Dewey Decimal Classification and Relative Index [Hardcover] - DDC 23 : 4-Volume Set ; 2011 : ( ISBN - 13 : 978-1-910608-81-4 ) ; ( ISBN - 10 : ISBN-10: 1910608815 )\ English \ Sistema de Classificação Decimal Dewey DDC23

DDC 23 is here!

The new print edition of the Dewey Decimal Classification, DDC 23, is now available in the Americas. The DDC print edition is scheduled for delivery to locations outside the Americas in July 2011. Highlights of the new edition include several major changes held for simultaneous publication in the print and Web versions of the DDC plus many interim updates already distributed to users in WebDewey 2.0.

Place your order today!

We are now accepting orders for DDC 23. Orders are scheduled for delivery to the Americas now, and to locations outside the Americas in July 2011.

Dedicated to Dewey users worldwide, DDC 23 features:

- Many new topics and significant updates to selected fields
- Numbers informed by interaction with the worldwide community of Dewey users
- A complete overhaul to the representation of groups of people
- Revisions to several standard subdivisions
- Elimination of dual headings and unbalanced spans
- A minimal price increase

As a result, DDC 23:

- Better reflects the changing world
- More accurately reflects regional differences around the world
- Greatly increases classifier efficiency
- Is more intuitive for the way classifiers work

DDC 23 also features:

- New provisions in 004-006 Computer science and elsewhere to reflect changes in technology
- Updates to provisions for the Orthodox Church and Islam in 200 Religion
- Improved provisions in 340 Law for legal systems based on civil law
- Significant updates to 370 Education resulting in an improved international framework for levels of education, kinds of schools, policy issues and specific subjects in primary education
- Updated provisions for food and clothing
- Updates to 740 Graphic arts and decorative arts
- A new location and expanded development for cinematography and videography at 777
- Significant expansions throughout 796 Athletic and outdoor sports and games
- Significant expansions in Table 2, with parallel provisions in 930-990, for the ancient world, Italy, - Switzerland, Sweden, Finland, Turkey, Indonesia, Vietnam and Canada
- Updated historical periods throughout 930-990

WebDewey 2.0 is now available!

WebDewey 2.0 is now available for use. The new WebDewey is easier to use than ever and features:

- An easy-to-navigate, simple user interface that is suitable for the novice as well as the power user
BISAC-to-DDC mappings
- An easy-to-personalize screen display, often done with a single click
- Continuous updating
- No price increase!

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Index Nominum: International Drug Directory 20th Edition ; 01 Mar 2011 : Volume 1: Active Substances and Volume 2: Indexes. ( ISBN: 9783804750531 ); Hardback *** It is accompanied by a CD-ROM ***

For over 50 years, the Index Nominum has been the international standard reference for pharmaceutical substances, trade preparations, synonyms and chemical structures.

Now in its 20th edition, the title has been completely enlarged and revised. It provides an international reference on active substances, their synonyms, chemical structures and formulas, brand names and their manufacturers.

The new edition includes two volumes:

Volume 1: Active Substances and Volume 2: Indexes.

It is accompanied by a CD-ROM with over 16,500 addresses and links to pharmaceutical manufacturers worldwide.

Key Features:

- More than 5,100 active substances (and derivatives) with international non-proprietary names (INN), German, French, Spanish and Latin substance names, structural and molecular formulas, CAS registry numbers and 15,500 synonyms.
- 85,500 proprietary names and more than 16,500 addresses and links to manufacturers from 163 countries
- All single and two-compound preparations and selected three-/four-compound preparations are listed
- Special labelling of paediatric medicines
- Therapeutic groups with ATC codes of the WHO for pharmaceuticals used in human and veterinary medicine
- Valuable search assistance with an alphabetical index of all trade names, pharmaceutical substances and synonyms as well as a separate ATC and ATCvet substance index
- Includes free 60-day online access to Index.

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Index Nominum: International Drug Directory CD-ROM ; [Author:Swiss Pharmaceutical Society]; 21 Mar 2011; (ISBN: 9783804718654 )

For over 50 years, the Index Nominum has been the international standard reference for pharmaceutical substances, trade preparations, synonyms and chemical structures.

Now in its 20th edition, the title has been completely enlarged and revised. It provides an international reference on active substances, their synonyms, chemical structures and formulas, brand names and their manufacturers.
Key Features:
- More than 5,100 active substances (and derivatives) with international non-proprietary names (INN), German, French, Spanish and Latin substance names, structural and molecular formulas, CAS registry numbers and 15,500 synonyms.
- 85,500 proprietary names and more than 16,500 addresses and links to manufacturers from 163 countries
- All single and two-compound preparations and selected three-/four-compound preparations are listed
- Special labelling of paediatric medicines
- Therapeutic groups with ATC codes of the WHO for pharmaceuticals used in human and veterinary medicine
- Valuable search assistance with an alphabetical index of all trade names, pharmaceutical substances and synonyms as well as a separate ATC and ATCvet substance index
- Includes free 60-day online access to Index.

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Dangerous Goods Emergency Action Code List 2011 [Author: National Chemical Emergency Centre (NCEC)]

Author: National Chemical Emergency Centre (NCEC)

The 2011 edition of the Dangerous Goods Emergency Action Code List outlines the Emergency Action codes (EACs), also known as Hazchem codes, for the use of the emergency services in conjunction with Emergency Action Code Cards. EACs indicate to the emergency services actions that may be necessary, during the first few minutes of an incident involving dangerous goods, should the officer in charge of the incident deem it necessary to take immediate actions. It includes details of Hazchem markings on the orange coloured plate of road and rail vehicles, registered in Britain, carrying dangerous goods in bulk or in tanks on domestic journeys.

The Dangerous Goods Emergency Action Code List 2011 is effective from 1 July 2011 and the Emergency Action Code List 2009 should no longer be used from that date.
Key features:
- Section 1: Introduction to the Emergency Action Codes
- Section 2: Displaying Emergency Action Codes
- Section 3: Application of Emergency Action Codes for the Emergency Services
- Section 4: Numerical List of Dangerous Goods, including - United Nations (UN) Number - Substance -Emergency Action Code (EAC) - Advice on Additional Personal Protection (APP) - Hazards - Hazard Identification Number (HIN)
- Section 5: Alphabetical List of Dangerous Goods

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Deutsches Arzneibuch 2010 (DAB 2010) + Europäisches Arzneibuch, 6. Ausgabe Grundwerk 2008 mit Nachträgen 6.1. bis 6.8 + Homöopathisches Arzneibuch 2010 (HAB 2010) + Amtliche deutsche Ausgabe ( ISBN 978-3-7692-5508-9 )

Arzneibuch

Deutsches Arzneibuch 2010 (DAB 2010)
Europäisches Arzneibuch, 6. Ausgabe Grundwerk 2008 mit Nachträgen 6.1. bis 6.8
Homöopathisches Arzneibuch 2010 (HAB 2010)
Amtliche deutsche Ausgabe

2010.
ISBN 978-3-7692-5508-9

Kurztext

Arzneibuch 2010
Das Arzneibuch ist die “Bibel" jedes Pharmazeuten, das Gesetzbuch für die Arzneimittelqualität und -Sicherheit. Was es nicht ist: Es ist kein Verzeichnis aller Fertigarzneimittel (wie die Rote Liste). Das aktuelle Arzneibuch besteht aus:
* Deutschem Arzneibuch 2010 (DAB 2010)
* Europäischem Arzneibuch, 6. Ausgabe 2008, Grundwerk mit Nachtrag 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7 und 6.8
* Homöopathischem Arzneibuch 2010 (HAB 2010)
Diese Werke benötigt jeder selbstständige Apotheker sowie jeder, der Arzneimittel, Ausgangsstoffe, Hilfsstoffe, Reagenzien oder Behältnisse für pharmazeutische Zwecke herstellt oder vertreibt.
Die Ph. Eur. besteht aus einem Allgemeinen Teil mit Analysenmethoden, Behältnissen und deren Materialien, Reagenzien und übergreifenden Monographiegruppen sowie einem Speziellen Teil mit Einzelmonographien.
Das DAB wurde in seiner Struktur der Ph. Eur. angepasst. Nach und nach “wandern" immer mehr Texte aus dem DAB in die Ph. Eur., so dass das DAB schrumpft. Es wird aber sicher immer ein nationales Arzneibuch geben für die Vorschriften, die nicht europaweit gelten.
Auch das HAB ist wie die Ph. Eur. strukturiert. Das HAB wächst kontinuierlich, was auch das zunehmende Interesse an den alternativen Heilmethoden zeigt. Nur Frankreich hat von den Teilnehmerländern der Ph. Eur. ebenfalls ein eigenes Homöopathisches Arzneibuch.
Die Arzneibücher enthalten Analysenvorschriften für Arzneistoffe, Arzneipflanzen, Impfstoffe, Blut und Blutprodukte, Nahtmaterialien, Darreichungsformen, Behältnisse und die dafür verwendeten Materialien, sowie Reagenzien und Hilfsstoffe. Anhand der Vorschriften werden Identität, Reinheit und Gehalt geprüft, also die Qualität von Arzneimitteln sichergestellt. Oberste Priorität hat immer das Europäische Arzneibuch (Ph. Eur.), weil es den freien Warenaustausch zwischen den beteiligten Ländern durch einheitliche Arzneimittelqualität ermöglichen soll.
Mit dem Arzneibuch soll sichergestellt werden, dass
1. für die Arzneimittelherstellung und -aufbewahrung sowohl in der Industrie als auch der Apotheke (Offizin) nur sichere Stoffe höchster Qualität verwendet werden
2. in der Apotheke zur Herstellung von Arzneimitteln oder zur Weitergabe an den Kunden eingegangene Materialien wirklich mit den bestellten identisch sind, in für den Benutzer reiner, also sicherer Form vorliegen und zwar mit einem korrekten Gehalt, also z. B. nicht durch Milchzucker oder gar gefährlichere Substanzen gestreckt
3. ApothekerInnen sichere Arzneimittel in der korrekten Dosierung herstellen können
4. auch in Fertigarzneimitteln verwendete Substanzen identifiziert werden können
5. in Notzeiten der Apotheker die Arzneimittelver- sorgung der Bevölkerung gewährleisten kann.

Deutsches Arzneibuch 2010 (DAB 2010) + Europäisches Arzneibuch, 6. Ausgabe Grundwerk 2008 inkl. Nachträge 6.1. - 6.8, Amtliche deutsche Ausgabe ( German Pharmacopoeia - Farmacopéia Alemã ) \ ( ISBN 978-3-7692-5399-3 )

Arzneibuch
Deutsches Arzneibuch 2010 (DAB 2010)
Europäisches Arzneibuch, 6. Ausgabe Grundwerk 2008 inkl. Nachträge 6.1. - 6.8, Amtliche deutsche Ausgabe

2010.
ISBN 978-3-7692-5399-3

Kurztext

Das Europäische Arzneibuch besteht aus einem Allgemeinen Teil mit Analysenmethoden, Behältnissen und deren Materialien, Reagenzien und übergreifenden Monographiegruppen sowie einem Speziellen Teil mit Einzelmonographien.

Das Deutsche Arzneibuch wurde in seiner Struktur der Ph. Eur. angepasst. Nach und nach “wandern" immer mehr Texte aus dem DAB in die Ph. Eur., so dass das DAB schrumpft. Es wird aber sicher immer ein nationales Arzneibuch geben für die Vorschriften, die nicht europaweit gelten.

Die Arzneibücher enthalten Analysenvorschriften für Arzneistoffe, Arzneipflanzen, Impfstoffe, Blut und Blutprodukte, Nahtmaterialien, Darreichungsformen, Behältnisse und die dafür verwendeten Materialien, sowie Reagenzien und Hilfsstoffe. Anhand der Vorschriften werden Identität, Reinheit und Gehalt geprüft, also die Qualität von Arzneimitteln sichergestellt. Oberste Priorität hat immer das Europäische Arzneibuch (Ph. Eur.), weil es den freien Warenaustausch zwischen den beteiligten Ländern durch einheitliche Arzneimittelqualität ermöglichen soll.

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European Pharmacopoeia 7th Edition - Book subscription 2012 (Volumes 7.0 ; 7.01 ; 7.02 . 7.03 ; 7.04 ; 7.5) \ (ISBN: 978-92-871-6706-4 + 978-92-871-6962-4) ; Book or USB Stick or Online or Packages - English - French - Spanish - Bilingual

NEW: For the 7th Edition, the EDQM will be changing its electronic version from DVD-ROM to USB stick. The development will feature a new "portability" option allowing users to run the European Pharmacopoeia application directly from the USB drive following a one-time licensing procedure and with no further installation (provided .NET 2.0 is installed on the target computer). This will therefore be of direct benefit for users who have more than one computer or need to access from other computers while travelling. In addition, the USB stick will continue to allow two fixed installs as is currently the case with the DVD-ROM.

7th EDITION EUROPEAN PHARMACOPOEIA
- 7th Edition Book
- 7th Edition USB Stick
- 7th Edition Online

- 7th Edition Packages

About the European Pharmacopoeia

The texts of the European Pharmacopoeia (Ph. Eur.) concern the qualitative and quantitative composition of medicines, the tests to be carried out on medicines, on the raw materials used in the production of medicines and on the intermediates of synthesis. It contains texts covering substances, excipients and preparations for pharmaceutical use of chemical, animal, human or herbal origin, homoeopathic preparations and homoeopathic stocks, antibiotics, as well as dosage forms and containers. The texts also cover biologicals, blood and plasma derivatives, vaccines and radiopharmaceutical preparations. They are legally binding.

Versions and SubscriptionsThe Ph. Eur. is supplied in a variety of formats designed to be flexible to suit the needs of your organisation. It is available in 3 formats - print, online and USB stick. Book Version: The subscription to the two initial volumes (Vol. 1 and 2) and two supplements (Supplement 7.1 and 7.2) is now available to order. Plus access to the archives is also possible. Online Version: The online subscriptions provide access to all updates posted and to the archives starting from 1969 (1st Edition). Subscribers have access up to Supplement 7.2 from July 2010 until 31 December 2011. NEW! USB Version: The new USB stick version makes it easy to access the Ph. Eur. while on the move or in environments where the use of the print or online versions would be inappropriate or impractical. It is also ideal for users who have more than one computer. Access to the archives is also possible. NEW! Packages: Three different packages are now available if interested in having more than one version. The Ph. Eur. is available in the English and French. Its translation into Spanish is underway and the texts are accessible on the online version as they become available. Place an Order If you need more information on product prices, if you wish to see the products' lists of contents, or if you want to order and or to pay, please contact us. DESCRIPTION

This subscription contains: - the base volume 7.0 (published in July 2010 - for implementation January 2011). - supplement 7.1 (published in October 2010 - new/revised texts agreed in March 2010 - for implementation in April 2011), and - supplement 7.2 (published in January 2011 - new/revised texts agreed in June 2010 - for implementation in July 2011). - supplement 7.3 (published in June 2011 - new/revised texts agreed in November 2011 - for implementation in January 2012), - supplement 7.4 (published in October 2011 - new/revised texts agreed in March 2011 - for implementation in April 2012), and - supplement 7.5 (published in January 2012- new/revised texts agreed in June 2011- for implementation in July 2012). Click to enlarge picture

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USP 35-NF 30 - Publication Date : 30 Nov 1, 2011 - Official Date : May 1, 2012 + 1st Supplement to USP 35–NF 30 - Publication Date February 2012 - Official Date : August 1, 2012 + 2nd Supplement to USP 35–NF 30 - Publication Date: June 2012 - Official Date : December 1, 2012 ( in English and Spanish now available )

United States Pharmacopeia–National Formulary (USP–NF)The USP-NF is a combination of two official compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. USP-NF standards are enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States.

Published annually in an official English edition (print, CD, online) and an official Spanish edition (print).

USP 35-NF - Publication Date : 30 Nov 1, 2011 - Official Date : May 1, 2012
- 1st Supplement to USP 35–NF 30 - Publication Date February 2012 - Official Date : August 1, 2012
- 2nd Supplement to USP 35–NF 30 - Publication Date: June 2012 - Official Date : December 1, 2012

Para maiores informações:

Por favor, entre em contato:

Email: jhecker@uol.com.br
Linkedin: heckerjf
Twitter: @heckerjf
Facebook: PubIntl

British Pharmacopoeia 2012 ; [British Pharmacopoeia Commission]; (ISBN: 9780113228690) - bp2012

The British Pharmacopoeia (BP) 2012 is the leading collection of standards for UK medicinal products and pharmaceutical substances. Produced by the British Pharmacopoeia Commission Secretariat of the Medicines and Healthcare products Regulatory Agency, the BP makes an important contribution to public health by setting publicly available standards for the quality of medicines.

Now used in over 100 countries, the BP remains an essential reference for all individuals and organisations working within pharmaceutical research and development, manufacture and testing across the globe.

The print edition of the BP 2012 comprises five volumes of the British Pharmacopoeia 2012 and a single volume of the British Pharmacopoeia (Veterinary) 2012.

The British Pharmacopoeia 2012 package includes:
- Six volume printed edition
- Single-user licence to the CD-ROM
- Single-user licence to the online version

The BP 2012 online includes free in-year updates to harmonise with the European Pharmacopoeia. These updates will be published online as follows:
- January 2012
-  April 2012
- July 2012

Clearly laid out sections include monographs which set out the mandatory standards for active substances, excipients, formulated preparations, blood-related products, immunological products, radiopharmaceutical preparations, surgical materials, herbal and complementary medicines, together with supporting General Notices, test methods, infrared spectra and supplementary information.

European Pharmacopoeia monographs are clearly distinguished and cross-referenced, while a full index ensures easy access to the current legally binding UK standards.

Online access/CD-ROM
You will receive an ID code for the BP 2012 online with your printed copy. Once you have registered using this code you will be granted a single-user licence to access the BP online. You also have the option to receive the CD-ROM which contains the full content of the BP 2012.

Access the BP across your organisation
For organisations with several employees that need simultaneous access to the vital content contained in the BP 2012, a concurrent licence is the most efficient solution. Networking information throughout your organisation in this way provides maximum access through any workstation, with considerable savings over purchasing multiple subscriptions.

Key Features:

-  Legally effective in the UK from 1 January 2012
- A six volume printed set, including a single volume of the BP (Veterinary) 2012, together with a fully searchable CD-ROM and online access to provide you with a flexible resource
- 35 new BP monographs for formulated preparations
- Additional standards for widely used unlicensed medicines
- European Pharmacopoeia 7th edition material up to and including Supplement 7.2
- Three free in-year updates for the BP online to harmonise with the European Pharmacopoeia.

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Bosch Automotive Handbook, 8th Edition ; 2011; [Robert Bosch]; (ISBN: 978-0-7680-4851-3)

This latest edition of the best-selling, indispensable reference book has been completely updated with more than 580 pages of new content, including new or greatly revised sections on:

Internal-combustion engines: gasoline and diesel
Spark-ignition engine management: fuel supply, LPG operation
Diesel-engine management: common-rail injection system
Turbochargers and superchargers
Hybrid drives
Fuel cells for the vehicle drive
Chassis systems: suspension, shock absorbers, steering
Chassis control and active safety: driving-dynamics control system
Automotive electrics: vehicle electrical systems, electrical machines
Automotive electronics: automotive software engineering, networking, buses

Detailed enough to address complex technical issues yet portable enough to take everywhere, the 8th edition Handbook also contains more than 1,000 illustrations, diagrams, tables, and sectional drawings.

Published By: Robert Bosch
Published: June 2011
Pages: 1266
Binding: Softbound
Product Code: BOSCH8
Product Status: Available

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Ordering Reproductions of John James Audubon’s Birds of America ( all 435 paintings in John James Audubon's masterwork ) 2011

The University of Pittsburgh is fortunate to own one of the rare, complete sets of John James Audubon’s Birds of America. It is considered to be the single most valuable set of volumes in the collections of the University Library System (ULS). Indeed, only 120 complete sets are known to exist.

While Audubon was creating Birds of America, he was also working on a companion publication, namely, his Ornithological Biography. Both of these sets were acquired by William M. Darlington in the mid-nineteenth century and later donated, as part of his extensive library, to the University of Pittsburgh. Recognizing that the Darlington Library includes significant historical materials, such as rare books, maps, atlases, illustrations, and manuscripts, the ULS charted an ambitious course to digitize a large portion of Mr. Darlington’s collection, including the Birds of America.

The University of Pittsburgh Library System is pleased to provide print reproductions from its double elephant folio edition of the Birds of America.

The reproductions are based on high-resolution digital images of the original work of art scanned by the University’s Digital Research Library on an A0 DigiBook SupraScanner. Each plate was digitized at a resolution of 400 ppi true color (24-bit) using a 14000 pixel CCD linear array camera.

We offer four different reprint sizes all produced from the digital source using the giclée process (i.e., ink-jet printing). The Full size is reproduced at 100% of the plate’s original size (26 x 38 inches), including a one-inch border extending beyond the actual plate. Please see the various sizes and pricing on the reverse.

The plate reproductions are printed on 285 gram smooth fine art paper for digital reproductions. The paper is made of 100% cotton linters and traditional matte finish designed for long-term fade-resistant reproductions. The mould-made fine art paper is free of acid and lignin, thus exhibiting high archival quality. Please note that these reproductions are not scuff-proof and should be treated as fine art.

The ULS has contracted with Warren Associates of Pittsburgh to print the plates. They will be shipped in heavy weight mailing tubes via commercial carrier. From receipt of payment to delivery, orders will take approximately four to six weeks to process.

The price of each reproduction includes shipping and handling (within the continental U.S.). The ULS can only accept a check or money order made payable to the University of Pittsburgh. You will be contacted by email to verify your order prior to printing.

Paper Sizes Available:
- Full (original) 27 ¾ x 40 ¼ inches
- Large 20 ¾ x 30 inches
- Medium 12 ¾ x 19 inches
- Small 9 ¾ x 14 inches $ 50.00 (original) 27 ¾ x 40 ¼ inches

Originally sold on subscription basis between 1827-38, the work was priced at $1,000 and was unbound. Its value today is about $9 million, said Dabrishus, who added that the Carnegie Museum of Natural History also owns a folio.



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Manual for Railway Engineering 2011 (4 Volume Set - Volume 1 Track - Volume 2 Structures - Volume 3 Infrastructure and Passenger - Volume 4 Systems Management - in Loose-Leaf Format, in Case / CD-ROM (Single User - Multi-User License fees) - Combination Set - Annual Publication released every April - AREMA publishes standards and best practices for railway engineering

The Manual for Railway Engineering (MRE) is an annual publication released every April. The Manual consists of more than 4000 pages of railway engineering reference material, the recommended practices for the industry. It contains principles, data, specifications, plans and economics pertaining to the engineering, design and construction of the fixed plant of railways (except signals and communications), and allied services and facilities. The material is developed by AREMA technical committees and is published as a guide to railways in establishing their individual policies and practices relative to the subjects, activities and facilities covered in the Manual, with the aim of assisting them to engineer and construct a railway plant which will have inherent qualities of safe and economical operation as well as low maintenance cost. Chapters are grouped into four general categories, each in a separate volume: Track * Structures * Infrastructure and Passenger * Systems Management.

- Ch. 1 - Roadway & Ballast
- Ch. 4 - Rail
- Ch. 5 - Track
- Ch. 30 - Ties

- Ch. 7 - Timber Structures
- Ch. 8 - Concrete Structures & Foundations
- Ch. 9 - Seismic Design for Railway Structures
- Ch. 15 - Steel Structures

- Commuter, Transit & High Speed Rail
- Ch. 6 - Buildings & Support Facilities
- Ch. 11 - Commuter and Intercity Rail Systems
- Ch. 12 - Rail Transit
- Ch. 14 - Yards and Terminals
- Ch. 17 - High Speed Rail Systems
- Ch. 18 - Light Density and Short Line Railways
- Ch. 27 - Maintenance-of-Way Work Equipment
- Ch. 33 - Electrical Energy Utilization

- Ch. 2 - Track Measuring Systems
- Ch. 13 - Environmental
- Ch. 16 - Economics of Railway Engineering and Operations
- Ch. 28 - Clearances
- AAR Scale Handbook

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