Compliance Notices (from 14-001 to 23-XXX)
Standard Rates for Ancillary and Inpatient Clinical Research Services
Good Clinical Practice Training Requirement
Industry-sponsored Clinical Research Withholding Requirements
Industry-Sponsored and Investigator-Initiated Clinical Trial/Research Facilities
Material Transfer and Data Use Agreement Procedures
Full Cost Recovery Guidelines for Clinical Research
Use of Accelerated Confidentiality Disclosure Agreement Template
Agreement Review, Negotiation, Acceptance, and Notification Compliance Notice
Scheduling Research Participants for VCUHS Services - GE/IDX
OnCore - VCU's Clinical Research Management System Requirements
Clinical Research Coverage Analysis
Compliance Review Fee For Industry Sponsored Studies Reviewed By An External IRB
VCU Oversight of Subrecipients on Sponsored Projects Compliance Notice
Notification Requirement for Research Subject to External Audit or Inspection
ClinicalTrials.gov Registration and Results Reporting
ClinicalTrials.gov Registration and Results Reporting
Sponsored Project and Research Volunteers
Compliance with the Federal Funding Accountability and Transparency Act
Clinical Trial Administration Service Center and Fees
Limited submission opportunities
NIH and NSF Research Fellows and Trainees
Oversight and Management of VCU Core Laboratories
VCU Employee and Facility Use Guidelines for Clinical Research
Overview of human subjects research audits and monitoring conducted by VCU overs
Managing Allegations of Undue Influence in Research Committees and Groups
Cannabis Research, Teaching, and Outreach Activities
Creation of Compliance Notices
Federal notification requirement regarding sexual assault, harassment, bullying,
Posting of Clinical Trial Informed Consent Forms
Standardized Process for VCU Research Payments
PRMC Approval Required for Cancer-Related Research Involving Human Subjects
Award Transfers From Another Institution to VCU
Award Transfers From VCU to Another Institution
Research-related Institutes and Centers
OVPRI Matching Funds Program for Research Equipment
Subject injury language requirement and review for industry-sponsored human subjects research
20-008 Division of Sponsored Programs responsibilities
21-001 Individual development plans for graduate students and postdoctoral researchers
21-002 International shipping of biological materials
23-001 Institutional requirement to use Veeva eTMF for multi-center clinical trials whe
23-002 Institutional requirement to use Veeva SiteVault for clinical trials
24-001 Use of VCU Health Investigational Drug Services for clinical trials