304 pages | 66 B/W Illus.
This Second Edition is an essential guide to preparing for FDA pre-approval inspections—taking into account current trends in FDA expectations and inspection activities, such as the GMPs of the 21st Century, quality systems-based approach to inspections, risk-based inspections, quality by design, process analytical technology, design space, etc. The goal of this book is to help organizations gain rapid regulatory approval.
Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition:
Introduction/Preface. Pre-Approval Inspection: A Historical Overview. Recent Trends in Domestic and International Pre-Approval Inspections. The Implications of the Quality Systems, Risk Based Inspections and 21st Century GMPs to Preparing for FDA Pre-Approval Inspections. Preparing for FDA Pre-Approval Inspections Similarities and Differences between Center for Biologics Evaluation and Research (CBER) / Center for Drug Evaluation and Research (CDER). The GMP Risk Assessment, Guidance for Preparing for Pre-Approval Inspections, Traditional and Non-Traditional. The Product Development Drill, the Importance of Good Science, Stability Data, Scale Up, and Validation to Successfully Passing a Pre-Approval Inspection. The History of Development Documents: Guidance for Preparation in Light of Recent Trends. Computer Validation Systems Validation during the Drug Development Process. The Use of Audits during the Drug Development Process to Assure a Successful Pre-Approval Inspection. The Consequence of a Poor Product Development Process and Failing a Pre-Approval Inspection.