E-BOOK
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E-BOOK
3
Contents
Chapter 1: Navigating complexities in early oncology clinical trials
CHAPTER 1: NAVIGATING COMPLEXITIES IN EARLY ONCOLOGY CLINICAL TRIALS
CHAPTER 2: THE CRUCIAL ROLE OF KIT DESIGN IN SAMPLE COLLECTION
MAXIM #1 STUDY DESIGN
CHAPTER 3: THE CENTRAL LABORATORY’S CRUCIAL ROLE IN STUDY SITE SUPPORT
CHAPTER 4: THE BENEFITS OF CENTRALIZED SAMPLE MANAGEMENT
CHAPTER 5: THE CRUCIAL ROLE OF DATA MANAGEMENT
In the ever-evolving field of oncology, clinical trial play a pivotal role in advancing our understanding of cancer and developing novel treatments. Two prominent trends have emerged in recent years: the first, the increasing development of cancer-targeting drugs, leading to more early-phase clinical trials in oncology; and the second, the growing inclusion of biomarkers in oncology trials.
While these trends hold great promise for personalized cancer treatments, they also present unique challenges. In this article, we will dive into the complexities of early oncology clinical trials, with a specific focus on sample management. We will also explore strategies to effectively address these challenges.
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