CenterWatch’s proprietary charts and figures from the 2009 edition of State of the Clinical Trials Industry are now available as convenient, easy-to-integrate PowerPoint slides for use in presentations, business analysis, and market research.
State of the Clinical Trials Industry is a comprehensive resource examining all aspects of the global clinical trials industry and is filled with original CenterWatch data, collected from our global clinical research benchmarking surveys, representing an analysis of current sponsor and CRO practices.
PowerPoint slides are available in seven pre-packaged sets:
CenterWatch Physician Survey on Patient Referrals to Clinical Trials
Number of data slides: 17
(Item #: S09628A)
- An examination of physician attitudes towards clinical trials
- Data gathered from a 2007 survey of 954 randomly selected physicians from the Physicians' Desk Reference (PDR)
- Survey data includes:
- Why physicians become investigators and why they would or would not conduct trials
- Reasons why physicians do not refer patients into trials
- What factors would increase a physician's comfort level with referring patients into clinical trials
- The top therapeutic areas of physician referrals and any special training that physicians have received on conducting trials
CenterWatch Investigative Site Survey Assessing Sponsors and CROs – United States
Number of data slides: 30
(Item #: S09628B)
An examination of the quality of relationships that sponsors and CROs have with their U.S. investigative sites
- Data gathered from a 2007 survey of U.S. investigative sites; 522 surveys completed
- Survey data includes:
- Investigative site ratings of sponsor and CRO companies across specific clinical dimensions including project management, study initiation, ongoing study conduct, and the grant payment process
- Sponsor and CRO rankings based on their scores across survey attributes
- Major factors that cause study delays and length of enrollment delays
CenterWatch Investigative Site Survey Assessing Sponsors and CROs – Europe and Canada
Number of data slides: 28
(Item #: S09628C)
- An examination of the quality of relationships that sponsors and CROs have with their European and Canadian investigative sites
- Data gathered from a 2008 survey of European and Canadian investigative sites; 653 surveys completed
- Survey data includes:
- Investigative site ratings of sponsor and CRO companies across specific clinical dimensions including project management, study initiation, ongoing study conduct, and the grant payment process
- Sponsor and CRO rankings based on their scores across survey attributes
- Major factors that cause study delays and length of enrollment delays
CenterWatch Analysis of Clinicaltrials.gov Trial Listings
Number of data slides: 18
(Item #: S09628D)
- An analysis of trials listed on Clinicaltrials.gov examining the proportion of trials by Phase and country
- Data based on CenterWatch analysis of drug and biological listings on www.clinicaltrials.gov, the NIH trial registry
- Data analysis includes:
- The type of clinical trial sponsor (NIH, government, or industry) and proportion of trials by Phase (I-IV)
- An investigation of industry sponsorship by Phase and country of sponsorship
- NIH sponsorship of trials by Phase and by country of sponsorship
CenterWatch EDC Training and Investigator Meeting Surveys
Number of data slides: 22
(Item #: S09628E)
- Data gathered from two surveys in 2005 and 2007 of more than 100 investigative sites on EDC training and investigator meetings
- Survey data from the Investigator Meeting Survey includes:
- Types of investigator meetings and the learning method that is preferred by survey respondents
- The most valuable aspects of investigator meetings and the advantages of remote meetings
- Survey data from the EDC Training Survey includes:
- The quality and type of training that a site receives on EDC
- Site value-assessment of EDC training and whether EDC training has improved or declined
- Percent of trials that use EDC at a site (on average) and the type of EDC that is being used
1572 Analysis of Investigators
Number of data slides: 25
(Item #: S09628F)
- An investigation of trends over time for the number of trials initiated by investigators
- Data based on CenterWatch analysis of a Bioresearch Monitoring Information Systems (BMIS) data file from the FDA Center for Drug and Evaluation (CDER) containing information extracted from investigators filing FDA 1571 or 1572 form
- Data analysis includes:
- Comparison of investigator participation by country and by geographic region
- Classification of new investigators by country, percentage of first-time investigators, and investigators who participate in one trial
CenterWatch Survey of Study Volunteers
Number of data slides: 32
(Item #: S09628G)
- An examination of the study volunteer's experience of having participated in a clinical trial
- Data gathered from a 2008 survey of 590 study volunteers who have participated in a trial and subscribe to the CenterWatch Patient Notification Service
- Survey data includes:
- How volunteers learn about trials and those factors that influence their decision to participate
- Volunteers’ understanding of study expectations, including aspects of informed consent, and overall volunteer satisfaction with medical care
- Comparison data from past CenterWatch study volunteer surveys
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