
The ACRP Medical Device Professional (ACRP-MDP) is a professional specialty credential offered by the Association of Clinical Research Professionals. It evaluates the ability to protect research participants, apply medical device regulations, oversee clinical trial operations, manage study sites, maintain reliable data, and assess scientific and research-design considerations.
The specialty is typically pursued by clinical research coordinators, clinical research associates, principal investigators, and other ACRP-certified professionals working with medical device trials. The exam contains 60 multiple-choice questions, including 10 unscored pretest questions, and is completed in 90 minutes. These FAQs explain the credential’s purpose, format, passing standard, renewal requirements, preparation considerations, ethical expectations, and the role of simulation-based practice.
ACRP-MDP — Frequently Asked Questions (FAQs)
This FAQ section summarizes key aspects of the ACRP-MDP exam, including format, difficulty, and preparation. For official eligibility, policies, and updates, visit the ACRP’s official exam page.
SECTION A: ACRP-MDP Exam Overview & Legitimacy
This section explains what the ACRP-MDP specialty credential represents, who typically pursues it, and which professional competencies it evaluates. It also distinguishes the credential from licensure or independent legal authority.
Q1. What is the ACRP Medical Device Professional certification?