Description
Book SynopsisQuality assurance and good laboratory practices are becoming essential knowledge for professionals in all sorts of industries. This includes internal and external audit procedures for compliance with the requirements of good clinical, laboratory and manufacturing practices. Spanning chemical, cosmetic and manufacturing industries, Good Clinical, Laboratory and Manufacturing Practices: Techniques for the QA professional is aimed at: chemists, clinicians, ecotoxicologists, operation managers, pharmaceutical process managers, quality assurance officers, technicians and toxicologists. In addition sections on harmonisation of quality systems will be of value to safety, health and environment advisors. This comprehensive and high level reference will be an indispensable guide to research laboratories in academia and industry. Additional training material is also included.
Trade Review"This book should be essential reading for all those working QA" * Pharmazie in Unserer Zeit, Markus Veit, Kaufering. *
Those involved in quality assurance and control could use the book as a reference guide and as a source of best-practice methodology to set up, operate, monitor and interpret a quality system....exceptionally well-presented.....s a well-structured, comprehensive and easy-to-read book.In nearly 30 years as an analytical chemist and quality professional, I have not come across a book that is a must-read, but this certainly is. * Chemistry World, November 2007, 74 (J A Day) *
Table of ContentsChapter 1: Introduction to Part 1 - GCP; Chapter 2: The Protocol, Case Report Form & Initial Documentation - Quality Assurance Involvement & Common Problems; Chapter 3: Standard Operating Procedures in the GCP Environment; Chapter 4: Preparing for Regulatory Inspections of Company Pharmacovigilance Systems & Practices in the European Union & United States; Chapter 5: Investigator, Sponsor & Contract Research Organisation Audits; Chapter 6: Data Audits; Chapter 7: Research Ethics Committees; Chapter 8: GCP/GMP Interface, Investigational Product Accountability; Chapter 9: Monitoring & Quality Control; Chapter 10: Phase I Healthy Volunteer Studies; Chapter 11: Clinical Laboratories; Chapter 12: Introduction to Part 2 - Good Laboratory Practice; Chapter 13: Quality Assurance in GLP; Chapter 14: The Master Schedule Index; Chapter 15: Study Plans & Their Audits; Chapter 16: SOPs for GLP Work; Chapter 17: Inspections - Procedural, Process & Facility; Chapter 18: Report and Data Audits; Chapter 19: Quality Assurance & Contract Research Organisations; Chapter 20: Quality Assurance & Pharmacology; Chapter 21: Application of GLP in Analytical Chemistry; Chapter 22: GLP in Drug Metabolism & Pharmacokinetics; Chapter 23: Issues of Quality in Pathology; Chapter 24: GLP in Eco-toxicology and Field Studies; Chapter 25: Animal Health; Chapter 26: Introduction to Part 3 - Good Manufacturing Practice; Chapter 27: Standard Operating Procedures (Specific to GMP); Chapter 28: Release of Bulk & Filled Finished Product; Chapter 29: Good Manufacturing Practice for Investigational Medicinal Products; Chapter 30: Chemical Analysis; Chapter 31: GMP for Sterile Products; Chapter 32: Statistics for QA Auditors of GLP and GCP Studies; Chapter 33: The Use of Statistics in Research Quality Assurance; Chapter 34: Supplier Auditing (GMP); Chapter 35: Centralised Supplier Audits (GLP); Chapter 36: Document Control from Concept to Archiving; Chapter 37: Computing & GXP's; Chapter 38: QA Developing A Regulatory Compliance Training Strategy; Chapter 39: Training & Staff Records for GXP; Chapter 40: Integrating Quality Systems (GCP, GLP, GMP, ISO 9000, 14001, 18001 & 17025
