Compatibility of Pharmaceutical Solutions and Contact Materials: Safety Assessments of Extractables and Leachables for Pharmaceutical Products | Date: 27 April 2011, 09:06
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Review
"The analogy of extractables and leachables to the bogeyman hiding in the closet is so true and telling, whether experienced with leachable studies or not the issues are well communicated. Nomenclature is established, in the author?s vernacular, which describes pharmaceutical contact materials and key terms enabling a clear understanding of the objectives of compatibility assessments. Excellent examples of extractables studies, correlations and risk assessments are given and the classification of extraction strategies puts into perspective the purpose for acquiring the data. The appendix listing materials and their associated extractables is a valuable reference tool for chemists, toxicologists and regulators involved with qualifying contact materials used with pharmaceutical products. This is a comprehensive and practical guide for both the novice and the knowledgeable. A great read!" --Diane M. Paskiet, Associate Director of Scientific Affairs, West Pharmaceutical Services
Product Description
Compatibility of Pharmaceutical Products and Contact Materials
Dennis Jenke
Important safety aspects of compatibility for therapeutic products and their manufacturing systems, delivery devices, and containers
Compatibility of Pharmaceutical Products and Contact Materials helps pharmaceutical, toxicology, analytical, and regulatory affairs professionals assess the safety of leachable and extractable chemicals associated with drug product packaging, manufacturing systems, and devices. The most comprehensive resource available, its coverage includes the strategies, tactics, and regulatory requirements for performing safety assessments, along with the means for interpreting results.
Structured around a logical framework for an extractables and leachables safety assessment and closely linked to the pharmaceutical product development process, Compatibility of Pharmaceutical Products and Contact Materials directly addresses the fundamental questions of "what activities need to be performed to completely, efficiently, and effectively address the issue of product safety from an extractables and leachables perspective?" and "when do the various required activities need to be performed?" Specifically, the chapters describe:
Pertinent regulations and practical ways to meet guidelines
Coordinating manufacturing, storage, and delivery systems development and qualification with therapeutic product development
Materials characterization and the materials screening process
Component and/or system qualification (illustrated by several case studies)
Performing validation/migration studies and interpreting and reporting the results
Creating a product registration dossier and putting it through regulatory review
Product maintenance (Change Control) from an extractables and leachables perspective
Likely future developments in extractables and leachables assessment
Additionally, the book's appendix provides a database, including CAS registry numbers, chemical formulas and molecular weights of extractable/leachable substances that have been reported in the chemical literature.
Detailing the interconnected roles played by analytical chemistry, biological science, toxicology, and regulatory science, Compatibility of Pharmaceutical Products and Contact Materials supplies a much-needed, comprehensive resource to all those in pharmaceutical product or medical device development.
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