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Book D  nominations Communes Internationales  DCI  Pour Les Substances Pharmaceutiques

Download or read book D nominations Communes Internationales DCI Pour Les Substances Pharmaceutiques written by Organizacion Mundial de la Salud OMS and published by . This book was released on 1996 with total page 885 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Current Catalog

    Book Details:
  • Author : National Library of Medicine (U.S.)
  • Publisher :
  • Release : 1993
  • ISBN :
  • Pages : 1628 pages

Download or read book Current Catalog written by National Library of Medicine (U.S.) and published by . This book was released on 1993 with total page 1628 pages. Available in PDF, EPUB and Kindle. Book excerpt: First multi-year cumulation covers six years: 1965-70.

Book WHO Expert Committee on Specifications for Pharmaceutical Preparations

Download or read book WHO Expert Committee on Specifications for Pharmaceutical Preparations written by World Health Organization and published by World Health Organization. This book was released on 2008-05-05 with total page 151 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Expert Committee on Specifications for Pharmaceutical Preparations works towards standards and guidelines for medicines' quality assurance. The forty-second meeting adopted 11 new monographs for inclusion in The International Pharmacopoeia (Ph. Int.) and seven related new International Chemical Reference Standards (ICRS). The specifications currently developed are internationally applicable test methodologies for antimalarial, antituberculosis, antiretroviral and specifically also medicines for children. The main principles for selection of INNs for biologicals were endorsed. In order to serve the WHO-managed Prequalification Program, two new procedures were adopted, namely on prequalification of intrauterine devices (IUDs) and of male latex condoms, together with a new guidance on the assessment of active pharmaceutical ingredients for use in medicines.--Publisher's description.

Book Advice Concerning the Addition of Certain Pharmaceutical Products and Chemical Intermediates to the Pharmaceutical Appendix to the Harmonized Tariff Schedule of the United States  Inv  332 476

Download or read book Advice Concerning the Addition of Certain Pharmaceutical Products and Chemical Intermediates to the Pharmaceutical Appendix to the Harmonized Tariff Schedule of the United States Inv 332 476 written by and published by DIANE Publishing. This book was released on with total page 121 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book WHO Drug Information

    Book Details:
  • Author :
  • Publisher : World Health Organization
  • Release : 2021-04-08
  • ISBN : 9240022805
  • Pages : 355 pages

Download or read book WHO Drug Information written by and published by World Health Organization. This book was released on 2021-04-08 with total page 355 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book WHO Drug Information

Download or read book WHO Drug Information written by World Health Organization and published by World Health Organization. This book was released on 2024-07-02 with total page 239 pages. Available in PDF, EPUB and Kindle. Book excerpt: Overview The first issue of Volume 38, includes Consultation Documents: - fluodeoxyglucose (18F) injection (fluodeoxyglucosi (18F) solution injectabilis) ATC/DDD Classification - ATC/DDD Classification (Temporary) and ATC/DDD Classification (Final) The first issue of Volume 38, concludes with: International Nonproprietary Names (INN) Recommended List No. 91

Book National Library of Medicine Current Catalog

Download or read book National Library of Medicine Current Catalog written by National Library of Medicine (U.S.) and published by . This book was released on with total page 1044 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book WHO Expert Committee on Specifications for Pharmaceutical Preparations

Download or read book WHO Expert Committee on Specifications for Pharmaceutical Preparations written by World Health Organization and published by World Health Organization. This book was released on 2019-05-29 with total page 303 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear independent and practical standards and guidelines for the quality assurance of medicines. Standards are developed by the Committee through worldwide consultation and an international consensusbuilding process. The following new guidelines were adopted and recommended for use: Procedure for development of the WHO medicines quality assurance guidelines; Guidelines on Good Manufacturing Practices (GMP) for heating ventilation and air-conditioning systems (HVAC) ? illustrative part; Guidance on GMP for Validation including the general main text analytical procedure validation validation of computerized systems and qualification; in the area of interchangeability of multisource medicines: the Protocol to conduct equilibrium solubility experiments for the purpose of biopharmaceutics classification systembased classification of active pharmaceutical ingredients for biowaiver; Guidelines on Import Procedures for pharmaceutical products; and the Good Practice Guidance document on implementing the collaborative procedures. All of the above are included in this report and recommended for implementation.

Book New Serial Titles

Download or read book New Serial Titles written by and published by . This book was released on 1986 with total page 2532 pages. Available in PDF, EPUB and Kindle. Book excerpt: A union list of serials commencing publication after Dec. 31, 1949.

Book Drug Literature  a Factual Survey on  The Nature and Magnitude of Drug Literature

Download or read book Drug Literature a Factual Survey on The Nature and Magnitude of Drug Literature written by National Library of Medicine (U.S.) and published by . This book was released on 1963 with total page 188 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Handbook of Terminology Management  Basic aspects of terminology management

Download or read book Handbook of Terminology Management Basic aspects of terminology management written by Sue Ellen Wright and published by John Benjamins Publishing. This book was released on 1997 with total page 385 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Terminology Management is a unique work designed to meet the practical needs of terminologists, translators, lexicographers, subject specialists (e.g., engineers, medical professionals, etc.), standardizers and others who have to solve terminological problems in their daily work.In more than 900 pages, the Handbook brings together contributions from approximately 50 expert authorities in the field. The Handbook covers a broad range of topics integrated from an international perspective and treats such fundamental issues as: practical methods of terminology management; creation and use of terminological tools (terminology databases, on-line dictionaries, etc.); terminological applications.The high level of expertise provided by the contributors, combined with the wide range of perspectives they represent, results in a thorough coverage of all facets of a burgeoning field. The lay-out of the Handbook is specially designed for quick and for cross reference, with hypertext and an extensive index.See also "Handbook of Terminology Management" set (volumes 1 and 2).

Book Scientific Style and Format

Download or read book Scientific Style and Format written by CBE Style Manual Committee and published by Cambridge University Press. This book was released on 1994-11-25 with total page 854 pages. Available in PDF, EPUB and Kindle. Book excerpt: A revised and expanded sixth edition of the "CBE Manual" for scientific authors.

Book A Textbook Of Pharmacovigilance

Download or read book A Textbook Of Pharmacovigilance written by Dr. Kanchana N. Dussa and published by AG PUBLISHING HOUSE (AGPH Books). This book was released on 2023-01-31 with total page 232 pages. Available in PDF, EPUB and Kindle. Book excerpt: Quintessence of Pharmacovigilance refers to the research and practises involved in the identification, evaluation, comprehension, and avoidance of unfavourable effects or the any other potential drug-related issues. The most frequent way to gather safety data is through the spontaneous-reporting of adverse occurrences and adverse medication responses. A substance is equal to a danger when consumed. Consumption of medications is only acceptable when the benefits outweigh the risks. Therefore, the benefit to risk ratio of a medicine determines whether it should be used or not. Due to the individualization of pharmaceuticals for each patient, it is up to the doctor's clinical judgement to choose what will be best for the patient. Observations pertaining to pharmacovigilance can also be used to determine the risk connected to the medicine. Studies on pharmacovigilance provide information on potential dangers connected to a certain medication. Even drugs have the potential to cause unpleasant effects, whether intentional or not. The only scenario in which this generalisation does not apply is when a medication is prescribed because the body lacks certain nutrients, such as certain vitamins or minerals. As the investigation of potential negative effects of medications, this forms the core of pharmacovigilance.

Book Publicaciones de la Organizaci  n Mundial de la Salud

Download or read book Publicaciones de la Organizaci n Mundial de la Salud written by World Health Organization and published by . This book was released on 1978 with total page 464 pages. Available in PDF, EPUB and Kindle. Book excerpt: Vols. for 1973-1977- include publications issued by various WHO regional offices and by the International Agency for Research on Cancer.

Book Quality Control Methods for Medicinal Plant Materials

Download or read book Quality Control Methods for Medicinal Plant Materials written by World Health Organization and published by World Health Organization. This book was released on 1998 with total page 122 pages. Available in PDF, EPUB and Kindle. Book excerpt: A collection of test procedures for assessing the identity, purity, and content of medicinal plant materials, including determination of pesticide residues, arsenic and heavy metals. Intended to assist national laboratories engaged in drug quality control, the manual responds to the growing use of medicinal plants, the special quality problems they pose, and the corresponding need for international guidance on reliable methods for quality control. Recommended procedures - whether involving visual inspection or the use of thin-layer chromatography for the qualitative determination of impurities - should also prove useful to the pharmaceutical industry and pharmacists working with these materials.