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Pharmaceutical vendors approval manual, Asif, Erfan Syed


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Цена: 86760.00T
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Склад Америка: 198 шт.  
При оформлении заказа до: 2025-08-18
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Автор: Asif, Erfan Syed
Название:  Pharmaceutical vendors approval manual
ISBN: 9781032030883
Издательство: Taylor&Francis
Классификация:



ISBN-10: 1032030887
Обложка/Формат: Hardcover
Страницы: 152
Вес: 0.40 кг.
Дата издания: 13.12.2021
Язык: English
Иллюстрации: 1 line drawings, black and white; 1 halftones, black and white; 2 illustrations, black and white
Размер: 23.39 x 15.60 x 1.12 cm
Подзаголовок: A comprehensive quality manual for api and packaging material approval
Рейтинг:
Поставляется из: Европейский союз
Описание: This book provides stepwise guidance on how to evaluate, audit, qualify and approve an active pharmaceutical ingredient (API) and packaging material manufacturer and supplier to enhance the GMP within the industry. The book will also be beneficial for institutions conducting pharmaceutical technology courses in terms of GMP and GLP applications. The Pharmaceutical Vendors Approval Manual provides readers and front-line health care products manufacturers, R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements. This book provides a simple, concise and easy to use reference tool covering basic quality concepts and the elements of vendor’s assessment, qualification and approval required by the pharmaceutical educational institutions and professional certification bodies. It is equally relevant to Quality Assurance officers, Quality Control Analysts, Quality Auditors and other personnel involved in GMP/GLP services in the company. The book will also be beneficial for the institutions conducting Pharmaceutical technology study courses in terms of GMP and GLP applications.This bookprovides readers and front-line health care products manufacturers, R&D management and biotech laboratories all the information they need to know to develop a GMP-oriented industry with trained and skilled personnel and manufacture products that meet GMP and regulatory requirements covers basic quality concepts and the elements of vendor’s assessment, qualification and approval required by the pharmaceutical educational institutions and professional certification bodies provides stepwise guidance on how to evaluate, audit, qualify and approve an API and packaging material manufacturer and supplier to enhance the GMP within the industry
Дополнительное описание: 1. Finding and Partnering Active Pharmaceutical Ingredients Vendor.  2. Selection of API Vendors and the impacts on Drug products.  3. Approach, Team formation and Planning.  4. Site Standard Operating Procedure for vendors approv


Drugs: From Discovery to Approval

Автор: Rick Ng
Название: Drugs: From Discovery to Approval
ISBN: 1118907272 ISBN-13(EAN): 9781118907276
Издательство: Wiley
Рейтинг:
Цена: 88650.00 T
Наличие на складе: Есть у поставщика Поставка под заказ.
Описание: The third edition of this best–selling book continues to offer a user–friendly, step–by–step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre–clinical studies, the conduct of human clinical trials, regulatory controls, and even the manufacturing processes for pharmaceutical products. Concise and easy to read, Drugs: From Discovery to Approval, Third Edition quickly introduces basic concepts and then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs. The third edition incorporates the latest developments and updates in the pharmaceutical community, provides more comprehensive coverage of topics, and includes more materials and case studies suited to college and university use. Biotechnology is a dynamic field with changes across R&D, clinical trials, manufacturing, and regulatory processes; the third edition of the text provides timely updates for those in this rapidly growing field. • Revised edition will have greater appeal to students with the inclusion of more materials and case studies suited to college and university use • Includes the latest developments and updates • Increased appeal by provision of more comprehensive topics

Preparing for FDA Pre-Approval Inspections

Название: Preparing for FDA Pre-Approval Inspections
ISBN: 0367452715 ISBN-13(EAN): 9780367452711
Издательство: Taylor&Francis
Рейтинг:
Цена: 63280.00 T
Наличие на складе: Есть у поставщика Поставка под заказ.
Описание:

This Second Edition is an essential guide to preparing for FDA pre-approval inspections--taking into account current trends in FDA expectations and inspection activities, such as the GMPs of the 21st Century, quality systems-based approach to inspections, risk-based inspections, quality by design, process analytical technology, design space, etc. The goal of this book is to help organizations gain rapid regulatory approval.





Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition:







  • chronicles the major shifts in inspection activity as evidenced by a systems-based approach to inspections


  • demonstrates what each area of pharmaceutical development, from research and development to training, is expected to provide to inspectors


  • focuses on traditional development and submission activities, but also discusses cases where the transfer is from a domestic site to an international facility

Cleaning validation manual

Автор: Haider, Syed Imtiaz (gulf Pharmaceutical Industries, United Arab Emirates)
Название: Cleaning validation manual
ISBN: 1138749710 ISBN-13(EAN): 9781138749719
Издательство: Taylor&Francis
Рейтинг:
Цена: 117390.00 T
Наличие на складе: Есть у поставщика Поставка под заказ.
Описание: With over 20 easy-to-use template protocols for cleaning validation of extensively used equipments, this book provides technical solutions to assist in fulfilling the training needs of finished pharmaceutical manufacturers. Drawing on the authors` more than two decades of experience, the text offers hands-on training based on current approaches


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