2017 / 2018 - Deutscher Apotheker Verlag · The British Pharmacopoeia 2018 supersedes the BP 2017....

InternationalPharmaceutical and Medical

Publications

2020

All prices include VAT in Germany unless otherwise specified. Prices may be subject to change without notice. www.deutscher-apotheker-verlag.de2

Pharmacopoeia

The single reference work for the quality control of medicines and substances for pharmaceutical use in Europe

The official standards provide a scientific basis for quality control during the entire life cycle of a product. The European Pharmacopoeia (Ph. Eur.) is Europe’s legal and scientific benchmark for pharmaco-poeial standards which contribute to delivering high quality medicines in Europe and beyond. The Ph. Eur. is applicable in 39 European countries and applied in more than 120 countries worldwide. The 10th Edition (initial release plus supplements 10.1 and 10.2) contains 2,426 monographs, 372 general texts (including general monographs and methods of analysis) and around 2,780 descriptions of reagents. The 10th Edition consists of 3 initial volumes (Main volume 10.0) complemented by 8 updates issued three times a year to create collection of 8 supplements (10.1 to 10.8) until 2022. In addition, the European Pharmacopoeia Archives are available to all users with an up-to-date subscription (print or electronic) until the end of each valid year.

Electronic version: • Improved visibility of changes (for revised and corrected texts)• Completely cumulative versions, bilingual (English and French), with new features and direct

access to complementary information (Knowledge Database).• Access to the website from all recent common operating systems (tablet and smartphone).• Application fully compatible with recent Windows and Linux operating systems.

European Pharmacopoeia 10th Edition Published under the direction of the European Directorate for the Quality of Medicines and HealthCare (EDQM)

Book: Hardcover. On continuation. Available in English or French.

Subscription to the 10th Edition first year – valid year 2020: Contains main work (3 initial volumes 10.0), plus non-cumu-lative supplements 10.1 and 10.2. Incl. online archive.English language. € 577,80 ISBN 978-3-7692-7453-0

French language. € 577,80 ISBN 978-3-7692-7454-7

Subscription to the second year – valid year 2021: Non-cumula-tive supplements 10.3-10.5. Incl. online archive.English language. € 577,80 ISBN 978-3-7692-7606-0

French language. € 577,80 ISBN 978-3-7692-7634-3

Special price for Packages electronic version + book:

Access to 10.0–10.2 – valid year 2020: 1 electronic version licence, bilingual. 1 named user + Book Subscription to 10th Edition first year (10.0–10.2): € 930,00 (instead of € 1.155,60)

Book in English language: ISBN 978-3-7692-7455-4

Book in French language: ISBN 978-3-7692-7456-1

Access to 10.3–10.5 – valid year 2021: 1 electronic version licence, bilingual. 1 named user + Book Subscription to 10th Edition second year (10.3–10.5): € 930,00 (instead of € 1.155,60)

Book in English language: ISBN 978-3-7692-7639-8

Book in French language: ISBN 978-3-7692-7640-4

Electronic version: One licence, bilingual: English and French. Access for 1 named user. Price per licence.

Access to 10.0–10.2 – valid year 2020: Content of main work 10.0 and first 2 cumulative updates. Incl. online archive. € 540,– + VAT

Access to 10.3–10.5 – valid year 2021: 3 cumulative updates. Incl. online archive. € 540,– + VAT

European Pharmacopoeia 10th Edition

NewSupplements

How can one European Pharmacopoeia electronic version licence be used?

ELECTRONIC VERSION LICENCE 2 options: one to be chosen

INDIVIDUAL ACCESS 3 possibilities

SHARED ACCESS Download the application

2 options: one to be chosen

Access from one Windows session on that computer

(e.g. same user name and password)

ONLINE via web

browser and user

credentials

Download the application and corresponding pack

2 possibilities

• Online access: when connected to internet

• Offline access: when not connected to internet

and

or

• Install the application to all Windows sessions (admin rights required)

• Shortcut Ph. Eur. on desktop, activation code needed (to be saved and accessible to all users)

• Install the application • Shortcut Ph. Eur. on

desktop

Stick borrowed by different users

ON ONE COMPUTER

ON ONE COMPUTER

or

or

or

and and

ON ONE USB

Access from any Windows session on that computer

(e.g. different usernames and passwords) limited to one user

simultaneously

or

or

or

ON ONE USB

Multiuser

prices on demand.

Please ask

for an offer.

www.edqm.eu

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Publication Schedule 10th Edition

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Errors excepted. Free shipping within Germany, delivery abroad plus € 7,95 shipping per parcel. 3

Pharmacopoeia

www.deutscher-apotheker-verlag.de

USP-NF Online: Rolling subscription. 365 days access via Access Point. Continually updated. Price for 1 named user: € 739,00 + VAT TN 176106100

Web browser: Microsoft® Internet Explorer 11 or Google© Chrome Pentium II processor, 350 MHz or faster, 128 MB RAM SVGA video or better, Monitor with 1024 x 768 resolution

Please ask for an offer for multiuser access.

USP–NF: U.S. Pharmacopeia & National Formulary A publication of the United States Pharmacopeial Convention

USP-NF Mobile App (Apple/Android)Rolling subscription. 365 days access. Continually updated. Price for 1 subscription (installation and data sync on up to two (2) mobile devices: € 739,00 + VAT TN 176107100

OS: iOS 12 and up or Android 6.0 and upPhone: iPhone 7, iPhone 8, iPhone X or Samsung Galaxy, Google PixelTablet: iPad 9.7'' and up or Samsung 10'' and up

USP-NF United States Pharmacopeia (USP) and National Formulary (NF)

The United States Pharmacopeia and National Formulary (USP–NF) is a combination of two official compendia. 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 US. Food and Drug Administration for medicines manufactured and marketed in the United States.

A monograph includes the name of the ingredient or preparation; the definition; packaging, storage and labeling requirements; and the specification. The specification consists of a series of tests, procedures for the tests, and acceptance criteria. Medicinal ingredients and products will have the stipulated strength, quality, and purity if they conform to the requirements of the monograph and relevant general chapters.

The USP-NF Online subscriptions are available for one year for one or more users. The subscriptions include access to all updates posted online during the 12 months after the subscription start date. Each new update that is posted integrates content from all previous editions to date. Online access includes extensive search capabilities; a glossary of frequently asked questions; and quick search, bookmarking, printing, and copy/paste functions. It also includes "My USP-NF", a special online tool that let's you save frequent searches, bookmark important pages, and create a custom table of contents. Also featuring pronunciations.

The USP-NF Mobile App allows you to access USP-NF content no matter where you are, even if you don't currently have internet access. While the layout and functionality of the USP-NF Mobile App is somewhat different from the full-featured USP-NF Online platform, rest assured that you still have access to all of the current content in the USP-NF Online. The App notifies you to synchronize with the USP-NF Online at the end of each month to ensure that you have access to the latest updates to USP-NF documents, as soon as they are published. Please note: Only "Currently Official" (green) and "Not Yet Official" (yellow) USP-NF content is accessible on the USP-NF Mobile App. The application automatically removes versions that are "No Longer Official" at the end of each month. This allows for more rapid downloads and synchronization of content.

One subscription allows installation and data sync on up to two (2) mobile devices, and does not require Access Point account registration.

USP-NF Archive USB-StickA publication of the United States Pharmacopeial Convention

USP 28-NF 23 through USP 36-NF 31: 2015. USB-Stick. Single user. Updates to be charged. € 1.576,– + VAT ISBN 978-3-7692-6526-2

USP 37-NF 32 Archive: 2015. USB-Stick. Single user. € 221,– + VATISBN 978-3-7692-6635-1





Gain convenient access to previously official USP-NF contentThis valuable reference tool designed for scientists and industry professio-nals is available electronically.Housed on single USB flash drives, the extensive PDF archive includes previously official editions of USP-NF.

Work smarter with a tool that helps:• Save time researching revisions

to monographs and general chapters

• Easily review original compendial data

• Compare and track documen-tation over time

• Save shelf space!

Users now have convenient access to an extensive set of documented standards that can be easily browsed, searched, and printed.

New

New

All prices include VAT in Germany unless otherwise specified. Prices may be subject to change without notice. www.deutscher-apotheker-verlag.de4

British Pharmacopoeia 2020

New for the BP 2020:• 35 new BP monographs• 40 new Ph. Eur. monographs • 331 amended BP monographs • Five new monographs for unlicensed

formulations• Two new monographs for herbal

medicines• One new and one amended BP

Veterinary monographs• All monographs from the European

Pharmacopoeia 9th Edition including Supplements 9.1 to 9.8

• Three in-year online and offline download product updates to integrate the European Pharma- copoeia Supplements 10.0 to 10.2

Multiuser access: • If you want access for more than one

user you need a multiuser access.• The online format is easy to network,

allowing access for a specified number of concurrent users on one site or global access for multisites.

• Instant online access via IP recognition

Please ask for an offer for multiuser access.

Pharmacopoeia

British Pharmacopoeia 2020 + British Pharmacopoeia (Veterinary)

Book: 2019. Approx. 6,700 pages. Slipcase containing 6 volume books + Download (single user*)+ Online access (single user*). € 1.478,– ISBN 978-3-7692-7467-7

New, legally enforced standards, effective on 1 January 2020. All European Pharmacopoeial texts included.

The British Pharmacopoeia 2020 supersedes the BP 2019 and becomes legally effective on 1 January 2020. This edition incorporates new monographs from both the BP and European Pharmacopoeia along with a significant number of revised monographs.

Updated annually, the BP is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products.

The BP 2020 includes approx. 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or activepharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP, making it a convenient and fully comprehensive set of standards that can be used across Europe and beyond.

The British Pharmacopoeia 2020 package consists of• A six-volume printed edition, including the BP (Veterinary) 2020• A single-user online licence* for BP Online• A single-user download for offline use* * These single-user licences are granted solely to the designated holder of the product within an organisation.

Edited by the British Pharmacopoeia Commission

A publication of The Stationery Office

Errors excepted. Free shipping within Germany, delivery abroad plus € 7,95 shipping per parcel. www.deutscher-apotheker-verlag.de 5

German Homoeopathic Pharmacopoeia

Pharmacopoeia

Pharmacopoeia of the People’s Republic of China Edited by the Chinese Pharmacopoeia Commission

10th edition 2017. English version. 4 hardback volumes with slipcases. Hardcover. € 1.170,– TN 118483003

This 2015 edition provides the statutory requirements for foreign pharmaceutical companies producing medicines for the Chinese market. It came into effect on 1st December 2015.

The Pharmacopoeia of the People's Republic of China 2015 covers both traditional Chinese medicines and western medicines. It gives descriptions and information on the standards of purity, testing, dosage, precautions, storage, and the strength of each drug.

The Chinese Pharmacopoeia 2015 edition comprises Volumes I, II, III and IV and contains a total of 5608 types of medicinal product, including 1,082 new revisions.

Volume IV is new to this edition. Various appendices of the previous edition of the pharmacopoeia have been consolidated into the Volume IV of this edition of the pharmacopoeia.

Published in four volumes:

Volume I - contains a total of 2,598 types of medicinal materials and the prepared slices of Chinese crude drugs, vegetable, oil fat and extracts and single-item preparations

Volume II - contains a total of 2,603 types of chemical drugs, antibiotics, biochemical drugs and radioactive drugs

Volume III - contains a total of 137 biological products

Volume IV - contains a total of 317 general requirements

This title supersedes the 2010 edition of the Chinese Pharmacopoeia.

Pharmacopoeia of the People's Republic of China

German Homoeopathic Pharmacopoeia (GHP)Translation of the German Homöopathisches Arzneibuch Amtliche Ausgabe (HAB)Translated from German by Dr. Stephen Benyunes, RWS Group – Medical Translation Division, Bucks

New supplements

Newonline

Print: Complete work including 16th Supplement 2019 2,366 pages. 2 ringbinders. Loose-leaf serial. € 380,– ISBN 978-3-8047-5084-5

Online: Rolling subscription. 365 days access. Continually updated. Price for 1 concurrent user, first year: € 345,– + VATTN 271801100

Free 24-hours-trial on demand! The German Homoeopathic Pharmacopoeia (GHP) is one of the most important homoeopathic pharmacopoeiae worldwide.

The official German-language Homöopathisches Arzneibuch (HAB) has been translated into the English language, making this widely acclaimed work available to the global community of• Homoeopathic manufacturers• Homoeopathic physicians• Non-medical practitioners• Pharmacists and• National registration authorities.

Professionals engaged in all aspects of the manufacture, evaluation, registration or dispensing of homoeopathic substances or medicinal products now have access to a wealth of information comprising about 600 monographs and general texts including reagents, vehicles and excipients analytical and the very important manufacturing methods. Homoeopathic and anthroposophical manufacturing methods are included as well as the methods used in spagyrics and the production of organ-derived preparations. The analytical methods have been harmo-nized with the European Pharmacopoeia (Ph. Eur.) and the German Pharmacopoeia (DAB).

Each monograph is uniformly structured, listing • origin • description • characteristics • identification • purity tests• assays

and providing information on the basic dosage forms and their* manufacture* characteristics* identification* purity tests* assays and* storage.

The GHP Online edition allows a convenient online search encompassing the entire database and is given a cumulative update each year.

All prices include VAT in Germany unless otherwise specified. Prices may be subject to change without notice. www.deutscher-apotheker-verlag.de

Reference Books

AHFS DI on MedicinesComplete Online

Yearly subscrip tion fee, 365 days Online access . Base prices:

For 1 concurrent user, one site – Healthcare € 1.948,– + VAT For 1 concurrent user, one site – Companies € 2.435,– + VAT

Quote and a free 10-days-trial on demand.

AHFS DI Online at www.DrugBase.de

Continually updated. Yearly licence fee for one-concurrent user from one location:

For Individuals or Community / Retail Pharmacy: € 434,– + VAT

For Hospitals or Hospital Pharmacies: € 868,– + VAT

For Companies or Institutions: € 1.736,– + VAT

Other prices apply for additional locations or additional concurrent users. Pharmacy Chains – Please ask for quotation.

Free 10-days-trial at www.DrugBase.de!

Your Bonus: As part of the database portal www.DrugBase.de, every search will return hits from all of the other databases integrated in the portal.

Further databases in English language at www.DrugBase.de: • Fiedler Encyclopedia

of Excipients • Handbook on Injectable

Drugs• Index Nominum • Medicinal Plants

AHFS Drug Information® 2020

New

AHFS Drug Information 2020American Hospital Formulary Service Drug InformationA publication of the ASHP American Society of Health-System Pharmacists

2020. 3,840 pages. Softcover. € 496,–ISBN 978-3-7692-7547-6

New

AHFS is the only drug information resource curated by a not-for-profit scientific organization and the only remaining original federal compendium whose authority for establishing accepted medical uses includes the broadest scope of drugs and indications under Medicaid, Medicare Part D, and more.

Trusted by pharmacists and other healthcare professionals for over 60 years, AHFS® DI™ is the most comprehensive evidence-based source of drug information complete with therapeutic guidelines and off-label uses.

With expanded and revised content supported by more than 94,000 references and incorporating the advice of numerous subject matter experts, AHFS® DI™ helps you protect your patients. Each edition includes additional online monographs, which are updated throughout the year, and can be found on the For Subscribers section of ahfsdruginformation.com. The password can be found in the preface of the printed edition.

Updates for this edition include:

Special Feature: A discussion of recent evidence questioning aspirin’s role in primary prevention of cardiovascular events in most adults, including the American College of Cardiology and American Heart Association’s positions.

• Management of opiate use disorder • Multimodal pain management strategies for

non-opiate analgesic agents and opiate-sparing drugs

• Current best practices for management of pain and sedation in critically ill patients such as the concept of analgosedation and comparisons of various sedative agents used for ICU sedation

• Newly published information on breakthrough oncology drugs approved as part of the FDA’s accelerated approval program

• Updating of pharmacogenomic considerations related to dosage adjustments (e.g., tamoxifen) or risk of sensitivity reactions (e.g., allopurinol, phenytoin or fosphenytoin)

• Expanded information on non-oncology off- label uses (e.g., mycophenolate in treating scleroderma; ketamine use in treatment- resistant depression)

• Addition of new therapies for the treatment of seizure disorders, including status epilepticus and intractable childhood epilepsy syndromes

• Use of Calcitonin Gene-Related Peptide (CGRP) antagonists in the preventive treatment of migraines

• Important changes in management of diabetes, including effects of SGLT2 inhibitors and GLP-1 agonists on cardiovascular risk reduction and beneficial effects on renal function

Errors excepted. Free shipping within Germany, delivery abroad plus € 7,95 shipping per parcel. www.deutscher-apotheker-verlag.de

Reference Books

7

Martindale The Complete Drug Reference

Martindale + ADR on MedicinesComplete OnlineYearly subscrip tion fee - 365 days Online access. Base prices:

For 1 concurrent user, one site – Healthcare € 2.753,– + VAT

For 1 concurrent user, one site – Companies € 3.223,– + VAT

MedicinesComplete provides online access to some of the world‘s leading drug and healthcare references.

Further databases:• AHFS DI• British National Formulary• BNF for Children• Clarke‘s Analysis of Drugs and

Poisons • Dale & Appelbe's Pharmacy and

Medicines Law• Dietary Supplements• Drug Administration via

Enteral Feeding Tubes• Drugs in Pregnancy and

Lactation • Handbook on Injectable

Drugs• Herbal Medicines • Injectable Drugs Guide• Kucers’ the Use of Antibiotics• Pediatric Injectable Drugs• Pharmaceutical Excipients• Stockley‘s Drug Interactions • Stockley’s Herbal

Medicines Interactions• The Green Guide • The Orange Guide

The integrated search enables you to search across many thousands of drug, poison, excipient, interaction and herbal mono-graphs and brings together a wealth of clinically relevant, unbiased information at your fingertips.

Integrated Healthcare Information for Professionals

Quote and a free 10-days-trial are available on demand.

New

Martindale: The Complete Drug Reference is depended upon by healthcare professionals throughout the world for its reliable and comprehensive information on international drugs and medicines. It is widely recognised for its unbiased and authoritative nature, as well as its unprecedented international coverage, including information from 43 countries and regions.

A team of experts use the most clinically relevant and reliable information, giving healthcare professionals a complete resource for reference on drugs and medicines.

Martindale contains proprietary drug information on preparations available worldwide, and remains a critical tool for identification of the local equivalent of a prescribed preparation and for assessing what alternatives might be suitable when needed.

Unique benefits:• Breadth: No other source has the breadth of coverage or level of detail making it the ideal

first-line reference work as well as a trusted source of information for more detailed drug enquiries

• Global coverage: Martindale is the leading resource in terms of internaional coverage, with 43 countries covered – alternative publications have a narrow regional focus

• Objectivity: Respected for its accuracy of content and independence from pharmaceutical industry. Based on published information and extensively referenced

• International adoption: Recognised and adopted worldwide

New

Martindale The Complete Drug Reference Edited by Robert Buckingham, Royal Pharmaceutical Society, London. A publication of the Pharmaceutical Press

40th revised and updated edition 2020. 2 volumes in slipcase. 4,912 pages. Hardcover. € 674,–Prepublication price valid until 31 October 2020: € 598,–TN 180046064


Valid for 365 days via Username/Password

8

Handbook on Injectable Drugs on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices:For 1 concurrent user, one site – Healthcare € 1.256,– + VAT For 1 concurrent user, one site – Companies € 1.908,– + VAT


Handbook on Injectable Drugs

Other prices apply for additional locations or additional concurrent users. Pharmacy Chains – Please ask for quotation.

Free 10-days-trial at www.DrugBase.de!

Your Bonus: As part of the database portal www.DrugBase.de, every search will return hits from all of the other databases integrated in the portal.

Further databases in English language at www.DrugBase.de:• AHFS DI • Fiedler Encyclopedia

of Excipients• Index Nominum • Medicinal Plants

Handbook on Injectable Drugs at www.DrugBase.de

Continually updated. Yearly licence fee for one-concurrent user from one location.

For Individuals or Community / Retail Pharmacy: € 417,– + VAT

For Hospitals or Hospital Pharmacies: € 834,– + VAT

For Companies or Insti- tutions: € 1.668,– + VAT

Reference Books

Handbook on Injectable DrugsA publication of the American Society of Health-System Pharmacists

20th updated edition 2018. 1,400 pages. Hardcover. € 445,–ISBN 978-3-7692-7332-8

ASHP’s Guide to IV Compatibility and StabilityBacked by quality, peer-reviewed published literature, the Handbook on Injectable Drugs® has been a go-to, trusted resource for more than four decades. Authored under the editorial authority of AHFS Drug Information® and published by ASHP, it's the global gold standard for IV compatibility and stability information.

• Provides newly updated information, and features

• 27 new monographs, 23,663 compatibility pairs, and 276 new references.

• With its 40-year track record of precise, accurate detail, nothing else comes close for compatibility, stability, storage, and preparation of parenteral drugs.

A compilation of the United States Adopted Names (USAN), current USP and NF names for drugs, and other nonproprietary drug names

A publication of USP United States Pharmacopeial Convention

USP USAN Online: Exclusively online: Rolling subscription, valid for 365 days from date of activation. Updated and revised annually each January. Price per ID: € 387,00 plus VAT

USP Dictionary of USAN and International Drug Names

The most comprehensive, official source of established drug names and other essential drug information. This is your fast, easy reference for accurate compliant work.

The USP Dictionary of USAN and International Drug Names is the leading reference for nonproprietary drug names and chemical structures. In addition to USANs, the USP Dictionary provides Interntional Nonproprietary Names (INNs), British Approved Names, Japanese Accepted Names, brand names, Unique Ingredient Identifier (UNII) codes, manufacturers, official USP-NF names, moleculare weights, graphic formulas, pharma-cologic and/or therapeutic categories and pronunciations.

The 2020 edition features the latest drug name updates and information, including:• 6,226 United States Adopted Names (USAN) - 203 are new• 12,872 nonproprietary drug name entries• 3,547 brand names• 15,224 Unique Ingredient Identifier (UNII) codes• 7,423 code designations, including 402 Cancer Chemotherapy

National Service Center (NSC) numbers• 14,839 Chemical Abstract Service (CAS) registry numbers• 10,700 graphics• 203 new pronunciations

The USP Dictionary helps to:• ensure official compliance in product labeling in order to

obtain new drug approval and to avoid "misbranded" producs

• determine established generic drug names to use in advertising and labeling as required by U.S. federal law

• preserve trademark rights to drug brand names by using proper generic names

• file accurate and acceptable INDs, NDAs and ANDAs• avoid errors in reports, correspondence, articles and package

inserts• verify names and spellings of materials used in laboratory

research• group drug products into families• determine exact chemical structures and compositions• avoid serious verbal medication errors

USP Dictionary will be available exclusively in online format and will be updated and revised annually each January. Subscription will be a rolling subscription, valid for 365 days from date of activation.

New

Errors excepted. Free shipping within Germany, delivery abroad plus € 7,95 shipping per parcel. www.deutscher-apotheker-verlag.de

Handbook ofPharmaceutical Excipients

Edited by Paul J. Sheskey, Walter G. Cook, Colin G. CableA publication of the Pharmaceutical Press

8th revised and updated edition 2017. 2 volumes in slipcase. 1,216 pages. Hardcover. € 487,– TN 180046051

The Handbook of Pharmaceutical Excipients collects together essential data on the physical properties of excipients as well as providing information on their safe use and applications. All of the 400+ monographs are also thoroughly cross-referenced and indexed to allow their identification by chemical, non-proprietary or trade names. It is internationally recognised as the authoritative source of information on pharmaceutical excipients and a compre-hensive guide to uses, properties and safety.

Changes to this new edition:• Contains revised and updated monographs• 20+ new monographs including amino acids Arginine, Proline

and Asparagine• Includes newly added Raman spectra for many excipients• New chapter content including information on excipients in oral

solid dose formulations, and pediatric formulations

New Formulation Considerations and Related Information chapters on:• Functional Categories of Pharmaceutical Excipients• Pharmaceutical Excipients in Pediatric Formulations• The Selection of Excipients for Oral Solid Dosage Forms• Reactive Components in Pharmaceutical Excipients

Over 400 Monographs benefiting from a standardized, easy-to-use template including:• pharmacopoeial information from the UK,

Europe, Japan and the United States• non-proprietary names and synonyms• chemical name and structure,

CAS Registry number, empirical formula, molecular weight

• functional category, applications and incompatibilities

• material description and typical excipient properties

• safety, stability, storage and handling information

• method of drug manufacture• related substances• primary references• editorial comments• author details and revision date

Six Appendices• Suppliers directory• List of Monographs by Functional

Category• List of Related Substances• List of Excipients by ‘E’ number• List of Excipients by ‘EINECS’ number• List of Excipients by ‘CAS’ number

Pharmaceutical Excipients on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices:

For 1 concurrent user, one site – Healthcare € 1.270,– + VAT

For 1 concurrent user, one site – Companies € 1.588,– + VAT


9

British National Formulary (BNF)International Relevance: BNF and BNFC are the gold standard of drug information in English-speaking countries. They are used for constructing national formularies in other countries and to support regulatory work. They provide essential information when treating patients who have been prescribed medicines in the UK. Both resources are completely independent from pharmaceutical industry influence with guidance that is based on best practice and real life evidence.

BNF for Children on MedicinesComplete OnlineYearly subscrip tion fee - 365 days Online access. Base prices:For 1 concurrent user, one site – Healthcare € 905,– + VAT For 1 concurrent user, one site – Companies € 1.129,– + VAT


British National Formulary (BNF) on MedicinesComplete OnlineYearly subscrip tion fee - 365 days Online access. Base prices:For 1 concurrent user, one site – Healthcare € 905,– + VAT For 1 concurrent user, one site – Companies € 1.129,– + VAT

British National Formulary for Children 2019-2020 (BNF for Children)A joint publication of the British Medical Association, the Royal Pharmaceutical Society, the Royal College of Paediatrics and Child Health, and the Neonatal and Paediatric Pharmacists Group A publication of the Pharmaceutical Press

2019. Approx. 1,120 pages. Softcover. € 69,50TN 180046090

BNFC provides essential practical information to all healthcare professionals involved in the prescribing, dispensing, monitoring and administration of medicines to children. It addresses a significant knowledge gap in many areas of paediatric practice by providing practical information on the use of medicines in children of all ages from birth to adolescence. Recommendations in the BNFC have been constructed on the basis of authoritative sources, emerging evidence and best practice guidelines. The content has been carefully validated by a network of paediatric experts and the process is overseen by a paediatric formulary committee.The BNF for Children 2019-2020 has been revised and revalidated to reflect changes in product availability, emerging safety concerns and shifts in clinical practice.

British National Formulary Edited by the Joint Formulary CommitteeA publication of the Pharmaceutical Press

BNF No. 79 (March 2020)79th edition 2020. 1.768 pages. Softcover. € 69,50TN 180046079

BNF No. 78 (September 2019) 78th edition 2019. Approx. 1,640 pages. Softcover. € 69,50 TN 180046078

Aimed at health professionals involved with prescribing, monitoring, supplying and administering medicines, this essential reference offers up-to-date, practical guidance updated every six months.

The BNF details medicines prescribed in the UK, with special reference to their uses, cautions, contraindications, side-effects, doses and relative costs. It enables healthcare professionals to maximize the benefits of drug treatment and minimize the risks, while encouraging good compliance with treatment.

Reference Books

New


Reference Books

Pediatric Injectable DrugsThe Teddy Bear Book

By Stephanie J. Phelps, Kelley R. Lee, Tracy M. Hagemann and A. Jill Thompson.A publication of the American Society of Health-System Pharmacists

11th edition 2018. 850 pages. Softcover. € 187,–ISBN 978-3-7692-6773-0

The 11th Edition of the Teddy Bear Book!

If you work with children, you must have this book. Known as The Teddy Bear Book, it is one of the ASHP’s most recognized and trusted resources dedicated to helping pharmacists treat pediatric patients with injectable drugs.

Every hospital, pharmacist, and nurse that deals with pediatric patients needs this updated reference. The new edition is once again helmed by respected editors Stephanie J. Phelps, PharmD, BCPS,Tracy M. Hagemann, PharmD, FCCP, Kelley R. Lee, PharmD, andA. Jill Thompson, PharmD, includes 15 new monographs and updates based on the latest evidence-backed literature.

Extended Stability for Parenteral Drugs

By Caryn Dellamorte Bing and Anna Nowobilski-Vasilios A publication of the American Society of Health- System Pharmacists

6th edition 2017. 375 pages. Softcover. € 189,– ISBN 978-3-7692-6789-1

Get the support you need to safely extend dating of parenteral drugs beyond the usual 24-hour limit— minimizing waste, lowering medi-cation costs, and enabling optimal patient administration schedules at alternate infusion sites.

The new 6th edition covers all aspects of determining stability, including the changing elastome-ric landscape and the ongoing variability in stability data.

New in the 6th Edition• Nearly all 165 stability mono-

graphs completely updated• Including 11 new stability

monographs• Updated chapters on applying

stability data in patient care and parenteral nutrition

• Previously unpublished data for specific types of infusion devices and containers

• Direct communications from drug and device manufacturers, and a focused review of previously published data from practitioners.

With its expanded coverage, many updates, and new information, Extended Stability provides even more support, making it a “must have” for any practice in which pharmaceutical solutions are prepared and administered.

Calendar for Pharmacists 2021

Created by Dr. Fritz Ferchl. Re-established by Prof. Dr. Wolfgang Hagen-Hein.Continued by Prof. Dr. Werner Dressendörfer and later by Dr. Elisabeth Huwer.Revised by Dr. Oswald Peer, Brixen/Bressanone.

2020. Twelve four-color prints on art paper with calendar and, on the reverse, detailed descriptions and suggestions for further reading. Colored title page. Size 49 by 49 cm. Spiral bound with eye for hanging up the calendar. Explanatory texts in English and German by Dr. Elisabeth and Dr. Oswald Peer, Brixen/Bressanone & Dr. Christiane Baumgärtner, Berlin. Approx. € 89,–ISBN 978-3-7692-7561-2

Through Cabinets of Curiosities, Herbariae and Poison chambers

Our contribution for the year 2021 is a calendar of a special kind. With the selection of the objects we travel to the beautiful city of Bressanone, where there is a jewel of the European pharmacy and pharmaceutical history: thePharmacy Museum Bressanone - Il Museo della Farmacia Bressanone (www.pharmaziemuseum.it).

The example of a Bressanone family of pharmacists tells the exciting and sometimes exciting story of medicines from the realm of minerals, animals and plants. All objects that we present to you are treasures from the traditional collection of the Museo della Farmacia, and our special thanks go to Dr. Oswald Peer. We would like to bring the selected exhibits to you again this year with interesting background information, stories from literature, art and handicrafts.

You will learn something about how elegant pocket spit bottles can be and why they are called 'Blauer Heinrich'. We show you one of the oldest European herbariums with almost a thousand dried and pressed plants, all of which come from the famous botanical garden in Padua. And we take you into the hermetically sealed poison chambers, where substances such as morphine, opiates or snake venom have been kept since ancient times.

Our calendar also shows you how exciting the interior of historical pharmacy cabinets can be, especially when they house more than 200 drawers and what artistic and colourful variations the glass factories have made for the storage of tinctures, medicinal healing waters and herbal essences.

Let yourself be inspired and accompanied this year by phenome-na of curative art worth knowing and seeing, which are still formative for the development of modern pharmaceutical history.

Specials

10

Pediatric Injectable Drugs on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices:

For 1 concurrent user, one site – Healthcare € 520,– + VAT

For 1 concurrent user, one site – Companies € 649,– + VAT


New

Apotheker Kalender 2021Calendar for Pharmacists

New

Errors excepted. Free shipping within Germany, delivery abroad plus € 7,95 shipping per parcel. www.deutscher-apotheker-verlag.de 11

Nutrition

USP Food Chemicals Codex

Internationally recognized standards to verify identity, quality, and purity of food ingredientsThe Food Chemicals Codex (FCC) and associated with USP Reference Materials enables manu-facturers and suppliers to verify the identity, quality, and purity of the food ingredients they buy and sell which help to ensure the overall safety and integrity of the food ingredient supply chain. Monographs in the FCC consist of tests and specifications for identification, assay and impurities, as well as other tests that help describe the purity and quality of the ingredient. FCC standards are reviewed and approved by independent experts. The 12th Edition features:

■ More than 1,250 monographs including - Probiotics & prebiotics - Fats and oils - Flavors - Nutrients - Preservatives - Colorants - Sweeteners - Infant formula ingredients

■ More than 80 new and updated monographs ■ 18 appendices – providing clear, step-by-step guidance for more than 150 tests and assays including: - Lead limit test - Food Fraud Mitigation Guidance - Guidance on Developing and Validating Non-Targeted Testing

■ Helpful information and guidance: - FCC and AOAC/ISO/IUPAC method validation - Comparison of GMP elements from foods and drugs - FCC citations in the US Code of Federal Regulations

Discover how the FCC can work for you! ■ The FCC The FCC is cited over 200 times in the U.S. Code of Federal Regulations and is recognized by regulatory bodies around the world including the US, Argentina, Australia, Brazil, Canada, Israel, New Zealand, Paraguay, and Uruguay.

■ FCC standards are established, evaluated, and revised with scientific rigor in an open, collaborative process involving USP scientists, government representatives, expert volun-teers, and public input. Standards are approved by an Expert Committee that includes technical leaders from industry, academia, and regulatory bodies from around the world.

12th Edition 2020-2021 incl. Supplement 1, 2 and 3

New

Food Chemicals Codex 12th Edition 2020-2021 incl. Supplement 1, 2 and 3A publication of USP, United States Pharmacopeial Convention,Rockwille, MD, USA

Book: 2020. Main work. Approx. 1,678 pages. Hardcover. Including supplement 1 (Sept. 2020), supplement 2 (March 2021), supple-ment 3 (Sept. 2021). € 1076,– [D] ISBN 978-3-7692-7615-2

Online: Rolling subscription. Continually updated. 1 + 2 year subscription available. Price for one seat user: 1 year € 330,–plus VAT 2 years € 555,–plus VAT

New

Strengthening the organism’s self-regula-tion!

Anthroposophic medicines are effective in such a way that they stimulate, strengthen, regulate and harmonise the organism’s own activity in differentiated ways.

Patients and parents do not just need the help of experts, they are experts them-selves. From their own experience as patients or parents, they often know very well which circumstances have triggered or repeatedly trigger the disease to be treated, which symptoms are in the foreground in cases of recurrent illness, which course of the disease is typical in their case and often also what aggravates or alleviates the symptoms. This is the starting point of this publication, the authors provide:

■ Brief descriptions of the symptoms described by patients or their parents

■ Brief descriptions of the medications that are therapeutically suitable and have proven

■ their worth in this constellation ■ Detailed descriptions of their application, which can be adapted to the patient’s

■ respective age and individual circum-stances

GlöcklerSelf Medication in Anthroposophic Medicine

By Georg Soldner, Birgit Emde and Heide Tetzner.Edited by Dr. Michaela Glöckler.2020. 287 pages.E-Book, PDF. € 54,– ISBN 978-3-8047-3748-8

New

New

Nutrition

Food Composition and Nutrition Tables

The comprehensive standard work on the composition of foods – more than 800 food items with over 300 constituents.

This indispensible standard work on the composition of foods, which has been continuously evolving over more than fifty years, has been completely revised, updated and expanded in this new eighth edition.

New in the 8th edition:• More than 20 newly included food items: several cuts of beef | pork and sheep |

various cereals and cereal products | various legumes and wild vegetables | new varieties of tea

• Additional ingredients: phytoestrogens | folic acid | gluten in cereal varieties and cereal products | fatty acids in fish and fish products

The proven concept is not only designed to meet the needs of dieticians and food counsellors, but also provides quick, exhaustive information for everyone involved in the production, marketing and monitoring of foods.

More than 800 foodstuffs and over 300 constituentsThe database of nutrition tables from Souci | Fachmann | Kraut features:• Full-text search: Run instant searches with auto-

complete functions in German, English or French. All data in English.

• Search by constituents: Include as many filter criteria as you want for an exact search.

• Calculator: Select several food products and display nutrient totals on a data sheet.

• Csv-export: Instantly export results from your computer for further calculations.

• Book marks: Mark foods for later use or for the calculator.

Other prices apply for multi-user or for multi-site use. Prices for institutions and libraries can be supplied on request.

Are you interested in purchasing a license to integrate the data in your own system? We would be happy to provide assistance and a price quote.

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SFK.Online I Food Composition and Nutrition TablesAnnual licence fee for a period of twelve months from starting date. Use is limited to a single user at any time at one site:

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A free 10-days-trial at www.SFK.Online

Food Composition and Nutrition TablesFounded by S. W. Souci, W. Fachmann and H. Kraut.On behalf of the German Federal Ministry of Food, Agriculture and Consumer Protection, Berlin Edited by the German Research Centre for Food Chemistry, Garching Compiled by Dr.Gaby Andersen

Book: 8th revised and completed edition 2016. XXXII, 1,263 pages. Hardcover. € 156,– ISBN 978-3-8047-5072-2

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2017 / 2018 - Deutscher Apotheker Verlag · The British Pharmacopoeia 2018 supersedes the BP 2017....

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