Research Sponsors

CenterWatch | Insights

People, Process and Technology: The Right Combination for Successful Expert Committees

CenterWatch | Insights

Ellyn Getz: Communicating the Value of Clinical Trials to Underserved Minority Communities

CenterWatch | Insights

PART 12: Public Awareness of Clinical Research and the Path To Diversity in Clinical Trials

CenterWatch | Insights

What are the regulations for training home health individuals who are working remotely to collect study data?

CenterWatch | Insights

Part 4: Planning for Recovery: How Research Sponsors and Research Sites are Thinking Ahead to Restart Research

CenterWatch | Insights

Part 3: Evaluating Study Status and Leveraging Data Monitoring Committees to Make Study Decisions

CenterWatch | Insights

Remote Clinical Research Coordinator Service

CenterWatch | Insights

What are the requirements for parental permission (consent) in studies involving children?

CenterWatch | Insights

How do I handle a deviation in the use of blood specimens collected outside the timeframe?

CenterWatch | Insights

Is it possible to make a PI’s name or institution confidential on a consent form?