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Productivity Press
16 June 2017
This book addresses the rapidly emerging field of Knowledge Management in the pharmaceutical, medical devices and medical diagnostics industries. In particular, it explores the role that Knowledge Management can play in ensuring the delivery of safe and effective products to patients. The book also provides good practice examples of how the effective use of an organisation's knowledge assets can provide a path towards business excellence.
Edited by:   Nuala Calnan (School of Chemical and Pharmaceutical Sciences Dublin Institute of Technology Dublin Ireland), Martin J Lipa (Merck & Co. Inc., West Point, PA, USA), Paige E. Kane, Jose C. Menezes (IST - Bioengineering Department, Lisbon University, Lisbon, Portugal)
Imprint:   Productivity Press
Country of Publication:   United States
Dimensions:   Height: 235mm,  Width: 156mm, 
Weight:   1.066kg
ISBN:   9781498750479
ISBN 10:   1498750478
Series:   Biotechnology and Bioprocessing
Pages:   523
Publication Date:   16 June 2017
Audience:   General/trade ,  College/higher education ,  Professional and scholarly ,  ELT Advanced ,  Primary
Format:   Hardback
Publisher's Status:   Active
MAKING THE CASE FOR KNOWLEDGE EXCELLENCE IN THE BIOPHARMACEUTICAL INDUSTRY Why KM is Good Business P.K. Yegneswaran, Michael P. Thien, and Martin J. Lipa Theory of Knowledge Management Stefanie N. Lindstaedt, Paul Czech, and Angela Fessl Knowledge Management - A Japanese Perspective Yukio Hiyama Accelerating the Opportunity for the Pharmaceutical Industry through KM Lauren Trees and Cindy Hubert INTRODUCTION: PERSPECTIVES ON KNOWLEDGE Who Moved My Facts? Dave deBronkart Valuing Knowledge at Swissmedic - A Regulatory Agency's Perspective Michael Renaudin and Hansjurg Leuenberger A Regulatory Perspective: Generating New Knowledge from Dada: Protecting the Patient by Exploring What is Known About Quality Defects and Product Recalls Nuala Calnan and Anne Greene A Perspective from NASA: Knowledge Services and Accelerated Learning in NASA - The REAL Knowledge Approach Ed Hoffman and Jon Boyle An Academic Perspective: Knowledge Management The Orphan Enabler - Enabling ICH Q10 Implementation Nuala Calnan, Anne Greene, and Paige E. Kane An Academic Perspective: Effective Knowledge Assessment Mohamed AF Ragab and Amr Arisha Knowledge Management and the Evolving Regulatory Process Bill Paulson and Paige E. Kane INTRODUCTION: PRACTICES, PILLARS AND ENABLERS: FOUNDATIONS FOR SUCCESSFUL KM The House of Knowledge Excellence: A Framework for Success Paige E. Kane and Martin J. Lipa A Holistic Approach to Knowledge Management: Pfizer Global Supply Paige E. Kane and Alton Johnson KM Evolution at Merck: Managing Knowledge in Merck Manufacturing Division Martin J. Lipa and Jodi Schuttig Integrating Knowledge Management with Quality Management Systems to Manufacture Pharmaceuticals Consistently and Reliably Barbara Allen Working with the IS/IT Function to Set Up Your Knowledge Management Project for Success Joseph Horvath Knowledge Management Implementation: A Guide to Driving Successful Technology Realization Doug Redden INTRODUCTION: PRACTICES AND CASE STUDIES IN ENABLING KNOWLEDGE FLOW Let's Talk About Knowledge Management: Learning from the Library of Alexandria Disaster Sandra Bush and Matthew Neal Rapid and Robust Product Development Powered by Knowledge Management Capability Anando Chowdhury Knowledge Management Case Study: Using Near Real-Time Data Analytics and Performance Metrics to Ensure a Robust and Resilient Supply Chain Eda Ross Montgomery, Mani Sundararajan, David Lowndes, and Gabriele Ricci Knowledge Management Elements in Support of Generation of CMC Regulatory Documentation Beth Junker A People Approach to Managing Knowledge: Why Do You Come to Work and Who Are You Working For? Sian Slade and Catherine Shen Developing a Lessons Learned Process - Where Lessons Are Learned: A Case Study of Pfizer Pharmaceutical Sciences Phil Levett Capturing Critical Process and Product Knowledge: The Development of a Product History File Dave Reifsnyder, Kayhan Guceli, and Kate Waters Communities of Practice: A Story About the VTN and the Value of Community Renee Vogt, Joseph Schaller, and Ronan Murphy Identification of Critical Knowledge: Demystifying Knowledge Mapping Paige E. Kane and Chris Smalley The Practical Application of a User-Facing Taxonomy to Improve Knowledge Sharing and Reuse Across the Biopharmaceutical Product Lifestyle: A Case Study Adam Duckworth, Vince Capodanno, and Thomas Loughlin Knowledge Based Product and Process Lifecycle Management for Legacy Products Marco Strohmeier, Christelle Pradines, Francisca F. Gouveia, and Jose C. Menezes

Nuala Calnan, PhD has over 20 years' experience in the pharmaceutical industry and is currently an adjunct Research Fellow with the Pharmaceutical Regulatory Science Team at DIT, Ireland, where she leads a number of patient focused regulatory science research projects at Masters and PhD level. Dr. Calnan's focus is on the integration of Knowledge Excellence, Operational Excellence, & Cultural Excellence in delivering enhanced quality outcomes for the patient and has led a recent Irish Industry research study in this field examining the Product Recall and Quality Defect data at the Irish medicines regulator, HPRA. She is currently a member of the St. Gallen University led team who were awarded a one-year research grant by FDA examining the role of Quality Metrics in determining risk-based inspection planning. Dr. Calnan also works closely with industry in the areas of Quality Excellence and Metrics, Data Integrity and Quality Culture development. Dr. Calnan co-leads the ISPE Quality Culture Team and the ISPE/ PQLI Task Team on Knowledge Management. Martin Lipa is an Executive Director in Merck Manufacturing (MMD) and leader of the MMD Knowledge Management Center of Excellence (Knowledge Management CoE). For the past 8 years he has worked to create Knowledge Management strategy for Merck Manufacturing and other functions across the Merck enterprise and to build capabilities and competency in Knowledge Management as an enabler of the company's strategy. Lipa has over 20 years' experience in the biopharmaceutical industry. Prior to focusing on Knowledge Management, he started his career as a Technical Operations engineer and then progressed through roles in shop floor automation, computer systems validation, new GxP facility startup, project management and clinical supplies. He is also a certified LSS Black Belt and specializes in change management techniques. Lipa is a recognized industry Knowledge Management thought leader and has helped organize multiple Knowledge Management conferences. He has also published industry specific works and features as a regular speaker sharing his experience and learnings. Paige E. Kane, CPIP, is a Director in the Merck Manufacturing Division Knowledge Management Center of Excellence. In addition she is a regulatory science researcher at Dublin Institute of Technology in Dublin, Ireland where she is pursuing a PhD focusing in the realization of the ICH Q10 enabler - Knowledge Management. For the past 10 years, she has been involved in developing and implementing Knowledge Management Strategies for Wyeth and Pfizer Global Supply with a strong focus on people, collaboration, and processes. Kane has over 25 years' experience working in a regulated environment (including Genetics Institute, Wyeth, Pfizer, Monsanto, and the US Government). Kane has been responsible for developing and implementing Quality Systems for GLP, GCP and GMP, as well as Computer System Validation programs. In addition, she provided leadership and Subject Matter Expertise for multiple biotech startups in the US and Europe. Kane is the Co-Chair of the ISPE/ PQLI Task Team on Knowledge Management.and serves locally as co-chair of the Boston ISPE Student Development Committee. Jose Menezes, PhD is founder and director of one of the earliest Pharmaceutical Engineering programs in Europe and a pioneer on the use of PAT and QbD tools in bioprocessing. He is the recipient of a Presidential Award for Excellence in University-Industry collaborations. Dr. Menezes is a Professor at the University of Lisbon since 2005. He has published extensively on the subject of manufacturing sciences and technologies applied to pharma and biotech products. He earned Chemical Engineering BSc and MSc degrees and a PhD in Bioengineering from ULisbon. He worked for Ciba-Geigy in Switzerland and the nuclear industry also in Switzerland, before embarking on an academic career. During his 20 years at ULisbon, he spent multiple sabbatical periods in industry at different pharma companies in Europe, where he built, trained or managed several PAT and QbD teams. He is an active member of several societies and a Senior Member of AIChE, ISPE, PDA and IFPAC among other organizations. Dr. Menezes co-founded 4Tune Engineering Ltd in 2004 - an award-winning ISO 9001:2008 engineering services company - developing and implementing worldwide state-of-the-art manufacturing sciences and technologies solutions, to deliver quality risk management and excellence in corporate Knowledge Management over life-cycle.

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