About CRP QBank
CRP QBank is an independent online exam prep resource built to help clinical research professionals prepare with confidence for CCRP® and ACRP® certification exams. Our platform supports effective studying and stronger exam readiness through realistic practice questions, mock exams, flashcards, and detailed explanations.
Designed for both aspiring and experienced clinical research professionals, CRP QBank covers key topics including Good Clinical Practice (GCP), ICH E6 guidelines, informed consent, safety reporting, ethics, monitoring, essential documents, regulatory concepts, and study operations. Our goal is to help candidates build knowledge, sharpen judgment, and succeed in their certification journey.
CRP QBank is not endorsed by, affiliated with, or approved by SOCRA, ACRP, or any other certification or regulatory body. All materials are provided for educational and study support purposes only.
The QBank Includes:
ICH GCP (International Council for Harmonisation Good Clinical Practice)
Federal Regulations:
Title 45, Part 46: Protection of Human Subjects
Title 21, Part 50: Protection of Human Subjects
Title 21, Part 56: Institutional Review Boards
Title 21, Part 54: Financial Disclosures by Clinical Investigators
Title 21, Part 312: Investigational New Drug Application
Title 21, Part 812: Investigational Device Exemptions
Title 21, Part 11: Electronic Records and Electronic Signatures
In addition to these regulations, the QBank addresses key FDA statutes and duties involved in the regulation of clinical trials, as well as guidance issued by the HRP and the FDA.
Our QBank Comprehensively Covers
Research Study Start-Up
Research Study Implementation
Research Study Closure
Research Study Start-Up
✓ Coordinate the development of initial research study protocol
✓ Create or obtain research study documents (e.g., informed consent, essential documents, case report forms, financial disclosure statements)
✓ Obtain research study approval from necessary stakeholders (i.e., IRB, research study sponsor, and relevant regulatory authorities)
✓ Obtain research study product, related materials, equipment, tools and aids
✓ Select research study sites
✓ Train research study staff members
✓ Evaluate research study’s compliance with relevant local, state and provincial laws
Research Study Implementation
✓ Execute research study in accordance with the protocol
✓ Assure regulatory compliance
✓ Manage research study product (e.g., treatment, procedure, medication, medical device, questionnaire)
✓ Identify, document & report research study anomalies
✓ Manage subjects
✓ Maintain the research study
✓ Communicate with research study stakeholders
✓ Perform/participate in a research study audit
Research Study Closure
✓ Perform/participate in a research study closeout visit
✓ Develop and submit research study closure reports
✓ Archive and retrieve research study records
