Good Distribution Practice: A Handbook for Healthcare Manufacturers and Suppliers, Volume 2 (single user digital version)
- Published
- Sep 2019
- ISBN
- 19781942911395
- Pages
- 420
- PDA Item Number
- 18062
- Format
- PDF Single user
- Member Price
- $210.00
- Nonmember Price
- $259.00
- Government Price
- $210.00
Please sign in or become a member to purchase items from the PDA bookstore.
Following an introduction to the subject of Good Distribution Practice (GDP), in the second volume, dive into supply-chain risk mitigation, serialization, and packaging as it relates to risk assessments.
This text and its companion Volume 1 will help drive down costs and improve efficiency.
Available to download. Prior to purchase please view the download instructions and Terms of Usage
Format: PDF (1 file 16.9 MB)
Table of Contents
Table of Contents:
Click here to download >>>Detailed Table of Contents
Foreword by Lea Joos
Section I Introduction
- Introduction by Siegfried Schmitt
Section 2 De-Risking the Supply Chain
- Risk Management and Supply Chain Security by Tony Pelli and Jim Yarbrough
- Prioritising and Managing Supply Chain Risks by Catherine Geyman
- Controlled Distribution Systems by Martine Zimmermann
Section 3 Serialisation and Packaging in Practice
- Serialisation - Preventing Falsification of Pharmaceutical Products by Fritz Roeder, Klaus Egner, Michael Hell
- Passive Packaging for the Temperature Controlled Transport of Healthcare Products by Stephen Brabbs, Srinivas Cherukupalli, Lawrence M. Knorr and Daniel Wisnom
- Active Unit Load Device Shipping Containers by Chris Fore
- Passive Thermal Packaging Solutions for Air Freight by Nicolas Buser
- Extractables and Leachables of Container and Packaging Systems for Pharmaceutical Products by Xiaochun Yu
- Serialisation Around the World by Wipotec-ocs
Section 4 Appendix
- Appendix Guide to Good Distribution Practice of Medicinal Products for Human Use by Health Products Regulatory Authority Ireland
About the Authors
About the Editor
Dr Siegfried Schmitt, Vice President Technical at PAREXEL Consulting has 30 years' experience in the regulated healthcare industry. He has previously held positions in industry as Senior Production Chemist with Roche and global Quality Director with GE Healthcare and as Validation Manager with Raytheon and Senior Lead Consultant with ABB.
He has consulted with many clients on four continents, particularly on the design and operation of compliant, yet agile and effective quality systems.