How to Validate a Pharmaceutical Process

Häftad, Engelska, 2016

Av Steven Ostrove, USA) Ostrove, Steven (Ostrove Associates, Inc. Elizabeth, NJ

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How to Validate a Pharmaceutical Process provides a "how to� approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a pharmaceutical process. Understanding the "why� is critical to a successful and defensible process validation, making this book an essential research companion for all practitioners engaged in pharmaceutical process validation.

Thoroughly referenced and based on the latest research and literature
Illustrates the most common issues related to developing and implementing a sustainable process validation program and provides examples on how to be successful
Covers important topics such as the lifecycle approach, quality by design, risk assessment, critical process parameters, US and international regulatory guidelines, and more

Produktinformation

Utgivningsdatum2016-06-17
Mått152 x 229 x 14 mm
Vikt360 g
FormatHäftad
SpråkEngelska
SerieExpertise in Pharmaceutical Process Technology
Antal sidor218
FörlagElsevier Science
ISBN9780128041482

Tillhör följande kategorier

Tillverkningsteknik inom Naturvetenskap och teknik
Farmakologi inom Medicin

Dr. Ostrove has over 30 years of experience in validation compliance, quality assurance, and regulatory affairs. In addition, he has developmental and process expertise in mammalian cell culture and separation technology. His general pharmaceutical experience includes sterile techniques (Aseptic processing), Process Validation, Cleaning and Sterilization Validation, Packaging Systems, Process Development and Process Scale-up. He also has industry experience with the development and validation of PC and PLC-based computer control systems for the biotech and pharmaceutical markets, guidance on system optimization for CIP/SIP and has led teams for the review of all GMP documents starting with their preparation (e.g., protocols, SOPs, and validation master plans). Dr. Ostrove has worked on several consent degree remediation and audit teams and his experience covers both EU and US regulations. He is the author of the Elsevier short format book How to Validate a Pharmaceutical Process (Jun 2016, 9780128041482).

1. IntroductionSection I What is Process Validation and Why do Process Validation?2. Defining Process Validation3. Brief Review of the Regulations and Guidelines4. The Role of Change ControlSection II Stage I – Process Development5. Starting the Process Validation Program6. Equipment and Utility Qualification7. Dealing with Computers and Automation Validation8. Process DevelopmentSection II Process Qualification 9. The Process Validation Protocol 10. Dealing with DeviationsSection III Continued Process Verification 11. Collecting and Evaluating Production12. Use of Statistical Process Control – pPk, Pk, cPk, cPSection IV Other Related Activities13. Cleaning- Verification to Validation14. Facility Qualification