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Rules and Guidance for Pharmaceutical Distributors (Green Guide) 2015

distribution practice and wholesale distribution along with relevant information on EU and UK legislation. It brings together the main pharmaceutical;

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Rules and Guidance for Pharmaceutical Distributors (Green Guide)

practice and wholesale distribution along with relevant information on EU and UK legislation. It brings together the main pharmaceutical;

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Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Orange Guide) 2014

of medicines in or for Europe. It is compiled by the UK drug regulatory body, the MHRA, and brings together the European and UK guidance documents and;

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Medicaid Prescription Drugs

manufacturers' lowest or best price. States then share the rebate they receive from pharmaceutical manufacturers with the federal government. This book;

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How to Break Into Pharmaceutical Sales

than one hundred of the country’s top pharmaceutical companies.;

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Patent Regulations and Its Impact on Indian Pharmaceutical Industry

International Product Patent regulations (TRIPS-2005) brings many structural changes in the Indian pharmaceutical sector, which has the;

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How to Sell Validatable Equipment to Pharmaceutical Manufacturers

of discussion include: o Validation and GMP issues o Why validation is so important to pharmaceutical manufacturers o The role of equipment;

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Validating Corporate Computer Systems

One of the biggest computer validation challenges facing pharmaceutical manufacturers is the large corporate system. This book provides;

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Validating Corporate Computer Systems

One of the biggest computer validation challenges facing pharmaceutical manufacturers is the large corporate system. This book provides;

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Generic Drug Product Development

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;

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Surgeons, Manufacturers And Patients

in the very different health economies of the UK and the US.;

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Freeze Drying of Pharmaceutical Products

Freeze Drying of Pharmaceutical Products provides an overview of the most recent and cutting-edge developments and technologies in the;

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Good Manufacturing Practices for Pharmaceuticals

fast pace, pharmaceutical manufacturers, suppliers, contractors, and distributors are impacted by continual change. Offering a wide assortment;

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High Performance Liquid Chromatography

Laboratories where modern HPLC is utilized. Following a hands-on approach, the book gives key insights into the pharmaceutical applications of HPLC and;

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Generic Drug Product Development

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;

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Active Pharmaceutical Ingredients

governmental regulations. Active Pharmaceutical Ingredients is an unparalleled guide to the development, manufacturing, and regulation of the;

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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products is an authoritative and;

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Applications of Ion Chromatography in the Analysis of Pharmaceutical and Biological Products

This is a comprehensive source of information on the application of ion chromatography (IC) in the analysis of pharmaceutical drugs and;

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Drug Delivery Devices and Therapeutic Systems

Drug Delivery Devices and Therapeutic Systems examines the current technology and innovations moving drug delivery systems (DDS;

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Threats and Opportunities for European Pharmaceutical Wholesalers in a Changing Healthcare Environment

opportunities confronting pharmaceutical full-line wholesalers. These businesses are the most important link between pharmaceutical manufacturing and;

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Manufacturing of Pharmaceutical Proteins: From Technology to Economy

resource, this book extensively explores the impact of digital transformation on pharmaceutical protein manufacturers and includes a brand-new;

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British Pharmacopoeia

The "British Pharmacopoeia 2012" is the official collection of standards for UK medicinal products and pharmaceutical substances. It;

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Pharmaceutical Drug Product Development and Process Optimization

pharmaceutical scientists. This volume addresses this challenge by using the Quality by Design (QbD) concept, which was instituted to focus on the;

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Diffusion of the Quality Systems Innovation

Over the past few decades, the FDA has mandated the need for quality systems (QS) for manufacturers of medical device, pharmaceutical and;

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