Clinical Compliance 2011 - Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Date2011-02-10
Deadline2011-02-10
VenuePalo Alto, USA - United States
KeywordsClinical Webinar ,conference,event,Webinar
Topics/Call fo Papers
Areas Covered in this Webinar:
Key aspects of the role and key players involved in a trial.
Understanding compliance.
Most frequent audit findings.
Audit preparation.
Activities that are common to audits.
Linking responsibility to these activities.
Responding to audit findings.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:
Clinical trial sponsors study team
CROs study team
Study managers, Clinical team leads, CRAs
Principal investigators, site managers and study coordinators
Regulatory Compliance Associates and Managers
Key aspects of the role and key players involved in a trial.
Understanding compliance.
Most frequent audit findings.
Audit preparation.
Activities that are common to audits.
Linking responsibility to these activities.
Responding to audit findings.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in:
Clinical trial sponsors study team
CROs study team
Study managers, Clinical team leads, CRAs
Principal investigators, site managers and study coordinators
Regulatory Compliance Associates and Managers
Other CFPs
- Trial Master File for Research Sites: Can You Pass FDA Inspection? - Webinar By ComplianceOnline
- How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
- Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements
- Eliminate the Confusion ?Annex 13 GMP guide - Webinar By ComplianceOnline
- 3 hr Webinar on - Garnishments: Complete and In-Depth - Webinar By ComplianceOnline
Last modified: 2010-12-23 19:36:56