東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

FindBook

Google Book

Amazon

博客來

Fundamentals of decentralized clinical trials = strategy and execution /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Fundamentals of decentralized clinical trials/ edited by Anna H. Yang, Isaac R. Rodriguez-Chavez.
其他題名:	strategy and execution /
其他作者:	Yang, Anna H.
出版者:	Cham :Springer International Publishing : : 2024.,
面頁冊數:	xvii, 83 p. :ill., digital ;24 cm.
內容註:	1. INTRODUCTION AND OVERVIEW OF DECENTRALIZED CLINICAL TRIALS -- 2. TECHNOLOGY LANDSCAPE AND REQUIREMENTS -- 3. REGULATORY LANDSCAPE -- 4. METHODOLOGY AND PROTOCOL DEVELOPMENT -- 5. GOALS AND METRICS OF SUCCESS.
Contained By:	Springer Nature eBook
標題:	Clinical trials. -
電子資源:	https://doi.org/10.1007/978-3-031-62877-1
ISBN:	9783031628771

Fundamentals of decentralized clinical trials = strategy and execution /
Fundamentals of decentralized clinical trialsstrategy and execution /[electronic resource] :edited by Anna H. Yang, Isaac R. Rodriguez-Chavez. - Cham :Springer International Publishing :2024. - xvii, 83 p. :ill., digital ;24 cm.

1. INTRODUCTION AND OVERVIEW OF DECENTRALIZED CLINICAL TRIALS -- 2. TECHNOLOGY LANDSCAPE AND REQUIREMENTS -- 3. REGULATORY LANDSCAPE -- 4. METHODOLOGY AND PROTOCOL DEVELOPMENT -- 5. GOALS AND METRICS OF SUCCESS.

A timely and first-of-its-kind publication in the field, this short handbook on decentralized clinical trials (DCTs) offers a thorough exploration of the potential of DCTs to revolutionize clinical research through innovative approaches, including technology. This concise and easy-to-read publication is especially designed for those who seek to understand and get up-to-speed on what DCTs mean and how to work in this rapidly evolving field. As discussed in Chapter 1, DCTs address barriers to traditional trial participation, promoting accessibility, diversity, equity, and participant engagement. Chapter 2 examines how the COVID-19 pandemic and evolving regulations accelerated the adoption of DCTs, building on their application since the early 2000s. Chapters 3 and 4 highlight remaining operational complexities and the importance of careful trial design to ensure scientific rigor, operational feasibility, and compliance with regulations, ethics, data privacy, and participant safety. The book emphasizes the significance of the FDA's draft guidance on DCTs, detailing investigator responsibilities, local health care providers' use, and essential sponsor considerations. Chapter 5 stresses the need for clear metrics to evaluate DCT adoption's impact on recruitment, retention, diversity, safety, and cost efficiencies. Overall, this guide tracks DCT advancements and encourages readers to contribute to evidence-based integration, meeting participant expectations for convenience and fostering faster, more inclusive clinical studies. Ultimately, this book aims to support the transformation of modern clinical research, developing medical products more efficiently for those in need. A major contribution to the literature on clinical research, this work will be a resourceful tool to anyone interested in embracing decentralized clinical research and improving access and participation for all.

ISBN: 9783031628771

Standard No.: 10.1007/978-3-031-62877-1doiSubjects--Topical Terms:

724498
Clinical trials.

LC Class. No.: R853.C55

Dewey Class. No.: 615.50724

Fundamentals of decentralized clinical trials = strategy and execution /
LDR:03146nmm a2200325 a 4500 001 2380003
003 DE-He213
005 20241016125726.0
006 m d
007 cr nn 008maaau
008 250418s2024 sz s 0 eng d
020 $a 9783031628771 $q (electronic bk.)
020 $a 9783031628795 $q (paper)
024 7 $a 10.1007/978-3-031-62877-1 $2 doi
035 $a 978-3-031-62877-1
040 $a GP $c GP
041 0 $a eng
050 4 $a R853.C55
072 7 $a MMG $2 bicssc
072 7 $a MED071000 $2 bisacsh
072 7 $a MKG $2 thema
082 0 4 $a 615.50724 $2 23
090 $a R853.C55 $b F981 2024
245 0 0 $a Fundamentals of decentralized clinical trials $h [electronic resource] : $b strategy and execution / $c edited by Anna H. Yang, Isaac R. Rodriguez-Chavez.
260 $a Cham : $b Springer International Publishing : $b Imprint: Springer, $c 2024.
300 $a xvii, 83 p. : $b ill., digital ; $c 24 cm.
505 0 $a 1. INTRODUCTION AND OVERVIEW OF DECENTRALIZED CLINICAL TRIALS -- 2. TECHNOLOGY LANDSCAPE AND REQUIREMENTS -- 3. REGULATORY LANDSCAPE -- 4. METHODOLOGY AND PROTOCOL DEVELOPMENT -- 5. GOALS AND METRICS OF SUCCESS.
520 $a A timely and first-of-its-kind publication in the field, this short handbook on decentralized clinical trials (DCTs) offers a thorough exploration of the potential of DCTs to revolutionize clinical research through innovative approaches, including technology. This concise and easy-to-read publication is especially designed for those who seek to understand and get up-to-speed on what DCTs mean and how to work in this rapidly evolving field. As discussed in Chapter 1, DCTs address barriers to traditional trial participation, promoting accessibility, diversity, equity, and participant engagement. Chapter 2 examines how the COVID-19 pandemic and evolving regulations accelerated the adoption of DCTs, building on their application since the early 2000s. Chapters 3 and 4 highlight remaining operational complexities and the importance of careful trial design to ensure scientific rigor, operational feasibility, and compliance with regulations, ethics, data privacy, and participant safety. The book emphasizes the significance of the FDA's draft guidance on DCTs, detailing investigator responsibilities, local health care providers' use, and essential sponsor considerations. Chapter 5 stresses the need for clear metrics to evaluate DCT adoption's impact on recruitment, retention, diversity, safety, and cost efficiencies. Overall, this guide tracks DCT advancements and encourages readers to contribute to evidence-based integration, meeting participant expectations for convenience and fostering faster, more inclusive clinical studies. Ultimately, this book aims to support the transformation of modern clinical research, developing medical products more efficiently for those in need. A major contribution to the literature on clinical research, this work will be a resourceful tool to anyone interested in embracing decentralized clinical research and improving access and participation for all.
650 0 $a Clinical trials. $3 724498
650 1 4 $a Pharmacology. $3 634543
650 2 4 $a Clinical Research. $3 3531315
650 2 4 $a Biomedical Research. $3 851895
650 2 4 $a Drug Safety and Pharmacovigilance. $3 2108855
650 2 4 $a Therapeutics. $3 680391
700 1 $a Yang, Anna H. $3 3733192
700 1 $a Rodriguez-Chavez, Isaac R. $3 3733193
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer Nature eBook
856 4 0 $u https://doi.org/10.1007/978-3-031-62877-1
950 $a Biomedical and Life Sciences (SpringerNature-11642)