A broad overview of human subjects research and best practices that can be adapted to any type of research
Keyword: best practices
Workshop on best practices when preparing for a new study or beginning a new phase of research
An online module rooted in GCP principles on best practices for clinical and translational research
Comprehensive training, organizational contacts, and meticulous hosting protocols for FDA inspections
MICHR’s strategic approach to recruiting, screening, and enrolling participants in clinical trials
A guide to developing a clinical trial protocol which will stand as the cornerstone of as study, setting out the essential procedures and compliance standards
Principal Investigator (PI) Oversight / Staff Roles and Responsibilities Standard Practice Guideline
A guide to ensure clinical research is conducted safely and accurately by documenting clear roles and responsibilities for each member of the team
A guide to the consent process ensuring compliance with IRBMED, FDA, ICH GCP, and specific sponsor requirements
Strategies to embed compliance in your team operations, optimize communication with participants and address study deviations to safeguard research integrity
Guide to ensure accuracy and safety in your clinical trials with vigilant equipment management, all documented for ready verification and adherence to protocol standards