Clinical Trial Monitoring: A Sponsor Responsibility 2017 is a webinar that covers topics such as:
- Why Monitor Clinical Studies
- The Sponsor`s responsibility in ensuring quality monitoring
- How does a Sponsor or Site prepare for an Audit?
- What does a Monitor look for?
- The importance of Protocol knowledge in preventing errors
- To understand the importance of a well written Clinical Trial Protocol
- What are the main strategies to improve an audit outcome?
- What are the top 6 GCP problems found by monitors?
- What types of studies are targeted for auditing?
- What does the FDA look at when Auditing/Inspecting a study?
- The Sponsors role in preparing a site for an audit
Clinical Trial Monitoring: A Sponsor Responsibility 2017 is intended for:
- Sponsors and Principal Investigators
- Drug Development Staff
- Study Coordinators
- Clinical Research Associates
- Industry Study Sponsors of Pharmaceutical Products (Drug or Device) Research involving Human Subjects
- Project Managers at CROs
