Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing
This book contains both the theory and practice of risk management (RM) and provides
the background, tools, and application of risk in pharmaceutical and biologics
manufacturing and operations. It includes case studies and specific examples of use of RM
for biological and pharmaceutical product manufacture.
The book also includes useful references and a bibliography for the reader who wishes
to gain additional knowledge in the subject. It aids in assisting both industry and
regulatory agencies to implement compliant and effective risk management approaches, and
includes case studies to help with understanding.
1 Introduction and Background Hal Baseman and A. Hamid Mollah
2 Risk Management Tools Mark Walker and Tom Busmann
3 Risk Management: Regulatory Expectation, Risk Perception, and Organizational
Integration Mike Long
4 Statistical Topics and Analysis In Risk Assessment Mike Long
5 Quality by Design Bruce Davis
6 Process Development and Clinical Manufacturing Karen Ginsbury
7 Points to Consider for Commissioning and Qualification of Manufacturing Facilities
and Equipment Hal Baseman and Mike Bogan
8 Quality Risk Management in Process Lifecycle Validation A. Hamid Mollah and Scott
Bozzone
9 Aseptic Processing: One James Agalloco and James Akers
10 Aseptic Processing: Two Edward C. Tidswell
11 Pharmaceutical Product Manufacturing Marlene Raschiatore
12 Quality Risk Management in Biopharmaceutical Manufacturing Ruhi Ahmed and Tom Genova
13 Risk Based Change Control Bill Harclerode, Bob Moser, Jorge Ferreira, and Christophe
Noualhac Index
416 pages, Hardcover