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Clean Technology for the Manufacture of Specialty Chemicals

Producing large quantities of waste is not only environmentally unacceptable, it is also not viable in economic terms. The chemical industry, particularly the speciality and pharmaceuticals sectors, is becoming increasingly aware of the advantages associated with clean technology, particularly in terms of competitive advantage and environmental benefits.||Bringing together an understanding of the concepts and values of clean technology by using case studies from some leading European countries, this book provides an insight into subjects such as catalysis; process intensification; and how to measure the "green" value of a process. It also highlights the role played by both the chemical and chemical engineering disciplines in the development of cleaner processes.||Clean Technology for the Manufacture of Speciality Chemicals will prove valuable reading for process development chemists and engineers, particularly those in the specialities and pharmaceuticals sectors, and will also be an important source of teaching material for the growing number of clean technology chemistry courses.

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Posted in books by kdsaggi on May. 20, 2008 // 06:54 | Comments (0)
Pharmaceutical Manufacturing Handbook: Regulations and Quality

Everything you need to ensure full compliance and superior quality control

With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines.

The team of expert authors, all familiar with the many issues involved in compliance and quality control, offer you advice based on their own firsthand experience in all phases of pharmaceutical manufacturing. The editor, who has more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.

* Among the key topics covered are:
* Enforcement of current good manufacturing practices
* Inspections by health regulatory agencies
* Creating and managing a quality management system
* Personnel training within pharmaceutical manufacturing
* Microbiology of non-sterile pharmaceutical manufacturing

Pharmaceutical manufacturing validation principles

Following the handbook's carefully developed guidelines and advice helps you ensure your company's full compliance and avoid potential costly pitfalls. This publication should be readily accessible to all scientists, engineers, and managers involved in pharmaceutical manufacturing.

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Posted in books by kdsaggi on May. 20, 2008 // 06:56 | Comments (0)
Pharmaceutical Manufacturing Handbook: Production and Processes

Everything you need to know to manufacture high-quality pharmaceuticals safely and efficiently

From the building of a facility to dosage and delivery forms to tablet production, this handbook covers the full range of topics to help you understand and apply the methods needed to manufacture drugs safely and efficiently. Thoroughly up to date, the handbook also examines the emerging role of nanotechnology in the development and manufacture of drugs and medical devices. Comprehensive in its presentation, this reference includes an entire section dedicated to the economics and business strategies of pharmaceutical manufacturing.

This handbook features contributions from a team of expert authors representing the manydisciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate,and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.

Among the key topics covered are:
* Radiopharmaceutical manufacturing
* Clean facility design, construction, and maintenance
* Controlled-release dosage forms
* Biodegradable nanoparticles
* Tablet production systems

Cyclodextrin-based nanomaterials in the pharmaceutical field

This publication serves as a hands-on reference for all scientists, engineers, and managers involved in pharmaceutical manufacturing, providing a basic primer for novices and detailing the latest discoveries and techniques for more experienced practitioners.

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Posted in books by kdsaggi on May. 20, 2008 // 06:57 | Comments (0)