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ClinIQ Academy Catalog

Our resources are built to help you navigate clinical research with clarity and confidence. From binder-ready printables to microlearning sessions and full courses, every tool is anchored in regulations, best practices, and standards — and created for real-world use in daily research.

Some Topics in Development

  • ​Good Documentation Practices

  • FDA Form 1572 & Investigator Responsibilities

  • IP/Device Accountability

  • Informed Consent Best Practices

  • Human Research Protection Training

  • ​Essential Documents Checklist

  • Safety Reporting

  • Participant Records Timeline

  • ​ISO 14155:2020

  • ICH E6 (R3) for sites

Top 5 FDA Findings

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