Vikesh Kumar Shukla – författare
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4 produkter
4 produkter
Häftad, Engelska, 2025
967 kr
Skickas inom 10-15 vardagar
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.
Inbunden, Engelska, 2025
2 508 kr
Skickas inom 10-15 vardagar
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.
E-bok
PDF, Engelska, 20251 143 kr
Läs direkt efter köp
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.
E-bok
Engelska, 20251 143 kr
Läs direkt efter köp
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.