Fundamentals of US Regulatory Affairs

Fundamentals of US Regulatory Affairs PDF Author:
Publisher:
ISBN:
Category : Biologicals
Languages : en
Pages : 540

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Book Description

Fundamentals of US Regulatory Affairs

Fundamentals of US Regulatory Affairs PDF Author:
Publisher:
ISBN:
Category : Biologicals
Languages : en
Pages : 540

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Book Description


Fundamentals of US Regulatory Affairs, Sixth Edition

Fundamentals of US Regulatory Affairs, Sixth Edition PDF Author: Peggy Berry
Publisher:
ISBN: 9780978700621
Category : Pharmaceutical policy
Languages : en
Pages : 464

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Book Description


Fundamentals of US Regulatory Affairs, Eighth Edition

Fundamentals of US Regulatory Affairs, Eighth Edition PDF Author: Alix E. Alderman
Publisher:
ISBN: 9780982932063
Category : Biologicals
Languages : en
Pages : 552

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Book Description


Fundamentals of Us Regulatory Affairs 2005

Fundamentals of Us Regulatory Affairs 2005 PDF Author: Mika Reinikainen
Publisher:
ISBN: 9780967311579
Category : Business & Economics
Languages : en
Pages : 265

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Book Description
Directives and regulations governing healthcare products in the EU.

Fundamentals of International Regulatory Affairs, Fifth Edition

Fundamentals of International Regulatory Affairs, Fifth Edition PDF Author: Gloria Hall
Publisher:
ISBN: 9781947493636
Category :
Languages : en
Pages :

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Book Description


Regulatory Affairs in the Pharmaceutical Industry

Regulatory Affairs in the Pharmaceutical Industry PDF Author: Javed Ali
Publisher: Academic Press
ISBN: 0128222239
Category : Medical
Languages : en
Pages : 287

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Book Description
Regulatory Affairs in the Pharmaceutical Industry is a comprehensive reference that compiles all the information available pertaining to regulatory procedures currently followed by the pharmaceutical industry. Designed to impart advanced knowledge and skills required to learn the various concepts of regulatory affairs, the content covers new drugs, generic drugs and their development, regulatory filings in different countries, different phases of clinical trials, and the submission of regulatory documents like IND (Investigational New Drug), NDA (New Drug Application) and ANDA (Abbreviated New Drug Application). Chapters cover documentation in the pharmaceutical industry, generic drug development, code of Federal Regulation (CFR), the ANDA regulatory approval process, the process and documentation for US registration of foreign drugs, the regulation of combination products and medical devices, the CTD and ECTD formats, and much more. Updated reference on drug approval processes in key global markets Provides comprehensive coverage of concepts and regulatory affairs Presents a concise compilation of the regulatory requirements of different countries Introduces the fundamentals of manufacturing controls and their regulatory importance

Fundamentals of Regulatory Affairs

Fundamentals of Regulatory Affairs PDF Author: Regulatory Affairs Professionals Society
Publisher:
ISBN:
Category : Biologicals
Languages : en
Pages : 270

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Book Description


Fundamentals of International Regulatory Affairs

Fundamentals of International Regulatory Affairs PDF Author: Pamela Anne Jones
Publisher:
ISBN: 9781947493179
Category :
Languages : en
Pages : 502

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Book Description


2000 Supplement

2000 Supplement PDF Author: Regulatory Affairs Professionals Society
Publisher:
ISBN:
Category : Biologicals
Languages : en
Pages : 93

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Book Description


Us Regulatory Affairs Questionnaire

Us Regulatory Affairs Questionnaire PDF Author: Ashwani Khurana
Publisher:
ISBN: 9780615789187
Category :
Languages : en
Pages :

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Book Description
This book presents multiple choice questions for testing knowledge in US regulatory affairs covering areas of drug, device and biologics.