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- Budget Tool Helps Investigative Sites Calculate the Cost of a Coordinator’s Time for a Typical Outpatient Study Visit Part I
- Budget Tool Helps Investigative Sites Calculate the Cost of a Coordinator’s Time for a Typical Outpatient Study Visit - Part II
- The Role of Data Monitoring Committees and their Impact on Clinical Research Associate Responsibilities
- Recruitment and Retention of Patients and Site Management
- Psychodynamic Influences on Human Subject Recruiting Practices
- Informed Consent or Intuitive Consent?
- Culturally Competent Consent Concepts
- "…in language understandable to the subject…"--or not.
- What Does it take to Remember Informed Consent?
- Risk Overload and Risk Misdirection in the Consent Process
- Why You Shouldn’t Test for Consent Comprehension
- Readability Recommendations: Easier Said Than Done
- Lay Lab Language for Informed Consents
- The HIPAA Privacy Rule and Research
- ERES Compliance and Data Integrity Issues in e-Trials
- Setting Up a Clinical Research Program in the Community Hospital Setting
- END OF LIFE ISSUES IN CLINICAL RESEARCH
- Budget Tool Helps Investigative Sites Calculate the Cost of a Coordinator’s Time for a Typical Outpatient Study Visit Part I
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- Advanced Site Management: Finance and Productivity Enhanced Business Practices for Clinical Research Programs
- Harnessing Social Media to Advance Clinical Research
- Protecting Human Research Participants: Legal, Ethical, and Practical Considerations
- Clinical Investigator GCP & Trials Management Program for Clinical Investigators and Key Research Staff
- Clinical Research Monitoring and GCP Workshop for Monitors, Site Coordinators and Auditors
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- Bedside Nursing "From Clinical Inquiry to Conducting Nursing Research"
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