Download or read book Plastic Containers for Pharmaceuticals written by Jack Cooper and published by . This book was released on 1974 with total page 204 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Plastic containers for pharmaceuticals testing and control written by Jack Cooper and published by . This book was released on 1974 with total page 204 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Plastic containers for pharmaceuticals testing and control written by Jack Cooper and published by . This book was released on 1974 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Plastic Packaging written by Otto G. Piringer and published by John Wiley & Sons. This book was released on 2008-06-25 with total page 632 pages. Available in PDF, EPUB and Kindle. Book excerpt: Plastics are the most important class of packaging materials. This successful handbook, now in its second edition, covers all important aspects of plastic packaging and the interdisciplinary knowledge needed by food chemists, pharmaceutical chemists, food technologists, materials scientists, process engineers, and product developers alike. This is an indispensable resource in the search for the optimal plastic packaging. Materials characteristics, additives and their effects, mass transport phenomena, quality assurance, and recent regulatory requirements from FDA and European Commission are covered in detail with ample data.

Download or read book Quality Testing and Quality Control of Pharmaceutical Packaging Materials written by G. Lürding and published by . This book was released on 1979 with total page 83 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Packaging of Pharmaceuticals and Healthcare Products written by Frank A. Paine and published by Springer Science & Business Media. This book was released on 2012-12-06 with total page 221 pages. Available in PDF, EPUB and Kindle. Book excerpt: As was the case with Charles Ross's Packaging of Pharmaceuticals published by the UK Institute of Packaging in 1975 it is assumed that the reader of this book already has a broad understanding of the basics of packaging. If not the Packaging Users Handbook and the Handbook of Food Packaging are recommended. The packaging needs of pharmaceuticals are different in degree only from those of other perishable products such as processed foods. Because the required action of a medication can be nullified by any deterioration in its active principles the protection required from its packaging is at least an order of magnitude greater than that needed by foods for example. Functional efficiency is therefore of prime importance. Conversely the need for the packaging to 'sell' the medication is much less, hence the graphics required need only provide the right 'image' for the product when presented for use in hospital or surgery. Even when on sale at the pharmacy the 'appeal' required is that of providing hygiene and confidence more than anything else. Thus, the textual requirements are paramount including traceability (batch numbers, date-coding etc) in case of recall; while striking appearance to attract customer attention is in lower key. And with the increase in malicious tampering nowadays recall is more frequent.

Download or read book Pharmaceutical Packaging Technology written by D. A. Dean and published by CRC Press. This book was released on 2005-07-12 with total page 459 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmaceutical packaging requires a greater knowledge of materials and a greater intensity of testing than most other packed products, not to mention a sound knowledge of pharmaceutical products and an understanding of regulatory requirements. Structured to meet the needs of the global market, this volume provides an assessment of a wide range of issues. It covers the entire supply chain from conversion of raw materials into packaging materials and then assembled into product packs. Integrating information from many drug delivery systems, the author discusses testing and evaluation and emphasizes traceability and the need to for additional safeguards.

Download or read book Guideline for Submitting Documentation for Packaging for Human Drugs and Biologics written by and published by . This book was released on 1988 with total page 44 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Qualit tspr fung und Qualit tssteuerung von pharmazeutischen Packmitteln written by Hans D. Ruthemann and published by . This book was released on 1979 with total page 51 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Quality testing and quality control of pharmaceutical packaging materials written by Hans D. Ruthemann and published by . This book was released on 1979 with total page 69 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Quality testing and quality control of pharmaceutical packaging materials written by and published by . This book was released on 19?? with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book High Altitude Testing and Evaluation of Liquid Pharmaceutical Glass and Plastic Bottles to Detect Leaks written by S. P. Singh and published by . This book was released on 2007 with total page 9 pages. Available in PDF, EPUB and Kindle. Book excerpt: This paper discusses the impact on package integrity of high-altitude shipments of glass and plastic bottles. High altitudes are encountered when trucks travel over mountain passes and when cargo and feeder aircraft transport packages in nonpressurized or partially pressurized cargo holds. This is the second research study conducted on liquid product shipments. The first was done on liquid hazardous material combination packaging. The testing of pharmaceutical packaging is critical since the integrity of the product may be compromised during shipping and handling. Current shipping tests performed in labs do not account for simultaneous pressure changes and vibration. This study shows that packages currently being used for shipments of liquid pharmaceuticals that are tested to existing ASTM and ISO shipping tests are often inadequate, and can result in a significant number of leakers. Testing under combined vibration and pressure is necessary to ensure integrity.

Download or read book Child resistant Packaging written by American Society for Testing and Materials and published by ASTM International. This book was released on 1976 with total page 113 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Evaluation list for defects in rubbert parts written by and published by . This book was released on 1977 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Quality assurance of pharmaceuticals a compendium of guidelines and related materials Volume 2 Good manufacturing practices and inspection written by World Health Organization and published by World Health Organization. This book was released on 2024-01-31 with total page 1354 pages. Available in PDF, EPUB and Kindle. Book excerpt: The GMP Compendium for Medical Products is a valuable resource for manufacturers, regulators, and other stakeholders involved in producing and distributing medical products. It covers various topics, from quality management systems to personnel hygiene, equipment validation, and complaint handling. The guidance provided is based on the latest scientific and technical knowledge and considers the evolving regulatory landscape and the challenges faced by the industry.

Download or read book Qualit tspr fung und Qualit tssteuerung von pharmazeutischen Packmitteln written by Werner Mässing and published by . This book was released on 1980 with total page 59 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Pharmaceutical Microbiological Quality Assurance and Control written by David Roesti and published by John Wiley & Sons. This book was released on 2020-01-02 with total page 594 pages. Available in PDF, EPUB and Kindle. Book excerpt: Relying on practical examples from the authors’ experience, this book provides a thorough and modern approach to controlling and monitoring microbial contaminations during the manufacturing of non-sterile pharmaceuticals. Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on statistical tools for risk assessment and trending of microbiological data Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on statistical tools for risk assessment and trending of microbiological data Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks