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Verlag: Taylor & Francis Ltd, London, 2025
ISBN 10: 1032814128 ISBN 13: 9781032814124
Sprache: Englisch
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Paperback. Zustand: new. Paperback. This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies to navigate the intricacies of different regulatory environments so that pharmaceutical companies can operate internationally, avoiding the potentially costly risk of violations. Detailed and holistic, the book is an essential resource to pharmaceutical researchers and manufacturers, as well as an important resource for students and scholars in the field. This resource provides a guide to the regulations and standards which govern the international pharmaceutical industry. Featuring explanations of regulations and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing and distribution. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Verlag: Taylor and Francis Ltd, GB, 2025
ISBN 10: 1032814128 ISBN 13: 9781032814124
Sprache: Englisch
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Verlag: Taylor & Francis Ltd, London, 2025
ISBN 10: 1032814128 ISBN 13: 9781032814124
Sprache: Englisch
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In den WarenkorbPaperback. Zustand: new. Paperback. This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies to navigate the intricacies of different regulatory environments so that pharmaceutical companies can operate internationally, avoiding the potentially costly risk of violations. Detailed and holistic, the book is an essential resource to pharmaceutical researchers and manufacturers, as well as an important resource for students and scholars in the field. This resource provides a guide to the regulations and standards which govern the international pharmaceutical industry. Featuring explanations of regulations and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing and distribution. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Zustand: New. Navneet Sharma, PhD, is an Assistant Professor at Amity Institute of Pharmacy, Amity University, India.Vikesh Kumar Shukla, PhD, is an Associate Professor and Centre Head at Amity Institute of Pharmacy, Amity University, India.
Verlag: Taylor and Francis Ltd, GB, 2025
ISBN 10: 1032814128 ISBN 13: 9781032814124
Sprache: Englisch
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EUR 87,80
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In den WarenkorbPaperback. Zustand: New. This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies to navigate the intricacies of different regulatory environments so that pharmaceutical companies can operate internationally, avoiding the potentially costly risk of violations. Detailed and holistic, the book is an essential resource to pharmaceutical researchers and manufacturers, as well as an important resource for students and scholars in the field.
Anbieter: preigu, Osnabrück, Deutschland
Taschenbuch. Zustand: Neu. Understanding Pharmaceutical Standards and Regulations | Insights Towards Best Practice | Navneet Sharma (u. a.) | Taschenbuch | Einband - flex.(Paperback) | Englisch | 2025 | Routledge | EAN 9781032814124 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu.
Anbieter: GreatBookPricesUK, Woodford Green, Vereinigtes Königreich
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Verlag: Taylor & Francis Ltd, London, 2025
ISBN 10: 1032817046 ISBN 13: 9781032817040
Sprache: Englisch
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Hardcover. Zustand: new. Hardcover. This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies to navigate the intricacies of different regulatory environments so that pharmaceutical companies can operate internationally, avoiding the potentially costly risk of violations. Detailed and holistic, the book is an essential resource to pharmaceutical researchers and manufacturers, as well as an important resource for students and scholars in the field. This resource provides a guide to the regulations and standards which govern the international pharmaceutical industry. Featuring explanations of regulations and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing and distribution. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Verlag: Taylor & Francis Ltd, London, 2025
ISBN 10: 1032817046 ISBN 13: 9781032817040
Sprache: Englisch
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In den WarenkorbHardcover. Zustand: new. Hardcover. This unique resource provides a comprehensive guide to the evolving regulations and standards which govern the international pharmaceutical industry. Featuring clear explanations of the latest regulations, as well as insights and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing, and distribution. It also offers strategies to navigate the intricacies of different regulatory environments so that pharmaceutical companies can operate internationally, avoiding the potentially costly risk of violations. Detailed and holistic, the book is an essential resource to pharmaceutical researchers and manufacturers, as well as an important resource for students and scholars in the field. This resource provides a guide to the regulations and standards which govern the international pharmaceutical industry. Featuring explanations of regulations and strategies to maintain compliance, the book covers the key principles of best-practice for laboratory research, manufacturing and distribution. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.