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Clinical Research Acronyms & Flashcards

A quick-reference glossary of clinical research abbreviations plus an interactive flashcard tool for CCRC and CCRP exam preparation.

80+ acronyms | 52 flashcards | Filterable by category | Certification Guide

Acronym Glossary

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Definitions reflect current clinical research practice. Some terms may vary by protocol, sponsor, or jurisdiction.

Studying for your CCRC or CCRP? See our complete Certification Guide for fact-checked requirements, study strategies, and recommended books, including the official ICH E6(R3) guideline and exam prep study guides.

Interactive Flashcards

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Definitions reflect ICH GCP E6(R3) and current U.S. clinical research practice. Always verify against your study protocol and current regulatory guidance.

Professional Reference Books

Reference books used across the clinical research field. For exam content outlines, check ACRP and SOCRA directly.

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CRC Operations & Site Reference

Budget Pick Conducting Clinical Research — Judy Stone, MD Practical site-level guide to recruiting participants, implementing protocols, and navigating regulatory requirements. Accessible for new coordinators. View on Amazon → Premium Pick Clinical Research Coordinator Handbook, 5th Ed. — Norris The standard CRC reference — federal regulations, GCP, informed consent, source documentation, EDC, adverse event reporting, and regulatory inspection preparation. Forms and checklists included. View on Amazon → Free Official Source ICH E6(R3) — GCP Guideline (PDF) The current GCP standard, finalized January 2025. Free PDF from the ICH website. Reading the actual guideline is more valuable than any summary of it. Download Free PDF →

Trial Design & Broader Methods

Budget Pick Fundamentals of Clinical Trials, 5th Ed. — Friedman et al. Standard academic text on trial design — randomization, blinding, endpoints, and statistical considerations. Older editions widely available at lower cost. View on Amazon → Premium Pick Principles and Practice of Clinical Research, 4th Ed. — Gallin et al. Comprehensive academic reference covering bioethics, trial design, regulatory frameworks, and the full scope of clinical investigation. Suited for professionals moving into PI or management roles. View on Amazon →
Free Official Sources Regulatory Texts

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More Study Resources

Certification Guide Belmont Report & Ethics Informed Consent Guide Adverse Event Reporting Source Documentation All Resources & Books