Guide to ensure accuracy and safety in your clinical trials with vigilant equipment management, all documented for ready verification and adherence to protocol standards
Archives: Offerings
A process for the preparation, review, implementation and retirement of an SPG
Traceable Case Report Forms crafted to connect each data point back to its origin, ensuring data integrity
A guide for diligent management of IRB applications and reporting obligations through meticulous documentation and tracking of responsibilities
A course introducing the regulatory responsibilities of sponsors and investigators in drug and device studies
A guide to tailor internal audits to the study’s context and history, documenting all resolutions for continuous improvement and adherence to ethical, safe, and high-quality research protocols
Seminar series on research ethics and integrity, with interactive sessions and documentation for NIH training requirements
Guide to implementing a structured RCR training program with materials available for download to meet NIH face-to-face RCR education requirements
Study-specific, local, and federal guidelines for AEs, SAEs, UADEs, and Unanticipated Problems to maintain regulatory congruence and integrity in research practice
Ten-week full-time research experience in translational science and health disparities, including mentorship, training, and hands-on projects, with paid positions for students