2019 i 2020 - deutscher-apotheker-verlag.de · dosage forms, drug substances, excipients,...

InternationalPharmaceutical and Medical

Publications

2019 I 2020

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

Pharmacopoeia

Earliest access to all European quality standards that come into effect on 1 January 2020!

Electronic version: First year subscription provides access until 31 December 2020 to the content of main work 10.0 and first 2 cumulative updates, 10.1 and 10.2, as well as to the Ph. Eur. online archives for 1 named user.

Including:• Direct links to texts• Improved search query management• Improved visibility of changes (for revised and corrected texts)

NEW electronic version providing:• Completely cumulative versions, bilingual (English and French), with new features and direct access to

complementary information (Knowledge Database).• Access to the Ph. Eur. online website from all recent common operating systems (tablet and smartphone

friendly).• Application fully compatible with recent Windows and Linux operating systems (Mac coming soon). It allows

installation of the application to 1 computer and to 1 USB stick, for online or offline use, for easy access while on the move or in environments where the use of the book or the website would not be possible or would be impractical.

Multiuser prices on demand. Please ask for an offer.

The single reference for medicines and substances for pharmaceutical use in Europe The European Pharmacopoeia (Ph. Eur.) is Europe’s legal and scientific benchmark for pharmacopoeial standards which contribute to delivering high quality medicines in Europe and beyond. The Ph. Eur. is applicable in 38 European countries and beyond.

It delivers crucial information earlier than any other pharmacopoeia. With 114 new and 683 revised texts, approximately 30% of the content is new or revised compared to Edition 9.0. It contains 2,420 monographs, 374 general texts (including general monographs and methods of analysis) and around 2,780 descriptions of reagents. The texts 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, substances or preparations for pharmaceutical use of chemical, animal, human or herbal origin, homoeopathic preparations and stocks, antibiotics, as well as dosage forms and containers. It also applies to biologicals, blood and plasma derivatives, vaccines and radiopharmaceutical preparations.

The new 10th Edition consists of 3 initial volumes (10.0) complemented by 8 updates issued three times a year to create collection of 8 supplements (10.1 to 10.8) until 2022. Access to Ph. Eur. online archives is included to all users with an up-to-date subscription (print or electronic). Book version: Available in English or French. The subscription first year contains 3 initial volumes (10.0) and the first 2 non-cumulative supplements, 10.1 and 10.2. It also provides access to the Ph. Eur. online archives until 31 December 2020. For the convenience of users, direct access to complementary information (Know-ledge Database) is included for each monograph and general chapters through a data matrix code.

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

Book: Hardcover. On continuation.

Subscription to the 10th Edition first year (3 initial volumes and supplement 10.1 and 10.2): 2019

English language. € 577,80 ISBN 978-3-7692-7453-0

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

Special price for Package electronic version + book: 2019

1 electronic version licence with access to 10.0–10.2, first year. (Bilingual: English and French). 1 user. + Book Subscription to 10th Edition first year (10.0–10.2): € 983,10 (instead of € 1.220,40)

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

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

Electronic version: One licence (bilingual: English l French) incl. Archive. Allows access for 1 named user. Price per licence. Access to 10.0–10.2: € 540,– + VAT Multiuser prices on demand.

www.edqm.eu

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January 2020

July 2020

October 2020

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July 2021

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1 January2021

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Publication Schedule 10th Edition

New

European Pharmacopoeia 10th Edition

New

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

Pharmacopoeia

www.deutscher-apotheker-verlag.de

USB Stick: 2019. (November 2018).Yearly single user subscription fee. € 1.070,– + VAT ISBN 978-3-7692-7415-8

Online: Rolling subscription. 365 days access. Continually updated. Price per ID: € 945,– + VAT

USP 42 – NF 37 U.S. Pharmacopeia (USP 42) & National Formulary (NF 37)A publication of the United States Pharmacopeial Convention

Book: 2018. Slipcase containing: Main work. 5 volume books. Hardcover. (November 2018). Approx. 8200 pages.Including Supplement 1: (February 2019). Supplement 2: (June 2019)Annual subscription. English language € 1.122,–. ISBN 978-3-7692-7330-4

Also available in Spanish language at the same price (March 2019).

USP-NF 2019United States Pharmacopeia (USP) and National Formulary (NF)

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

USP standards are used in more than 140 countries around the world. • More than 4,900 monographs with specifications for identity, strength, quality, purity, packaging, and

labeling for substances and dosage forms.• More than 350 general chapters providing clear, step-by-step guidance for assays, tests, and procedures• Focus-specific charts and a combined index help you find the information you need• Helpful sections on reagents, indicators, and solutions, plus reference tables• Includes new General Chapter <800> Hazardous Drugs—Handling in Healthcare Settings

The USP–NF offers convenient, comprehensive information for all phases of producing quality prescription, nonprescription, and compounded medicines; excipients; biologics; medical devices; and dietary supple-ments. It is essential for quality control, quality assurance, regulatory/compendial affairs, research and development, method development/analytical services, and corporate management.

USP–NF monographs and methods can help to• Ensure compliance with required U.S. quality standards• Work to world-recognized standards of precision and accuracy• Validate test results against proven benchmarks• Establish and validate in-house standard operating procedures, and specifications• Expedite new product development and approvals

An ISO certified Spanish translation (certified to ISO 17100:2015) of USP-NF compendial content is available in print as the Spanish edition.

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

The USP 42 – NF 37 is official: Main Edition – May 1, 2019 Supplement 1 – August 1, 2019 Supplement 2 – December 1, 2019


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) Edited by the British Pharmacopoeia CommissionA publication of The Stationery Office

Book: 2019. Approx. 6,700 pages. Slipcase containing 6 volume books + Download (single user*)+ Online access (single user*). € 1.478,– Prepublication price valid until 31 October 2019: € 1.298,–ISBN 978-3-7692-7467-7

New

New

New, legally enforced standards, available from 1 August 2019. 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.

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 2015. 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

Newonline

Print: Complete work including 15th Supplement 2018 2,318 pages. 2 ringbinders. Loose-leaf serial. € 380,– ISBN 978-3-8047-5081-4

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.


Martindale The Complete Drug Reference

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

For 1 concurrent user, one site – Healthcare € 2.171,– + VAT

For 1 concurrent user, one site – Companies € 2.713,– + 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• Disease Management• 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• Stedman's Medical Dictionary• 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

Reference Books

Quote and a free 30-days-trial are available on demand.

39th Edition

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

39th revised and updated edition 2017. 2 volumes in slipcase. 4,688 pages. Hardcover. € 674,–TN 180046063

Martindale: The Complete Drug Reference provides unbiased and evaluated information on drugs and medicines in use around the world. It is prepared by an experienced team of pharmacists and life scientists who use their professional expertise to select the most clinically relevant and appropriate information from reliable published sources, to provide an unbiased and evaluated digest of the literature.

Improvements for the 39th edition:• Over 130 new monographs, including:• Lumacaftor: a cystic fibrosis transmembrane conductance regulator

(CFTR) protein corrector • Pitolisant: a central stimulant used in the treatment of narcolepsy • Rolapitant: a neurokinin-1 receptor antagonist that is used for the prevention of nausea and

vomiting associated with cancer chemotherapy • Umeclidinium Bromide: a quaternary ammonium antimuscarinic used as a bronchodilator in the

treatment of reversible airways obstruction • New Hepatitis C treatment table and drugs including ledipasvir, ombitasvir, paritaprevir, and

dasabuvir• Coverage of proprietary preparations in 43 countries including Australia, China, UK, and USA, revised

and updated

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

This package contains two hardback volumes presented in a slipcase with:• Over 6,300 drug monographs (and over 7,500 online, accessible via a subscription to Medicines

Complete)• Over 185,000 preparations (and over 27,0000 via MedicinesComplete)• Over 54,000 reference citations • Over 20,000 (and 28,000 online, via MedicinesComplete ) manufacturers and distributors• Proprietary preparations from 43 countries and regions • Nearly 700 treatment reviews, with references from the published literature • Information to help you identify medicines, the local equivalent and the manufacturer• Herbals, diagnostic agents, radiopharmaceuticals, pharmaceutical excipients, toxins, and poisons as

well as drugs and medicines

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

Reference Books

7

AHFS Drug Information® 2019

AHFS Drug Information 2019American Hospital Formulary Service Drug InformationA publication of the ASHP American Society of Health-System Pharmacists

2019. 3,840 pages. Softcover. € 489,–ISBN 978-3-7692-7418-9

Protect the patients and practice with the most comprehensive, authoritative drug information.

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. The 2019 edition is backed by over 60 years of in-depth, unbiased drug coverage—delivering authoritative data for compendia, citations, compliance and more.

Information on prescription, OTC, ophthalmic, and dermatologic drugs is evidence-based, reviewed by subject matter experts, and supported by nearly 90,000 references. Every year’s edition is updated with an expanded number of monographs, which can be found on the For Subscribers section with the password found in the preface of each new edition. It includes therapeutic recommendations supported by primary research, extensive dosage and admini-stration information, extensive off-label uses and related dosing options.

AHFS DI on MedicinesComplete Online

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

For 1 concurrent user, one site – Healthcare € 1.920,– + VAT For 1 concurrent user, one site – Companies € 2.400,– + VAT

Quote and a free 30-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

Updates for this edition include:

• Expanded and revised content throughout, featuring critical new monograph updates every year

• Important updated monographs and references related to revised therapeutic guidelines, including revised recommendations for treatment of fungal infections (such as Candida auris infections) and chronic hepatitis C

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

• Dedicated coverage to orphan products

New

• Interactions, adverse reactions, and cautions, including ongoing revisions addressing opiate safety issues and their role in pain manage-ment

• Therapeutic recommendations supported by evidence from primary research

• Extensive dosage and administration information

• Pharmacology and pharmacokinetics• Prescription, OTC, ophthalmic and dermato-

logic drugs• Extensive off-label uses and related dosing

options• Vaccines and other immunizing agents

Drug monographs in AHFS DI are thoroughly researched by drug information pharmacists and professional editorial and analytical staff. Authors incorporate clinical research findings, guidelines, and FDA-approved labeling into the monographs. The information also reflects the expertise of leading medical scientists, physicians, pharmacists, pharmacologists, and other clinicians, and incorporates the latest therapeutic recommendations from groups like the US Centers for Disease Control and Prevention (CDC), the National Institutes of Health (NIH), the American Academy of Pediatrics, the American Heart Association, and many others.

New


Handbook on Injectable Drugs on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices:For 1 concurrent user, one site – Healthcare € 1.443,– + VAT For 1 concurrent user, one site – Companies € 1.803,– + 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

Stockley's Drug Interactions

Stockley’s Drug Interactions remains the world’s most comprehensive and authoritative international reference book on drug interactions. Based upon thousands of published papers and reports:• Covers interactions between therapeutic drugs, proprietary

medicines, herbal medicines, foods, drinks, and drugs of abuse• Contains in-depth yet concise monographs in an easy-to-read

format• Provides comprehensive details of the clinical evidence for the

interactions under discussion, an assessment of their clinical importance, and clear guidance on managing the interaction in practice

• Has a brief summary of the interaction in each monograph – perfect for the busy healthcare professional

• Is fully referenced throughout• Contains almost 4,500 monographs• Is global in coverage – inclusion of drugs used worldwide

New in the 11th edition:• Over 350 new monographs added• Many existing monographs have been reviewed, revalidated,

and updated• A comprehensive update and restructure of the chapter on

Antidiabetic drugs, in-line with published literature• Addition of new advice regarding the concurrent use of aliskiren,

ACE inhibitors, and angiotensin-II receptor antagonists• An updated list of drugs that have a risk of prolonging the QT

interval• The addition of new drugs, including apixaban, apremilast,

dolutegravir, lomitapide, mirabegron, the NS5A inhibitors (daclatasvir, ledipasvir, ombitasvir), the NS5B inhibitors (dasabuvir, sofosbuvir), the sodium-glucose co-transporter-2 inhibitors (canagliflozin, dapagliflozin, empagliflozin), and telavancin

Edited by Claire L. PrestonA publication of the Pharmaceutical Press

Book: 11th edition 2016. 1,840 pages. Hardcover. € 259,– TN 180046050

A source book of interactions, their mechanisms, clinical importance and management.

Stockley‘s Drug Interactions on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices: For 1 concurrent user, one site – Healthcare € 1.732,– + VAT For 1 concurrent user, one site – Companies € 2.165,– + VAT

Stockley‘s Herbal Medicines Interactions on MedicinesComplete Online

Yearly subscrip tion fee - 365 days Online access. Base prices: For 1 concurrent user, one site – Healthcare € 620,– + VAT For 1 concurrent user, one site – Companies € 773,– + VAT


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.

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 € 1.254,– + VAT

For 1 concurrent user, one site – Companies € 1.566,– + 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 € 855,– + VAT For 1 concurrent user, one site – Companies € 1.069,– + VAT


British National Formulary (BNF) on MedicinesComplete OnlineYearly subscrip tion fee - 365 days Online access. Base prices:For 1 concurrent user, one site – Healthcare € 855,– + VAT For 1 concurrent user, one site – Companies € 1.069,– + VAT

British National Formulary for Children 2018-2019 (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

2018. 1,120 pages. Softcover. € 69,50TN 180046089

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 2018-2019 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. 75 (March 2018)75th edition 2018. 1,600 pages. Softcover. € 69,50TN 180046075

BNF No. 76 (September 2018) 76th edition 2018. 1,640 pages. Softcover. € 69,50TN 180046076

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

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

Reference Books

Pediatric Injectable DrugsThe Teddy Bear BookBy 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

It’s Time for a new 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.

2018. 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. € 78,–ISBN 978-3-7692-7151-5

Through the year with the Calendar for Pharmacists 2019

The Calendar for Pharmacists 2019 delights the reader with 12 attractive images and their fascinating background stories. It is a companion for the whole year with a fresh new topic each month.

Well-known museums such as German Pharmacy Museum in Heidelberg, the Dresden State Art Collections and the Brandenburg Pharmacy Museum in Cottbus as well as private collections of pharmacy history have opened their doors to present magnificent objects, some of which are shown to the general public for the very first time.

Each month’s pictures fascinates us in its own way, from the costly Baroque travel medicine chest with its mother-of-pearl marquetry and gilt jars and bottle caps to the 18th Century verdigris sphere suspended like a planet in the centre of the calendar plate, from the graceful Gründerzeit dispensary of the Angel Pharmacy in Chemnitz to the cheerful fish dancing their watery ballet around a fishing boat in a playful window display for the strengthening power of cod liver oil from the mid-20th Century.

The images are as varied as the centuries-old, tradition- steeped history of pharmacy, and the viewer is invited to discover new details at each glance. The pictures are accompanied by fascinating, sometimes astounding and often humorous background stories that tell the multifaceted history of pharmacy.

Calendar for Pharmacists 2019

Founded by Dr. Fritz Ferchl.

Continued by Prof. Dr. Wolfgang Hagen-Hein and later by Prof. Dr. Werner Dressendörfer. Revised by Dr. Elisabeth Huwer.

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 € 504,– + VAT

For 1 concurrent user, one site – Companies € 630,– + VAT


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

USP Food Chemicals Codex

Food Chemicals Codex 11th Edition 2018-2019 incl. Supplement 1, 2 and 3A publication of USP, United States Pharmacopeial Convention, Inc., Rockwille, MD, USA

Book: 2018. Main work. 1,678 pages. Hardcover. Including supplement 1 (Sept. 2018), supplement 2 (March 2019), supplement 3 (Sept. 2019). € 849,– [D] ISBN 978-3-7692-7212-3

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

USP Dietary Supplements Compendium 2015The Authoritative ReferenceA publication of USP, United States Pharmacopeial Convention, Inc., Rockwille, MD, USA

2nd edition 2015. 3,712 pages. 2 volume set. Hardcover. € 530,– ISBN 978-3-7692-6442-5

The comprehensive, authoritative reference dedicated to dietary supplements This unique reference combines the USP–NF standards for dietary supplements with information from the Food Chemicals Codex. Significantly expanded and updated it contains comprehensive specifications, established methods, and industry information helpful for producing and authenticating the quality of dietary supplements and their ingredients.

Two Volume set. One indispensable quality resource.• 75 new dietary supplement monographs (nearly

500 in all) from USP 38-NF 33• 27 new General Chapters• More than 175 excipient monographs• Over 200 Food Chemicals Codex (FCC) monographs• Over 40 new and revised DSC admission evaluations• Includes over 150 added pages of color plates and

illustrations

Essential dietary supplement information – under one cover for• Developing, manufacturing, and testing new products • Qualifying raw materials • Preparing for internal QC and GMP audits • Reference tables, charts, and guidance documents

from the US FDA, US FTC, APHA, and industry • Conducting in-process and batch-release tests • Accurately packaging, labeling, and storing products

USP Dietary SupplementsCompendium 2015

Internationally recognized standards to verify identity, quality, and purity of food ingredientsThe Food Chemicals Codex (FCC) in conjunction with USP Reference Materials enables manufacturers and suppliers to verify the identity, quality, and purity of the food ingre-dients they buy and sell. 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. The Eleventh Edition features:

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

■ More than 45 new and updated monographs ■ 18 appendices – providing clear, with step-by-step guidance for 150 tests and assays ■ 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 is cited over 200 times in the US 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 volunteers, and public input. Standards are approved by an Expert Committee that includes technical leaders from industry, academia, and regulatory bodies from around the world.

■ The FCC is updated through the FCC Forum —an online collaborative process that lets you help shape food ingredient standards!

Nutrition

11th Edition 2018-2019 incl. Supplement 1, 2 and 3

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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