Process Validation in Manufacturing of Biopharmaceuticals

ISBN-13: 9780367697624 / Twarda / 2023 / 552 str.

Opis

The fourth edition of Process Validation in Manufacturing of Biopharmaceuticals is a practical and comprehensive resource illustrating the different approaches for successful validation of biopharmaceutical processes.

Spis treści

1. The Evolution of Modern Process Validation: Commentary on the U.S. Food and Drug Administration’s 2011 Guidance for Industry, Process Validation Principles and Practices

Hal Baseman

2. Applications of Failure Modes and Effects Analysis to Biotechnology Manufacturing Processes

Robert J. Seely and John Haury

3. Process Characterization

James E. Seely

4. Scale-Down Models for Microbial and Mammalian Cell Culture Processes: Approaches and Applications

Ravali Raju et al.

5. Scale-Down Models for Purification Processes: Approaches and Application

Arch Creasy et al.

6. Principles of Quality Risk Management for Validation

Tiffany Baker and Patrick Mains

7. Lifespan Studies for Chromatography and Filtration Media

Anurag S. Rathore and Gail Sofer

8. Analytical Test Methods for Well-Characterized Biological and Biotechnological Products

Nadine Ritter and John McEntire

9. Adventitious Agents: Concerns and Testing for Biopharmaceuticals

Raymond W. Nims et al.

10. Biotech Facility Design for Validation

Phil DeSantis

11. Process Validation at Contract Manufacturing Organizations: Approaches, Incentives, Benefits, and Risks

Maria Wik and Scott Rudge

12. Validation of a Filtration Step

Jennifer Campbell et al.

13. Validation of Continuous Bioprocesses

Marc Bisschops and Mark Schofield

14. Role of Multivariate Analysis in Process Validation

Anurag S. Rathore and Vishwanath Hebbi

15. Process Development for Plasmid DNA Production

Frank Agbogdo et al.

O autorze

ANURAG S. RATHORE is an Institute Chair Professor at the Department of Chemical Engineering, Indian Institute of Technology, Delhi, India. He is also the Coordinator for the DBT COE for Biopharmaceutical Technology. His areas of interest include process development, scale-up, technology transfer, process validation, biosimilars, continuous processing, medical image analysis, process analytical technology and quality by design. He is presently serving as the Editor-in-Chief of Preparative Biochemistry and Biotechnology and Associate Editor for Journal of Chemical Technology and Biotechnology. He also serves on the Editorial Advisory Boards for Biotechnology Progress, Biotechnology Journal, Electrophoresis, BioPharm International, Journal of Chromatography B, Journal of Chromatography Open, Pharmaceutical Technology Europe, and Separation and Purification Reviews. Dr. Rathore has edited books titled Preparative Chromatography for Separation of Proteins and Peptides (2017), Quality by Design for Biopharmaceuticals: Perspectives and Case Studies (2009), Elements of Biopharmaceutical Production (2007), Process Validation (2005), Electrokinetic Phenomena (2004), and Scale-up and Optimization in Preparative Chromatography (2003). He has a Ph.D. in Chemical Engineering from Yale University.

HAL BASEMAN is the Chief Operating Officer at ValSource Inc., a consulting services firm.　 Hal has held various positions in the biopharmaceutical manufacturing and consulting industry and has been involved in sterile product manufacturing for over 45 years.　 He is the past Chair of the PDA Board of Directors, the past Co-chair of PDA Science Advisory Board, past Chair or Lead on several PDA groups and efforts, including the PDA Process Validation Interest Group, the task forces for PDA Technical Reports on Process Validation, Aseptic Process Simulation, and Quality Risk Management, and the PDA Aseptic Processing Points to Consider.　　 He is currently a member of the PDA TRI (Training and Research Institute faculty, Co-lead for the Kilmer Conference Regulatory Innovation Collaboration team, Chair of the SfSAP (Society for Sterility Assurance Professionals) Aseptic Processing Team, and Co-chair of the PDA Annex 1 revision response team.　 Hal has presented and published numerous articles and book chapters on topics related to sterile product manufacturing, risk management, and validation. He has edited books on Process Validation and Quality Risk Management. Hal holds a Bachelor of Science Degree in Biology from Ursinus College and a Master of Business Administration in Management from La Salle University.

Dr. Scott Rudge is a Principal Consultant and a member of the Syner-G team since January 2023. He is an experienced pharmaceutical professional with 33 years of progressive experience directing Process Engineering, Process Development, Product Development and overall Pharmaceutical Operations. Scott was a co-founder of RMC Pharmaceutical Solutions in 2004, which was acquired by SynerG Biopharma Group in January, 2023. Scott has built and led several organizations in the biopharmaceutical industry, including process engineering, process development and product development teams at Synergen, Amylin Pharmaceuticals and FeRx, where he reported to the CEO. Ultimately, Scott formed his own consulting company, RMC Pharmaceutical Solutions with the vision to provide product development services to biotech and pharmaceutical companies of all sizes and all stages of development. Scott has remained active as a thought leader and innovator in biotechnology and pharmaceutical development. Scott is a co-author on the award winning textbook "Bioseparation Science and Engineering", co-author on the new chapter in Perry’s "Chemical Engineering Handbook" on Biotechnology, co-editor on the CRC "Process Validation in Manufacturing of Biopharmaceuticals", and has been a reviewer for the National Academy of Science’s ten year strategic goals for separation sciences in 2020, in addition to many publications and patents. Scott earned his B.S. in Chemical Engineering from Worcester Polytechnic Institute and his M.S. and Ph.D in Chemical Engineering from Purdue University.