Author: Publisher:
ISBN:
Category : Antibiotics
Languages : en
Pages : 46
Book Description
Guideline on Formatting, Assembling, and Submitting New Drug and Antibiotic Applications
Author: Guideline on Formatting, Assembling, and Submitting New Drug and Antibiotic Applications
Author: DIANE Publishing CompanyPublisher: DIANE Publishing
ISBN: 0788147846
Category :
Languages : en
Pages : 65
Book Description
Guideline on Formatting, Assembling, and Submitting New Drug and Antibiotic Applications
Author: BPI Information ServicesPublisher: Bpi Information Services
ISBN: 9781579791605
Category :
Languages : en
Pages : 40
Book Description
The Federal Food, Drug, and Cosmetic Act provides that a new drug may not be introduced or delivered for introduction into interstate commerce unless the Food and Drug Administration (FDA) has approved a new drug application for it, and only if the applicant demonstrates by adequate scientific evidence that the drug is safe and by substantial evidence that the drug is effective for the conditions prescribed, recommended, or suggested in proposed labeling for the product.
Federal Register
Author: Drug Development
Author: Charles E. HamnerPublisher: CRC Press
ISBN: 0429552998
Category : Medical
Languages : en
Pages : 319
Book Description
Published in 1990: Overall the volume stands as a relatively comprehensive but not exhaustive summation of the complex process of drug development.
Pharmaceutical Dosage Forms
Author: Kenneth E. AvisPublisher: Routledge
ISBN: 1351425188
Category : Medical
Languages : en
Pages : 592
Book Description
Completely updated and enlarged to three volumes (originally published as two volumes), the Second Edition of Pharmaceutical Dosage Forms: Parenteral Medications examines every important aspect of sterile drug products. This volume (3) offers comprehensive coverage of medical devices, quality assurance and regulatory issues.;This in-depth reference and text: discusses regulatory requirements in record-keeping based on the US Food and Drug Administration's (FDA) Current Good Manufacturing Practices; places special emphasis on methods of detecting, counting and sizing particles; offers new perspectives on contemporary validation concepts and how they affect the validation process; explains current FDA enforcement activities, the voluntary compliance policy, select court cases, and how these relate to parenterals; provides recent materials on the use of audits as a means of verifying the efficacy of manufacturing control systems; highlights new US regulations for medical devices; and examines quality assurance, including new information on biological control tests for medical device materials.;With the contributions of leading experts, volume 3 of Pharmaceutical Dosage Forms: Parenteral Medications is intended as a day-to-day reference for pharmacists, medical device manufacturers, quality control and regulatory personnel, chemists and drug patent and litigation attorneys, as well as a text for upper-level undergraduate, graduate and continuing-education students in the pharmaceutical sciences.
FDA Medical Library Serials Holdings List
Author: United States. Food and Drug Administration. Medical LibraryPublisher:
ISBN:
Category : Medical literature
Languages : en
Pages : 136
Book Description
Practical Pharmaceutical Engineering
Author: Gary PragerPublisher: John Wiley & Sons
ISBN: 1119418844
Category : Science
Languages : en
Pages : 575
Book Description
A practical guide to all key the elements of pharmaceuticals and biotech manufacturing and design Engineers working in the pharmaceutical and biotech industries are routinely called upon to handle operational issues outside of their fields of expertise. Traditionally the competencies required to fulfill those tasks were achieved piecemeal, through years of self-teaching and on-the-job experience—until now. Practical Pharmaceutical Engineering provides readers with the technical information and tools needed to deal with most common engineering issues that can arise in the course of day-to-day operations of pharmaceutical/biotech research and manufacturing. Engineers working in pharma/biotech wear many hats. They are involved in the conception, design, construction, and operation of research facilities and manufacturing plants, as well as the scale-up, manufacturing, packaging, and labeling processes. They have to implement FDA regulations, validation assurance, quality control, and Good Manufacturing Practices (GMP) compliance measures, and to maintain a high level of personal and environmental safety. This book provides readers from a range of engineering specialties with a detailed blueprint and the technical knowledge needed to tackle those critical responsibilities with confidence. At minimum, after reading this book, readers will have the knowledge needed to constructively participate in contractor/user briefings. Provides pharmaceutical industry professionals with an overview of how all the parts fit together and a level of expertise that can take years of on-the-job experience to acquire Addresses topics not covered in university courses but which are crucial to working effectively in the pharma/biotech industry Fills a gap in the literature, providing important information on pharmaceutical operation issues required for meeting regulatory guidelines, plant support design, and project engineering Covers the basics of HVAC systems, water systems, electric systems, reliability, maintainability, and quality assurance, relevant to pharmaceutical engineering Practical Pharmaceutical Engineering is an indispensable “tool of the trade” for chemical engineers, mechanical engineers, and pharmaceutical engineers employed by pharmaceutical and biotech companies, engineering firms, and consulting firms. It also is a must-read for engineering students, pharmacy students, chemistry students, and others considering a career in pharmaceuticals.
FDA Medical Library Serials Holdings List
Author: Sylvia A. BullockPublisher:
ISBN:
Category : Government publications
Languages : en
Pages : 136
Book Description
Author: