Synopsis
Clinical Research: Principles and Practice is a clear and practical guide to understanding clinical research from core concepts to real-world application. Written for students and professionals, this book explains not only what is done in clinical research, but why each step is essential for patient safety, data integrity, and regulatory compliance.
The content is presented in a logical, step-by-step manner, making complex topics easy to understand and remember. High-quality illustrations and diagrams help simplify trial design, documentation, monitoring, data management, and regulatory processes, allowing readers to grasp concepts quickly and confidently.
The book covers the complete clinical research lifecycle, including trial organization, ethical and regulatory requirements, roles and responsibilities, investigational product management, documentation systems, monitoring, quality assurance, audits, and clinical data management. Strong emphasis is placed on practical understanding alongside academic foundations.
Who This Book Is For
M.Pharm (Pharmacology), Pharm.D, and B.Pharm students preparing for university exams, viva voce, and competitive assessments
Medical students and clinicians seeking a clear understanding of clinical trial processes and regulatory responsibilities
Pharmaceutical industry professionals working in clinical research, regulatory affairs, pharmacovigilance, and quality assurance
CRO professionals, study coordinators, and monitors
"synopsis" may belong to another edition of this title.
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CLINICAL RESEARCH: Principles and Practice
Seller: California Books, Miami, FL, U.S.A.
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Clinical Research
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PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. Seller Inventory # L0-9798903191154
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Clinical Research
Print on DemandSeller: PBShop.store UK, Fairford, GLOS, United Kingdom
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Clinical Research (Paperback)
Print on DemandSeller: Grand Eagle Retail, Bensenville, IL, U.S.A.
Seller rating 5 out of 5 stars
Paperback. Condition: new. Paperback. Clinical Research: Principles and Practice is a clear and practical guide to understanding clinical research from core concepts to real-world application. Written for students and professionals, this book explains not only what is done in clinical research, but why each step is essential for patient safety, data integrity, and regulatory compliance.The content is presented in a logical, step-by-step manner, making complex topics easy to understand and remember. High-quality illustrations and diagrams help simplify trial design, documentation, monitoring, data management, and regulatory processes, allowing readers to grasp concepts quickly and confidently.The book covers the complete clinical research lifecycle, including trial organization, ethical and regulatory requirements, roles and responsibilities, investigational product management, documentation systems, monitoring, quality assurance, audits, and clinical data management. Strong emphasis is placed on practical understanding alongside academic foundations.Who This Book Is ForM.Pharm (Pharmacology), Pharm.D, and B.Pharm students preparing for university exams, viva voce, and competitive assessmentsMedical students and clinicians seeking a clear understanding of clinical trial processes and regulatory responsibilitiesPharmaceutical industry professionals working in clinical research, regulatory affairs, pharmacovigilance, and quality assuranceCRO professionals, study coordinators, and monitors This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Seller Inventory # 9798903191154
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Clinical Research (Paperback)
Print on DemandSeller: CitiRetail, Stevenage, United Kingdom
Seller rating 5 out of 5 stars
Paperback. Condition: new. Paperback. Clinical Research: Principles and Practice is a clear and practical guide to understanding clinical research from core concepts to real-world application. Written for students and professionals, this book explains not only what is done in clinical research, but why each step is essential for patient safety, data integrity, and regulatory compliance.The content is presented in a logical, step-by-step manner, making complex topics easy to understand and remember. High-quality illustrations and diagrams help simplify trial design, documentation, monitoring, data management, and regulatory processes, allowing readers to grasp concepts quickly and confidently.The book covers the complete clinical research lifecycle, including trial organization, ethical and regulatory requirements, roles and responsibilities, investigational product management, documentation systems, monitoring, quality assurance, audits, and clinical data management. Strong emphasis is placed on practical understanding alongside academic foundations.Who This Book Is ForM.Pharm (Pharmacology), Pharm.D, and B.Pharm students preparing for university exams, viva voce, and competitive assessmentsMedical students and clinicians seeking a clear understanding of clinical trial processes and regulatory responsibilitiesPharmaceutical industry professionals working in clinical research, regulatory affairs, pharmacovigilance, and quality assuranceCRO professionals, study coordinators, and monitors This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Seller Inventory # 9798903191154
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£ 35.49
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Clinical Research (Paperback)
Print on DemandSeller: AussieBookSeller, Truganina, VIC, Australia
Seller rating 5 out of 5 stars
Paperback. Condition: new. Paperback. Clinical Research: Principles and Practice is a clear and practical guide to understanding clinical research from core concepts to real-world application. Written for students and professionals, this book explains not only what is done in clinical research, but why each step is essential for patient safety, data integrity, and regulatory compliance.The content is presented in a logical, step-by-step manner, making complex topics easy to understand and remember. High-quality illustrations and diagrams help simplify trial design, documentation, monitoring, data management, and regulatory processes, allowing readers to grasp concepts quickly and confidently.The book covers the complete clinical research lifecycle, including trial organization, ethical and regulatory requirements, roles and responsibilities, investigational product management, documentation systems, monitoring, quality assurance, audits, and clinical data management. Strong emphasis is placed on practical understanding alongside academic foundations.Who This Book Is ForM.Pharm (Pharmacology), Pharm.D, and B.Pharm students preparing for university exams, viva voce, and competitive assessmentsMedical students and clinicians seeking a clear understanding of clinical trial processes and regulatory responsibilitiesPharmaceutical industry professionals working in clinical research, regulatory affairs, pharmacovigilance, and quality assuranceCRO professionals, study coordinators, and monitors This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability. Seller Inventory # 9798903191154