GAMP 5

GAMP 5

Author: Sion Wyn

Publisher:

Published: 2008

Total Pages: 0

ISBN-13: 9781931879613

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GAMP 5 provides pragmatic and practical industry guidance to achieve compliant computerized systems fit for intended use in an efficient and effective manner. This technical document describes a flexible risk-based approach to compliant GxP regulated computerized systems, based on scalable specification and verification. It points to the future of computer systems compliance by centering on principles behind major industry developments such as PQLI; ICH Q8, Q9, Q10; and ASTM E2500. This revolutionary Guide addresses the entire lifecycle of an automated system and its applicability to a wide range of information systems, lab equipment, integrated manufacturing systems, and IT infrastructures. It contains new information on outsourcing, electronic batch recording, end user applications (such as spreadsheets and small database applications), and patch management.


Computer System Validation and GAMP 5

Computer System Validation and GAMP 5

Author: Vonlynx Solutions LLC

Publisher: Independently Published

Published: 2020-12-19

Total Pages: 120

ISBN-13:

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The purpose of this book is to help you understand how computerized systems are validated using the GAMP5framework. The information will be presented in a project life cycle format. This will give you a solid idea howComputerized System Validation projects are conducted. This book is suited for anyone new to Computer SystemsValidation. It is written in a simple manner and can serve as starter guide which includes many high-level sample templates and illustration.


Pharmaceutical Computer Systems Validation

Pharmaceutical Computer Systems Validation

Author: Guy Wingate

Publisher: CRC Press

Published: 2016-04-19

Total Pages: 773

ISBN-13: 1420088955

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Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements for computer systems, the text extensively reviews regulations of pharmaceuticals, healthcare products, blood processing, medical devices, clinical systems, and biotechnology. Ensuring that organizations transition smoothly to the new system, this guide explains how to implement the new GMP paradigm while maintaining continuity with current practices. In addition, all 24 case studies from the previous edition have been revised to reflect the new system.


International IT Regulations and Compliance

International IT Regulations and Compliance

Author: Siri H. Segalstad

Publisher: John Wiley & Sons

Published: 2008-11-20

Total Pages: 338

ISBN-13: 9780470721834

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Standards, technologies, and requirements for computer validation have changed dramatically in recent years, and so have the interpretation of the standards and the understanding of the processes involved. International IT Regulations and Compliance brings together current thinking on the implementation of standards and regulations in relation to IT for a wide variety of industries. The book provides professionals in pharmaceutical and semiconductor industries with an updated overview of requirements for handling IT systems according to various Quality Standards and how to ?translate? these requirements in the regulations.


Data Integrity in Pharmaceutical and Medical Devices Regulation Operations

Data Integrity in Pharmaceutical and Medical Devices Regulation Operations

Author: Orlando Lopez

Publisher: CRC Press

Published: 2016-11-03

Total Pages: 268

ISBN-13: 1315349973

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Data integrity is fundamental in a pharmaceutical and medical devices quality system. This book provides practical information to enable compliance with data integrity, while highlighting and efficiently integrating worldwide regulation into the subject. The ideas presented in this book are based on many years’ experience in regulated industries in various computer systems development, maintenance, and quality functions. In addition to case studies, a practical approach will be presented to increase efficiency and to ensure that the design and testing of the data integrity controls are correctly achieved.


How to Cake It

How to Cake It

Author: Yolanda Gampp

Publisher: HarperCollins

Published: 2017-10-24

Total Pages: 552

ISBN-13: 1443453900

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From Yolanda Gampp, host of the massively popular, award-winning YouTube sensation “How to Cake It,” comes an inspiring “cakebook” with irresistible new recipes and visual instructions for creating spectacular novelty cakes for all skill levels. On her entertaining YouTube Channel, “How to Cake It,” Yolanda Gampp creates mind-blowing cakes in every shape imaginable. From a watermelon to a human heart to food-shaped cakes such as burgers and pizzas—Yolanda’s creations are fun and realistic. Now, Yolanda brings her friendly, offbeat charm and caking expertise to this colorful cakebook filled with imaginative cakes to make at home. How to Cake It: A Cakebook includes directions for making twenty-one jaw-dropping cakes that are gorgeous and delicious, including a few fan favorites with a fresh twist, and mind-blowing new creations. Yolanda shares her coveted recipes and pro tips, taking you step-by-step from easy, kid-friendly cakes (no carving necessary and simple fondant work) to more difficult designs (minimal carving and fondant detail) to aspirational cakes (carving, painting and gum-paste work). Whatever the celebration, Yolanda has the perfect creation, including her never before seen Candy Apple Cake, Party Hat, Rainbow Grilled Cheese Cake, Toy Bulldozer Cake and even a Golden Pyramid Cake, which features a secret treasure chamber! Written in her inspiring, encouraging voice and filled with clear, easy-to-follow instructions and vibrant photos, How to Cake It: A Cakebook will turn beginners into confident cake creators, and confident bakers into caking superstars!


Pharmaceutical Technology And Process

Pharmaceutical Technology And Process

Author: Dr. Abhinandan Ravsaheb Patil

Publisher: AG Publishing House (AGPH Books)

Published: 2022-09-12

Total Pages: 224

ISBN-13: 9395468807

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Recent materials, process development, and drug delivery strategies are explored through the Challenges faced by Pharmaceutical Technology. Techniques for the statistical formulation optimization, the Quality by design along with process analytical technologies, and the use of a wide range of pharmaceutical biomaterials—from natural polymers and synthetic polymers to modified-natural polymers, bioceramics, as well as other bioinorganica—are all covered in detail. As the area of pharmaceuticals continues to expand at a fast pace, this book provides a comprehensive overview of the procedures, formulation innovations, investigations, and exploitation of pharmaceutical biomaterials used in the production of pharmacological dosage forms. From the first stages of medication development to production, methods and technology, rules and regulations, and finally, marketing, this book covers it all. Everything an undergraduate student of pharmacy or pharmaceutical sciences needs to know about pharmaceuticals is covered in this book, from active pharmaceutical components through the manufacture of different dosage forms and the associated chemistry. This book details the process through which a certain medicine was developed, tested, and ultimately brought to market. It describes all drugs that are discovered, how they work, the challenges of experimenting with them, why different dosages work, how quality is ensured, and the responsibilities of regulatory organizations. Quality assurance, product security, medicine counterfeiting and misuse, and pharmaceuticals' potential for the future are all discussed in depth.


Sterile Manufacturing

Sterile Manufacturing

Author: Sam A. Hout

Publisher: CRC Press

Published: 2021-07-04

Total Pages: 148

ISBN-13: 1000406121

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This book highlights key ideas and factors to coach and guide professionals involved in learning about Sterile Manufacturing and operational requirements. It covers regulations and guidelines instituted by the FDA, ISPE, EMA, MHRA, and ICH, emphasizing good manufacturing practice and inspection requirements in the manufacturing of medicinal products. Additionally, this book provides the fundamentals of aseptic techniques, quality by design, risk assessment, and management in support of sterile operations applications. It creates a link to the implementation of business practices in drug manufacturing and healthcare and forms a correlation between design strategies including a step-by-step process to ensure reliability, safety, and efficacy of healthcare products for human and animal use. The book also provides a connection between drug production and regulated applications by offering a review of the basic elements of sterile processing, and how to remain viable with solid strategic planning. The book is a concise reference for professionals and learners in the field of sterile operations that governs primarily, pharmaceutical and medical device space, but can also extend to food and cosmetics that require clean (aseptic) manufacturing applications. It also helps compounding pharmacists and GMP inspectors and auditors.