Pharmacopoeias
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British Pharmacopoeia 2009.
British Pharmacopoeia Commission TSO (The Stationery Office). due
September 2008.
The British Pharmacopoeia (BP) 2009 is the authoritative, current
collection of standards for UK medicinal substances and the official source of
all UK pharmaceutical quality standards. It is an essential reference for
anyone involved in pharmaceutical research, development, manufacture and
testing, and plays a vital role in ensuring that all medicinal substances on
the UK market meet standards of safety, quality and efficacy.
The BP comprises monographs, which set out the mandatory standards for active substances, excipients and formulated preparations, together with supporting General Notices, Appendices (test methods, reagents, etc) and Reference Spectra. Detailed information and guidance on various aspects of current pharmacopoeial policy and practice are provided in the Supplementary Chapters of the BP.
The BP is supplied in a variety of formats designed for ease of use and a wide range of applications. The hard copy edition comprises a five-volume boxed set containing the BP in four volumes and the BP (Veterinary) volume, plus single user access to the BP Online via www.pharmacopoeia.co.uk, the dedicated BP website. The online format is easy to network, allowing access for a specified number of users or across an entire organisation site.
Following registration - using the ID code supplied with the hard copy - customers will be granted a single user licence to access BP on-line and will have the option to receive the CD-ROM, which contains the whole of the current British Pharmacopoeia.
Key Features:
ISBN: 011322799X; 9780113227990. 5 volumes. $1800.00, 2-5 users $4800 plus you must also purchase the printed version for the first license.
European
Pharmacopoeia 6th Edition: Author: Council of Europe (COE) - European Directorate for the Quality of
Medicines: The 6th edition of the European Pharmacopoeia comes into force on the 01
January 2008 and consists of a two-volume main edition. It will been updated on
a regular basis with one supplement following in October 2007, three in 2008 and
2009 and the remaining supplement in 2010 to create a collection of eight non
cumulative supplements.
Key features:
ISBN 10: 9287160546; ISBN 13: 9789287160546. $570. Supplements 6.1 and 6.2 are now available, 6.3 due June, 6.4-6.8 will be published in the next two years. Each supplement will be approximately $154.00; CDROM version 2009 supplement pack 6.3-6.5, $600.00 for subscribers.
British Pharmacopoeia (BP) 2008. September 2007. The British Pharmacopoeia (BP) 2008 is the authoritative, current collection of standards for UK medicinal substances and the official source of all UK pharmaceutical quality standards. It is an essential reference for anyone involved in pharmaceutical research, development, manufacture and testing, and plays a vital role in ensuring that all medicinal substances on the UK market meet standards of safety, quality and efficacy. The BP comprises monographs, which set out the mandatory standards for active substances, excipients and formulated preparations, together with supporting General Notices, Appendices (test methods, reagents, etc) and Reference Spectra. Detailed information and guidance on various aspects of current pharmacopoeial policy and practice are provided in the Supplementary Chapters of the BP. The BP is supplied in a variety of formats designed for ease of use and a wide range of applications. The hard copy edition package comprises a boxed five volume set containing BP in four volumes and the BP (Veterinary) volume, plus single user access to the BP on-line via pharmacopoeia.co.uk, the dedicated BP website. The online format is easy to network, allowing access for a specified number of users or across an entire organisation site. Following registration using the ID code supplied with the hard copy, customers will be granted a single user licence to access BP on-line and will have the option to receive the CD-ROM that contains the whole of the current British Pharmacopoeia. For the first time, the BP is available in an e-book format to purchasers of the hard copy BP 2008. The content of the British Pharmacopoeia can be downloaded to portable PDA, laptop, PC or smartphone.
· A significant number of new UK monographs
· All European Pharmacopoeia 5th edition material up to and including Supplement 5.8 integrated into the text of BP 2008
· Acid-Base Indicators in color
· Value-for-money networking with full technical support from TSO, the publisher of the BP
· On–line version delivers the complete text of the British Pharmacopoeia and European Pharmacopoeia standards to your PC.
www.pharmacopoeia.co.uk is regularly updated and includes information on monograph development and contact points. Access to the electronic BP 2008: As part of the BP 2008 package customers will be supplied with a unique I.D. code which grants them single user access to the BP online via http://pharmacopoeia.co.uk. In addition, as part of the BP package, they will receive separately the BP 2008 CD-ROM by supplying the same I.D. code to Balogh International Inc. If additional users in their organization require simultaneous access to the BP 2008 they will require a network license. Network licenses can be set up for any range of users, from a single user to company-wide access. Accessing the networked pharmacopoeia through workstations represents a substantial saving on purchasing multiple print edition BP 2008 packages. ISBN 9780113227501. estimated $1800 plus $40 insured UPS shipping Continental USA, inquire elsewhere. 2-5 USER License $6700, includes printed version. Shipping is same.
Dictionnaire VIDAL. 2008. The 84th edition of the VIDAL Drug Compendium lists more than 5000 drugs and 4900 consumer healthcare products. Each product monograph includes the official prescription information provided in the Summary of Product Characteristics (SPC) issued by the French Health Products Safety Agency (Afssaps). 3136 pages. in French only! Parution : annuelle (fin janvier) comprenant le Dictionnaire + le fascicule Informations Pratiques + 2 mises à jour cumulatives (mai et octobre). $400.00
La référence en matière d'information sur le
médicament. Avec plus de 5000 médicaments et 4900
produits de parapharmacie référencés pour cette 82e édition, le Dictionnaire
VIDAL constitue l'ouvrage indispensable des professionnels de Santé dans le
cadre de leur pratique quotidienne. La monographie reprend l'information
officielle des Résumés des Caractéristiques du Produit (RCP), issue de l'Agence
Française de Sécurité Sanitaire des Produits de Santé (AFSSAPS).
Consultable facilement à partir d'une classification alphabétique, la
monographie structurée en rubriques apporte une information complète sur le
médicament.
Indissociable du Dictionnaire VIDAL, le nouveau fascicule Informations
Pratiques contient notamment les différentes classifications des médicaments
ainsi que de nombreuses annexes complémentaires.
Le Dictionnaire est composé de 5 sections de couleur différentes :
Section BLANCHE
Classement alphabétique des monographies de médicaments regroupant :
- 5000 médicaments
- 3300 monographies, pouvant être composées de 19 rubriques selon le plan
européen du RCP.
Section SAUMON
Index général alphabétique des monographies des produits de parapharmacie
- 4900 produits de parapharmacie classés par ordre alphabétique dans 6
catégories spécifiques(accessoires, désinfection, diététique, hygiène et
cosmétologie, réactifs et tests, thermalisme)
- représentant 1250 monographies.
Section BLEUE
Classement alphabétique des médicaments par principe actif (DCI, DCF ou
dénomination usuelle).
Section JAUNE
Classification des médicaments par famille pharmacothérapeutique.
Section VERTE
Répertoire alphabétique des établissements :
- près de 600 établissements : laboratoires pharmaceutiques, parapharmaceutiques,
stations thermales...
- Liste exhaustive des médicaments et des produits par établissement.
Le fascicule Informations Pratiques comprend les 3 sections BLEUE, VERTE et JAUNE mais également les sections ROUGE et GRISE ainsi que de nombreuses annexes complémentaires utiles au praticien :
Section ROUGE
Index général des spécialités.
Section GRISE
Liste des génériques issus du répertoire officiel de l'AFSSAPS.
ANNEXES COMPLEMENTAIRES
- Modalités de prescription et de délivrance des médicaments : prescription des
affections de longue durée, prescription des médicaments d'exception,
médicaments à prescription restreinte,...
- Règles et recommandations thérapeutiques : calendrier vaccinal,
recommandations sanitaires pour les voyageurs,...
- Adresses utiles : centres de pharmacovigilance, centres anti-poison et centres
de toxicovigilance, centres antirabiques...
The Japanese Pharmacopoeia Fifteenth Edition. (JP XV). Official from
March 31, 2007 .
Edited by Society of Japanese Pharmacopoeia.
2007.
The revised JP XV in English language comprises
the following items in order: The Ministry of Health, Labour and Welfare
Ministerial Notification; Contents; Preface; General Notices; General Rules for
Crude Drugs; General Rules for Preparations; General Tests, Processes and
Apparatus; Official Monographs, including Monographs for Crude Drugs; Infrared
Reference Spectra; Ultraviolet-visual Reference Spectra; General Information;
Atomic Weight Table (2004) and Standard Atomic Weights 2004 as Appendix ; and
Cumulative Index (English, Latin and Japanese titles). Main features and
revisions of this book are:
English and Latin titles of drugs were based on International Nonproprietary Names for Pharmaceutical Substances, and chemical names were based on Rules of International Union of Pure and Applied Chemistry (IUPAC). General Rules for Preparations which were revised are General Notices for Preparations; Extracts; Capsules; Transdermal Systems (new addition); Tablets; Injections; Plasters and Pressure Sensitive Adhesive Tapes; and Arrangements for others. In General Tests, Processes and Apparatus, “Content Uniformity Tests” and “Mass Variation Tests” were combined and renames as “Uniformity of Dosage Units”. General Tests, Processes and Apparatus which were revised are Ammonium Limit Test; Arsenic Limit Test; Crude Drugs Test; Disintegration Test; Dissolution Test; Insoluble Particulate Matter Test for Injections; Melting Point Determination; Microbial Assay for Antibiotics; Microbial Limit Test for Crude Drugs; Powder Particle Size Determination; Residue on ignition Test; Specified Surface Area Determination; and Test Methods for Plastic Containers, and which were deleted are Absorbance Ratio Method; Methoxyl Assay; Paper Chromatography, and Volatile Contaminations in Ethanol.
Official Monographs provides 1483 articles, including 102 articles newly added and 8 articles deleted. 1820 pages, ISBN978-4-8408-0974-0 C3047, Hardbound, A4 format. $950.00
The
International Pharmacopoeia, Fourth Edition. World Health Organization (WHO).
2007. 'The International Pharmacopoeia - Fourth Edition' consolidates the texts
of the five separate volumes of the third edition. Certain additions and
amendments have been made to the notices in order to clarify the interpretation
of the Pharmacopoeia and to facilitate application of the requirements by the
user. This fourth edition will include all the monographs in the third edition
together with new monographs for didanosine, indinavir sulfate, nelfinavir
mesilate, nevirapine, ritonavir, saquinovir, saquinovir mesilate. All the
monograph texts are brought together in one section and the method texts in
another. Each of these major sections are divided into appropriate sub-sections
and the method texts are numbered for ease of cross-reference. Method texts that
have been updated include, for example, the text on high performance liquid
chromatography [HPLC]. This has been revised to clarify certain technical terms
and to add advice on adjustment of chromatographic conditions, as recommended by
the WHO Expert Committee on Specifications for Pharmaceutical Preparations in
October 2004. 924156301X; 9789241563017. $460.00
German Homoeopathic Pharmacopoeia. 2006. 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 583 monographs and 286
general texts including reagents, vehicles and excipients, analytical and
the very important 54 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 harmonized with the European Pharmacopoeia (Ph.
Eur.) and the German Pharmacopoeia (DAB). Each monograph is uniformly
structured, listing (wherever applicable)
* origin
* description
* characteristics
* identification
* purity tests and
* assays
and providing information on the basic dosage forms and their
* manufacture
* characteristics
* identification
* purity tests
* assays and
* storage.
The loose-leaf format makes it easy for the user to keep his collection up
to date. ISBN 978-3-8047-5037-1. $626.40; new supplement $165.60
Pharmacopoeia of the People's Republic of China 2005. English Edition. Author: Pharmacopoeia Commission. Published: Nov 2005.
This
eighth Edition of the 'Pharmacopoeia of the People's Republic of China
2005', is an official and authoritative compendium of drugs. It covers most
traditional Chinese medicines, most western medicines and preparations,
giving information on the standards of purity, description, test, dosage,
precaution, storage, and the strength for each drug. This 2005 Edition
contains up to 3214 monographs of drugs, with 525 new admissions in total.
Published in three volumes:
Volume III - Contains biological products.
ISBN 011989663X.
$1400.00
HARDCOVER
APF20 Australian Pharmaceutical Formulary and Handbook. due March 2006.
Major sections in this latest edition include:
• Dispensing Advice – includes information on abbreviations, extemporaneous
dispensing, formulary (including paediatric doses and children’s formulary),
methadone and buprenorphine dispensing.
• Clinical Notes – a new and comprehensive clinical notes section for drugs,
including counselling and medication review ‘trigger points’.
• Clinical and Therapeutic Information – a range of information including
healthy weight ranges, dosing in renal impairment, medicines and urinary
incontinence, modification of oral formulations, pharmacokinetic data,
medicines, drugs and breastfeeding, comparing insulin preparations, wound
management and more.
• Complementary Medicines – reorganised to provide information on uses,
contraindications and interactions for each complementary medicine.
• Health Resources – includes information on infectious disease exclusion
periods, travel health, drugs in sport, food additives and more.
• Standards and Guidelines – the most comprehensive guidance to contemporary
professional practice in Australia of any text
$250.00
The MIMS Annual is the flagship product of MIMS Australia. It is this publication that has made MIMS the byword for accurate, reliable, comprehensive and independent medicines information. This has replaced the Australian Prescription Products Guide
The MIMS Annual is:
approximately $400 (depending on current exchange rate). hardcover, updated July of every year.
THE JAPANESE PHARMACEUTICAL CODEX 1997
Preface
General Notices
JPC 1997
Part I：Pharmaceutical Active Ingredients
PartII：Pharmaceutical Preparations
General Tests, Processes and Apparatus
（1）Reference Standards
（2）Reagents and Test Solutions
（3）Standard Solutions for Volumetric Analysis
（4）Standard Solutions
Index . 1848 pp. hardcover. $1500.00
Pharmacopee Francaise. set of main edition and most current supplements (2007): $1200.00
Pharmacopee Francaise. 2007 update, incorporates 2006 updates and includes CDROM. estimated $225.00
List medicinal Plants. Edition 10th. 2005. The “list of the medicinal plants” has not been revised since 1993. The update is essential from a therapeutic point of view (evolution of certain indications, introduction of new species, obsolete character of some others) and legislature (appearance of the food complements and harmonization of the European Pharmacopeia and the French Pharmacopeia). List A (traditional use) was considerably reduced and list B (potential adverse effects) was increased. This edition presents for the first time the glossary of the terms of botany. 84 pp. $100.00
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