interpharm press (40 risultati)

Condizione: Good. Boards have some fading to the spine. Content is clean and bright. No DJ.

Condizione: Good. Your purchase helps support Sri Lankan Children's Charity 'The Rainbow Centre'. Ex-library, so some stamps and wear, but in good overall condition. Our donations to The Rainbow Centre have helped provide an education and a safe haven to hundreds of children who live in appalling conditions.

hardcover. Condizione: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!

hardcover. Condizione: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!

hardcover. Condizione: Good. This is a used book in good condition and may show some signs of use or wear . This is a used book in good condition and may show some signs of use or wear .

Condizione: very_good. Supports Goodwill of Silicon Valley job training programs. The cover and pages are in very good condition! The cover and any other included accessories are also in very good condition showing some minor use. The spine is straight, there are no rips tears or creases on the cover or the pages.

Condizione: Good. Light wear to boards. Content is clean with light age tone. DJ with some edge wear and fading.

Condizione: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. Clean from markings In good all round condition. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,1400grams, ISBN:1574911171.

Hardcover. Condizione: Very Good. No Jacket. First Edition. 135 pages. Very good hardback. No inscriptions. --- General information: please email for any more information or condition photos. There may be other minor faults not included here, but this description should include all important points and convey accurately the overall conditon of the book(s). We are happy to give a more detailed description (by volume where applicable) on request. Posted next day (Mon-Fri) from the UK. We normally post by Royal Mail 1st class within the UK, but may use a slower service for books over 1kg or multiple orders or a tracked service for higher value orders. We normally post by Royal Mail Airmail for overseas deliveries, and may request additional postage (at cost) for heavier books or for tracking (buyers always have the option to cancel the order if we do so).

paperback. Condizione: Gut. BUECHERREIEXEMPLAR !!!!Das Buch befindet sich in einem dem Alter endsprechendem guten , gelesenen Zustand.Die Seiten und der Einband sind intakt.BuchrueckenEckenKanten koennen leichte Gebrauchsspuren aufweisen.DIESES BUCH KANN EINEN ODER MEHRERE DER NACHFOLGENDEN MAENGEL AUFWEISEN:NameWidmung im Einband oder auf der ersten Seite, Namens-Etikett auf dem Buchcover, Bücherreiexemplar, Buechereiaufkleber am Buch, sowie Buecherei- oder Schulstempel auf der ersten Seite, Textmarkierungen Sprache: Englisch Gewicht in Gramm: 969.

Condizione: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,850grams, ISBN:0935184163.

Paperback. Condizione: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!

Ring Binder. Condizione: Near Fine. 0935184171. This volume was compiled to collate all applicable regulations concerning Good Manufacturing Practices in the Pharmaceutical Industry. Michael Anisfield has established and directed quality control, quality assurance, production and materials management functions in the industry as well as directing product development acitivities. He has instituted innovative, cost-effective auditing programs for his clients, ensuring that they pass regulatory inspections first time. He is an acclaimed international lecturer on the subject of GMP and Quality topics. The book consists of three parts and an appendix: Part 1: Summary of world-wide requirements and listing of countries with routine overseas inspection programmes. Part 2 : Texts of international GMP requirements. Part 3 : Texts of national GMP requirements. Appendix : Listing of national regulatory agencies responsible for the regulation of drug manufacture. Contents as new. Book.

StapleBound. Condizione: Used, like new. Softcover, staplebound, Revised American Edition, 2002, 75pp. Perfect condition. ** We are a small family business selling fine new and pre-owned books online since 1999, providing professional service and individual attention to your order, daily shipments and sturdy packaging.

Paperback. Condizione: Near Fine. Softcover, ex. library. 92 pages. The Biotechnology Science Coordinating Committee's (BSCC's) definitions for an "integeneric organism (new organism)" and for "pathogen." These definitions are critical to the coordinated framework for the regulation of biotechnology because they establish the types of the organisms subject to certain kinds of review. Contents : I. Preamble; A. Introduction; B. The Coordinated Framework for the Regulation of Biotechnology; C. Interagency Coordination Mechanisms; D. BSCC Definitions; E. International Aspects; II. Statements of Policy; A. Food and Drug Administration; B. Environmental Protection Agency; C. U.S. Department of Agriculture; D. Occupational Safety and Health Administration; E. National Institutes of Health. This notice describes the comprehensive federal regulatory policy for ensuring the safety of biotechnology research and products. The federal agencies needed to have an interagency mechanism for sharing scientific information related to biotechnology, particularly information on research and product applications submitted to the agencies. The Coordinated Framework is based upon health and safety laws developed to address specific product classes. The U.S. Government has written new regulations, policies and guidance to implement these laws for biotechnology as products developed. This framework builds on agency experience with organisms and products developed using conventional techniques, distinguishing between those organisms that require a certain level of federal review and those that do not. A key principle is that genetically engineered organisms would continue to be regulated according to their characteristics and unique features, and not according to their method of production. In other words, for example, if a food product produced through biotechnology is substantially the same as one produced by more conventional means, that food is subject to no additional (or no different) regulatory processes. The framework also maintains that new biotechnology products are regulated under existing federal statutory authorities and regulation. The U.S. policy framework contrasts with that of some of its major trading partners: the European Union, Japan, South Korea, China, Australia and New Zealand who all have separate mandatory labeling requirements for products containing genetically modified organisms. Contents clean, tight and bright. Book.

Hardcover. Condizione: Fine. No Jacket. 7th. 430pp.incl.index; HB burgundy w/white; fine condition w/clean,tight pgs. " .the theory and practical implementation of aseptic (sterile) product manufacturing concepts." illus.

Hardcover. Condizione: Near Fine. 1st Edition. First Edition (Number Line to 1). You can see the covers of the book in the photographs provided. They are very clean. They have very little wear, a tiny tear at the top of the spine, a little crinkling at the bottom of the spine. That's it. This book is very solidly bound. The interior of the book look perfect. The pages are exceptionally clean. I didn't see any soiling. I didn't see any creasing or dogeared corners. There aren't any markings or attachments. And no one has written their name or anything else anywhere in the book. If you're looking for an imperfection, there are a dozen or so pinprick sized spots of dust soiling on the top page edge. They have absolutely no impact on the actual pages.

Hardcover. Condizione: Très bon. Couverture différente. Edition 1994. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Different cover. Edition 1994. Ammareal gives back up to 15% of this item's net price to charity organizations.

Hardcover. Condizione: Used, like new. Like new. Large hardcover with glossy white covers and blue spine, 1993, published by Interpharm Press, 413pp. ISBN = 0935184430. Perfect condition. **OVERSIZE - overseas orders may require additional shipping. **We are a small family business with over 25 years experience providing fine new and pre-owned books online. You can expect professional service and individual attention to your order, daily shipments, and sturdy packaging.

Condizione: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Hardcover. Condizione: Very Good. 1st Edition. Hardcover, xxi + 370 pages, NOT ex-library. Clean and bright throughout with unmarked text, free of inscriptions and stamps, firmly bound. Boards show gentle handling wear, creases along the spine. Published without a dust jacket. -- When a pharmaceutical company decides to build a Quality System, it has to face the fact that there aren't any guideline that define exactly how such a system has to be built. With terms such as quality system, quality assurance, and quality management used interchangeably, even defining the system's objectives is a problem. This book provides a practical guide to building a quality system. Beginning with explanations of key terms and concepts, it covers ISO 9000 and GMP and how to combine them, and includes a matrix showing their similarities and differences. Implementation reviews illustrate how Quality (Management) Systems have been installed successfully in pharmaceutical companies. Also covered are the individual components of a Quality System; auditing, validation, and supplier qualification systems; and Hazard Analysis Critical Control Points (HACCP). -- Contents: Introduction in Quality Systems [What Is Quality?; What Is Quality Assurance (QA)?; What Is Quality Management?; What Is a Quality System? Documented Quality System]; Experiences in the Inspecting of Quality Systems: An Inspector's View [Regulatory Requirements; Management Representative or QA Department?; Forms of Organisation; Difference Between the United States and Europe; Evaluation of Quality Systems by the Supervisory Authority]; GMP/ISO Quality Systems for Drug Products Manufacturers [ISO 9000: A Critical Assessment; How the ISO 9000 Series Came About; Objectives of ISO 9000; Content of ISO 9000-1; Outlook: Revision of ISO 9000; What Are the Consequences of the Revision?]; Quality Management Systems and GMP [Characteristics of a Quality Management System; Correlation of GMP and ISO; Rationale; Performance Measurements; Benefits; Certification; Conclusion; Matrix]; Master Plan Concept: GMP-Compliant Production in a Non-GMP Environment [Current Situation; Integrating GMP into ISO 9001; Quality System without ISO 9001: The Master Plan Concept; Applications]; A Quality Manual for a Multinational Pharmaceutical Company [Background; How Is a Quality Manual Developed?; Scope; Hierarchy; Process to Generate Standards; Standards Content; Implementation Strategy; Availability; Value Added]; Implementation of a Quality Assurance System into a German Pharmaceutical Company [QA System: A Current Viewpoint on National and International Laws and Regulations; Definition of the Term Quality Assurance System; Three Columns of a QA System; Support of the Three Columns by Defined Responsibilities According to German Law; Building Up of New Specific Systems; Task of the Person in Charge of QA; Building up a QA System; Implementation of a QA System; Extension of the QA System; Implementation of some Relevant Items of the DIN EN ISO Standards; Structure and Responsibility of the QA Department at Biotest AG]; Implementation of a Quality System: A Report of Practical Experience [Project Description; Expansion of the Quality System]; Experiences in the Auditing of Quality Assurance Systems: Industry's View [Quality Management: Implications for the Pharmaceutical Industry]; How to Implement Validation into a QA System [Validation Activities; Scope of Validation; Basic Validation Concept; Strategy for the Implementation of Validation into a QA System; Validation Master Plan Concept; Outline of a VMP for a Pharmaceutical Production Plant; Benefits of Validation]; How to Build a Supplier Qualification System [Qualification of Suppliers; Qualification Concept]; Hazard Analysis and Critical Control Points in a Pharmaceutical QA System [HACCP Concept; Example of HACCP Analysis; Product Validation Plan (PVP)]; Summary; References.

Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.

Condizione: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.

Hardcover. Condizione: Very Good. The book has slight edge wear, dirt smudging on the text block and back cover, and rubbing on covers.otherwise it is crisp, unmarked, and tightly bound.

Hardcover. Condizione: Very Good. Hardcover (no dust jacket; printed boards). Very good condition. No notable flaws. Pages are sound and clear. TA. Used.

Hardcover. Condizione: Used - Very Good. No Jacket. Large hardcover with white glossy illustrated covers. No marks or signs of being used. 11.25 x 9.75 with 801 pp including index. Illustrated with color photographs. Owners name on ffep. 6 pounds.

Condizione: As New. Unread book in perfect condition.

Condizione: New.

Condizione: As New. Unread book in perfect condition.