Event Detail
Good Clinical Practices for the Clinical Research Professional - 4 Part On-line Training Series (Part 1)
July 9 - 23, 2009
- Online Web Seminar / Webinar PA UNITED STATES
DIA
Overview Gain the knowledge required to conduct clinical trials, including knowledge about subject safety, regulations, and the practicalities of performing research studies. What You Will Learn * Roles and responsibilities of each member of the study team * Regulations and guidelines that govern clinical investigations * Consent elements and consent process * Successful patient recruitment and retention strategies * Importance of study compliance during clinical trials * Preparing for audits and audit process