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2005, 2, Drugs and the pharmaceutical sciences, ISBN 9780824754648, Volume 144, 650
.... It focuses on major legislative revisions that impact requirements for drug safety reviews, product regulatory approvals, and marketing practices... 
Drugs | Law and legislation | Pharmacy | Pharmaceutical Manufacturing | Pharmaceutical Science Regulatory | Analysis & Pharmaceutical Quality | United States
eBook
2010, Princeton studies in American politics, ISBN 0691141800, xx, 802
The U.S. Food and Drug Administration is the most powerful regulatory agency in the world. How did the FDA become so influential? And how exactly does it wield... 
Pharmaceutical policy | Drugs | United States. Food and Drug Administration | United States | Research | History | Political Science | Health Sciences | Public Policy | POLITICAL SCIENCE | HISTORY | Food and Drug Administration
Book
SAE technical paper series, Volume 2006-01-0116.
Automotive engineering is continously moving toward the integration of different processes for accelerating vehicle development. Since the products become more... 
Computer simulation | Materials | Quality control | Durability | Mathematical models | Product development
eJournal
2009, 5th ed., Drugs and the pharmaceutical sciences, ISBN 9781420088496, Volume 190., xviii, 529
The thoroughly revised Fifth Edition of New Drug Approval Process supplies readers with the latest global changes that affect pharmaceutical product approval and influence how new products are researched... 
Drugs | Drug Evaluation | Clinical Trials as Topic | New products | Drug approval | Government policy | Standards | Testing | Clinical Trials - Pharmaceutical Science | Pharmaceutical Science Regulatory | Drug Design & Development | United States
Book
2012, 1., Etudes Linguistiques = Linguistische Studien, ISBN 9783936609578, Volume 9
Book
SAE technical paper series, Volume 885159.
In 1970 the EEC adopted a framework directive (70/156/EEC) on a European type approval... 
Globalization | Environmental regulations and standards
eJournal
SAE technical paper series, Volume 982839.
.... Therefore, the durability approval must be carried out under representative service-like loading, which take into account complex leaf deformations in operational usage... 
Suspension systems | Steering systems | Maintainability and supportability | Springs
eJournal
SAE technical paper series, Volume 2007-01-2724.
The approval of bearings for mechanical transmissions is generally done through an accelerated bench test, which is based on calculated bearing life... 
Transmissions | Bearings | Manual transmissions | Mathematical models | Safety
eJournal
SAE technical paper series, Volume 982840.
... and the procedure for an optimum light-weight design is treated. Finally, the test procedure for durability approval, the corresponding test facility, the test programs... 
Steering systems | Bearings | Braking systems
eJournal
SAE technical paper series, Volume 2007-01-2959.
Transportation has been understood today as an essential activity in the life of people all around the world. The efficiency of the transport systems is an... 
Manufacturing processes | Maintenance and Aftermarket | Mathematical models | Product development | Materials identification | Steel | Plastics
eJournal
SAE technical paper series, Volume 2001-01-3866.
Quality planning reduces cost, increases productivity, rationalizes investments and improves competitiveness. This is of great importance when referring to the... 
Productivity | Diesel / Compression Ignition engines | Production control | Quality control | Product development
eJournal
SAE technical paper series, Volume 760145.
The Automobile Club of Southern California has a responsibility of responding to the needs of the motoring public. With the complexity and sophistication of... 
Maintenance, repair, and service operations
eJournal
2012, Potsdam cognitive science series, ISBN 3869561785, Volume 3, i, 66
Book
Journal Article
The Journal of Bone and Joint Surgery, ISSN 0021-9355, 03/2017, Volume 99, Issue 6, pp. e26 - e26
The 2 main routes of medical device approval through the U.S. Food and Drug Administration are the premarket approval (PMA... 
SURGERY | MEDICAL DEVICES | ORTHOPEDICS | RECALLS | Policy | United States | Humans | Orthopedics | Product Surveillance, Postmarketing | Equipment Safety | Device Approval | United States Food and Drug Administration | Orthopedic Equipment
Journal Article
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