Resources
Explore free tools and templates created by Axiom Clinical Consulting to support better trial operations, protocol design, and site training.
Stay compliant with confidence—no overthinking required.
GCP Quick-Reference Guide
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This one-page guide is designed for coordinators, investigators, and research staff who need a fast, practical reminder of core Good Clinical Practice (GCP) principles. It’s not a full training—it’s the high-level, everyday essentials your team needs to protect participants, stay audit-ready, and keep trials running smoothly.
Ensure your protocol is submission-ready—clear, compliant, and built to last.
Protocol Quality Checklist
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This 10-point checklist helps research teams perform a focused, final review of their clinical trial protocols before submission. It highlights the most common problem areas in study design, documentation, and compliance—offering clear prompts to reduce delays, protocol amendments, and reviewer pushback.
Want the full explanation? Read the article
Site Training Essentials
Plan clear, engaging protocol training sessions that actually stick.
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This high-level planning checklist is built for sponsors, CROs, and site leads developing and delivering protocol training. Whether it’s your first investigator meeting or a mid-study refresher, this quick guide helps ensure your sessions are focused, practical, and retention-friendly.
Recommended External Resources
The official Good Clinical Practice guidelines published by the International Council for Harmonisation.
U.S. FDA portal for clinical trial regulations, forms, and guidance for industry.
European Medicines Agency site for EU clinical trial regulations and submission guidance.
Official structure and required elements for protocol registration on ClinicalTrials.gov.
Global standard for trial registration and transparency.
Industry-supported templates for SOPs, training, and risk-based monitoring.