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AVANCE Beginner's Level Guides and Tutorials
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English (version 4) |
German (version 4) |
French (version 3) |
Spanish (version 3) |
Italian (version 3) |
The manual is currently available in the following languages for XWIN-NMR users:
English |
German |
French |
Spanish |
Italian |
The 1D and 2D Experiments Step-by-Step Tutorials were written for AVANCE systems running TopSpin and should be used as a guide through the set up process for some experiments. The success of running the experiments in these manuals are under the assumption that all parameters have been entered in to the prosol table.
There are two tutorials available, one for basic experiments and one for advanced experiments:
1D and 2D Experiments Step-by-Step Tutorial: Basic Experiments
1D and 2D Experiments Step-by-Step Tutorial: Advanced
Experiments
The AVANCE NMR Hardware Guides are intended to serve as introductory guides to AVANCE spectrometer hardware. They have been written primarily for operators who wish to have basic information regarding the system components and how they interact with one another. They are not intended as service guides and will in no way equip the reader to carry out any service or repairs. However there is an ever increasing desire for users to understand the underlying hardware so they can:
At a more fundamental level there is a widely held belief that as spectrometers become more and more complex the operators have less and less of an understanding of the spectrometer hardware.These guides are intended to help reverse that trend. It is also hoped that the reader will come to appreciate some of the design issues involved in modern spectrometer systems.
There are two guides available, one for AVANCE AV and AVANCE II systems, and one for the new AVANCE III systems. Currently the guides are only available in English:
AVANCE AV/II |
AVANCE III |
Many chemical, pharmaceutical, biotech companies and laboratories must comply with regulatory requirements or are planning to organize their activity according to federal or international quality management standards. One of the best known standards is GLP, or Good Laboratory Practice.
In the U.S.A. GLP documents are issued by the Food and Drug Administration (FDA). The FDA GLP regulations are enforceable under the Federal Food, Drug and Cosmetic Act, and apply to non-clinical laboratory studies that are submitted to the FDA in support of an application for a research or marketing permit.
FDA regulations have also been taken on by the Council of the OECD countries, who then advised the corresponding health ministers to adopt GLP. Laws have then been formulated to cover this matter in each country, i.e., to regulate the way chemical substances are dealt with and with instrumentation in non-clinical laboratories.
Based on its official definition, GLP is concerned with the organizational processes and conditions under which laboratory studies are:
GLP data are intended to promote the quality and validity of test data.
The GLP Requirements User Guide provides an overview of GLP for laboratory managers (LM’s), and those people responsible in applying GLP principles to the above mentioned conditions in an environment with NMR systems.