare products Regulatory Agency, Agriculture and Agri-Food Canada, Cabilly patents, LabCorp v. Metabolite, Inc, Roche Products v. Bolar Pharmaceutical, Eli Lilly & Co. v. Medtronic, Inc., Plant Patent Act of 1930, Biologics Control Act, New Zealand Food Safety Authority, Patients Not Patents, Natural Health Products Directorate, National Health Surveillance Agency, Health Products and Food Branch, Federal Agency for Medicines and Health Products, Norwegian Medicines Agency, Oncology Drug Advisory Committee. Excerpt: The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusio...

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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 49. Chapters: Regulators of biotechnology products, Food and Drug Administration, United States Environmental Protection Agency, Stem cell laws and policy in the United States, Monsanto Canada Inc. v. Schmeiser, Portable Emissions Measurement System, Bayh-Dole Act, Orphan drug, Drug Price Competition and Patent Term Restoration Act, European Medicines Agency, Environment Canada, Animal and Plant Health Inspection Service, Plant Variety Protection Act of 1970, Diamond v. Chakrabarty, Biodefense and Pandemic Vaccine and Drug Development Act of 2005, Center for Biologics Evaluation and Research, Research exemption, Health Canada, Ministry of Health, Labour and Welfare, MedImmune, Inc. v. Genentech, Inc., Stem cell laws and policy in China, National Institute for Biological Standards and Control, Merck KGaA v. Integra Lifesciences I, Ltd., Ariad v. Lilly, Medicines and Healthcare products Regulatory Agency, Agriculture and Agri-Food Canada, Cabilly patents, LabCorp v. Metabolite, Inc, Roche Products v. Bolar Pharmaceutical, Eli Lilly & Co. v. Medtronic, Inc., Plant Patent Act of 1930, Biologics Control Act, New Zealand Food Safety Authority, Patients Not Patents, Natural Health Products Directorate, National Health Surveillance Agency, Health Products and Food Branch, Federal Agency for Medicines and Health Products, Norwegian Medicines Agency, Oncology Drug Advisory Committee. Excerpt: The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusio...

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Product Details

General

Imprint

Books LLC, Wiki Series

Country of origin

United States

Release date

July 2011

Availability

Supplier out of stock. If you add this item to your wish list we will let you know when it becomes available.

First published

July 2011

Authors

Creators

Dimensions

246 x 189 x 3mm (L x W x T)

Format

Paperback - Trade

Pages

50

ISBN-13

978-1-157-46809-7

Barcode

9781157468097

Categories

LSN

1-157-46809-8



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