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Current Collaborative Projects - Enrollment Open
Assessing GLP Compliance and Quality Practices in China
Project Stages
About Collaborative Projects
Current Collaborative Projects - Enrollment Open
Evaluating Preclinical Cardio-Toxicity Assessment Tools
Leveraging Biomarker & Translational Research in China
Assessing GLP Compliance and Quality Practices in China
Exploiting Legacy Safety Studies
Assessing the Asian Supply Chain of Non-Human Primates (NHPs)
Case Studies of Past CHA Projects
Project Stages
STAGE I: Client Driven Project Design
Preliminary draft of study protocols prepared, discussion on study species and test substance(s), preliminary discussion with potential lab partners. Recruitment of clients and test facilities begins.
Timing: April-May 2007
STAGE II: Final Draft of Study Protocols, Implementation Objectives & Kickoff Peer-to-Peer Roundtable
Formal project launches with circulation of revised draft study protocols and overall project objectives. Client-only, peer-to-peer roundtable (conducted via web conference) scheduled to discuss specific issues and build consensus on final project operation plan. Follow-up one-on-one teleconference between each client and CHA project team as appropriate. Protocols sent to test facilities to begin cost negotiations.
Timing: May-June, 2007
STAGE III: Study Execution
Final agreement reached on protocols and with facilities being evaluated. In-life parts of studies initiated. Operational oversight established and process of rapid information/data feedback implemented.
Timing: June-October, 2007
STAGE IV: Mid Study Evaluation & Second Peer-to-Peer Roundtable
Analysis and normalization of information and data collected to date through one-on-one meetings and a second, client-only peer-to-peer roundtable (conducted via web conference). Feedback generated and any midcourse corrections made as necessary.
Timing: August, 2007
STAGE V: Findings Report, Presentation & Third Peer-to-Peer Roundtable
CHA presents a summary of findings and facilitates a peer-to-peer discussion of resulting implications and opportunities (via web conference with clients and facility partners). Final reports distributed to each participating organization.
Timing: November-December 2007
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