GCP Audit. Part C. GCP审核课程. Data Fabrication and Falsification. Access granted on May 08,2023
审核员GCP
审计员, GCP
审计员, GCP 职责 GCP 审核员负责对受 GCP 约束的所有活动进行质量保证审核, “ICH 良好临床实践: 综合指南,” (地面控制点), 支持质量保证计划 (质量保证) 为了保证 阅读更多…
相关文章
审核员GCP
Senior Clinical Research Associate
Responsibilities Assisting in the design and execution of high quality clinical studies in compliance with FDA and ICH requirements. Function as a primary liaison to clinical investigators/site staff. Identify, qualify, initiate, monitor and close out 阅读更多…
GCP审核
GCP Auditor certification. Stage 2. Part C. Access granted on May 08,2023
GCP Auditor certification. Stage 2. Part C. Access granted on May 08,2023
