Texas Zurcher

Social Media as Recruitment Tool

Chapter 1 Lecture 7 Spelling Rules

Chapter 5 Lecture 3 Health & Wellness

Safety Reporting

Adverse Events

Conflicts of Interest

Protocol Deviations

Protocol Amendments

FDA Form 1572

Clinical Trial Monitoring

21 CFR Part 11

FDA Audits

Sponsor Audits

Serious Adverse Events

Adverse Events

Investigator and Site Qualifications

Study Participants Retention

Study Participants Recruitment

Informed Consent

Study Closure

Study Initiation Sponsor Relationships

Study Initiation Regulatory Files

Study Initiation Feasibility and Budgeting

HIPAA

Source Documentation and Case Report Forms

SOPs

Patient Recruitment

Institutional Review Boards 1

The Study Protocol

Informed Consent