Understanding Pharmaceutical Standards and Regulations: Insights Towards Best Practice
Editat de Navneet Sharma, Vikesh Kumar Shukla, Sandeep Aroraen Limba Engleză Hardback – 24 iun 2025
| Toate formatele și edițiile | Preț | Express |
|---|---|---|
| Paperback (1) | 478.82 lei 6-8 săpt. | +24.24 lei 7-13 zile |
| Taylor & Francis – 24 iun 2025 | 478.82 lei 6-8 săpt. | +24.24 lei 7-13 zile |
| Hardback (1) | 1198.09 lei 6-8 săpt. | |
| Taylor & Francis – 24 iun 2025 | 1198.09 lei 6-8 săpt. |
Preț: 1198.09 lei
Preț vechi: 1461.08 lei
-18%
Puncte Express: 1797
Preț estimativ în valută:
211.91€ • 251.71$ • 184.54£
211.91€ • 251.71$ • 184.54£
Carte tipărită la comandă
Livrare economică 28 martie-11 aprilie
Specificații
ISBN-13: 9781032817040
ISBN-10: 1032817046
Pagini: 306
Ilustrații: 58
Dimensiuni: 152 x 229 mm
Greutate: 0.58 kg
Ediția:1
Editura: Taylor & Francis
Colecția Routledge
Locul publicării:Oxford, United Kingdom
ISBN-10: 1032817046
Pagini: 306
Ilustrații: 58
Dimensiuni: 152 x 229 mm
Greutate: 0.58 kg
Ediția:1
Editura: Taylor & Francis
Colecția Routledge
Locul publicării:Oxford, United Kingdom
V-ar putea interesa
-
-23%Preț: 572.19 lei743.11 lei -
Principles and Practice of Clinical ResearchJohn I. Gallin-9%Preț: 602.67 lei662.28 lei -
Pharmaceutical MedicinePhil Ambery-5%Preț: 317.53 lei334.24 lei -
Mosby's Pharmacy Technician: Principles and PracticeElsevier Inc-5%Preț: 806.40 lei848.85 lei -
Aulton's Pharmaceutics: The Design and Manufacture of MedicinesKevin M. G. Taylor-28%Preț: 391.29 lei540.38 lei -
Rules and Guidance for Pharmaceutical Manufacturers and Distributors (Orange Guide) 2022Medicines and Healthcare Products Regulatory Agency-9%Preț: 636.30 lei699.12 lei -
Rules and Guidance for Pharmaceutical Distributors (Green Guide) 2022Medicines and Healthcare Products Regulatory Agency-10%Preț: 539.53 lei601.94 lei -
Preț: 401.90 lei -
Pharmaceutical Process Scale-UpMichael LevinPreț: 408.26 lei -
Manufacturing Process Validation: Concepts, Tools, and Industrial ApplicationsArturo Realyvásquez-Vargas-15%Preț: 415.83 lei489.21 lei -
Pharmaceutical ExcipientsOtilia M y Koo-23%Preț: 1033.51 lei1342.22 lei -
Transforming the Pharmaceutical Supply ChainHedley Rees-19%Preț: 566.64 lei699.56 lei -
Introduction to the Pharmaceutical Sciences: An Integrated ApproachNita K. Pandit PhD-23%Preț: 544.99 lei703.61 lei -
DoctoredCharles PillerPreț: 105.32 lei -
-9%Preț: 24213.42 lei26608.15 lei -
-22%Preț: 548.85 lei700.83 lei -
Practical PharmaceuticsPaul Le Brun-5%Preț: 968.23 lei1019.19 lei -
Medical Product Regulatory AffairsJohn J. Tobin-5%Preț: 639.69 lei673.36 lei -
Method Validation in Pharmaceutical AnalysisJoachim Ermer-5%Preț: 1106.08 lei1164.30 lei -
-23%Preț: 824.65 lei1070.98 lei
Public țintă
Postgraduate and Professional ReferenceCuprins
1. US Pharma Manufacturing Standards: Cfr 210 & 211
2. A Comprehensive Review on the Good Manufacturing Practices Standards: Directive 91/356 of the European Commission
3. Integration Of Cgmp & Gamp-5 In Pharmaceutical Manufacturing
4. Medical Device and Ivds Global Harmonization Task Force Guidance Documents
5. Current Scenario and Future Perspective of Good Laboratory Practices
6. Advancing Laboratory Excellence: A Comprehensive Review of Quality Audits
7. Introduction of Good Automated Laboratory Practices (Galp): Principles and Comparative Analysis Across Regulatory Authorities - Usfda, Ema, Cdsco, And Tga
8. A Framework to Understanding E-Records Under 21cfr Part 11
9. Current Trends in Good Distribution Practices (Gdp)
10. Navigating The Pharmaceutical Supply Chain: Ensuring Integrity Amidst Challenges
11. Optimizing Pharmaceutical Quality: Exploring Out of Specification, Total Quality Management, Change Control
12. Insights Into the Six Sigma Concept
13. Good Regulatory Practices and Validation Plans in Pharmaceutical Practices
14. Critical Utility Validation: An Innovative Approach to Pharmaceutical Best Practices
15. International Council of Harmonization: Reception to Implementation
16. ISO-13485 and Schedule MIII – Quality Management System
2. A Comprehensive Review on the Good Manufacturing Practices Standards: Directive 91/356 of the European Commission
3. Integration Of Cgmp & Gamp-5 In Pharmaceutical Manufacturing
4. Medical Device and Ivds Global Harmonization Task Force Guidance Documents
5. Current Scenario and Future Perspective of Good Laboratory Practices
6. Advancing Laboratory Excellence: A Comprehensive Review of Quality Audits
7. Introduction of Good Automated Laboratory Practices (Galp): Principles and Comparative Analysis Across Regulatory Authorities - Usfda, Ema, Cdsco, And Tga
8. A Framework to Understanding E-Records Under 21cfr Part 11
9. Current Trends in Good Distribution Practices (Gdp)
10. Navigating The Pharmaceutical Supply Chain: Ensuring Integrity Amidst Challenges
11. Optimizing Pharmaceutical Quality: Exploring Out of Specification, Total Quality Management, Change Control
12. Insights Into the Six Sigma Concept
13. Good Regulatory Practices and Validation Plans in Pharmaceutical Practices
14. Critical Utility Validation: An Innovative Approach to Pharmaceutical Best Practices
15. International Council of Harmonization: Reception to Implementation
16. ISO-13485 and Schedule MIII – Quality Management System
Notă biografică
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.
Sandeep Arora, PhD, is a Professor and Director at the 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.
Sandeep Arora, PhD, is a Professor and Director at the Amity Institute of Pharmacy, Amity University, India.
Descriere
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.