Uniform MPJE (UMPJE) Content Outline

Learn about the 4 domains covered on the Uniform MPJE (UMPJE), including their weights and subtopics, to align your study plan with the UMPJE blueprint.
Pharmacy student reading the UMPJE content outline

The Uniform Multistate Pharmacy Jurisprudence Examination (UMPJE) is administered by the National Association of Boards of Pharmacy (NABP) to assess applicants' understanding of uniform pharmacy laws that are common across most states. Its specific content areas reflect the tasks, knowledge, skills, and abilities required to apply these laws and regulations. The content outline, or blueprint, below will help identify tested pharmacy topics and their approximate weight, so you can confidently prepare for the exam.

UMPJE Domains and Exam Weights

The UMPJE consists of 4 primary content domains, broken down into 2nd and 3rd-level domains where applicable. Each domain represents a major area of pharmacy law and practice.

UMPJE content domain weights

Every question you see on the exam will be classified under at least 1 of these topic areas. The UMPJE’s 4 domains and their respective exam weights are:

Content Domain Exam Weight (approx. number of questions)
1. Pharmacy and Pharmacist Practice 30% (30 questions)
2. Medication Use Process (Prescribing, Transcribing and Documenting, Dispensing, Administering, and Monitoring) 30% (30 questions)
3. Regulatory Authority and Legal Obligations 20% (20 questions)
4. Pharmacy Operations 20% (20 questions)

Detailed Breakdown of UMPJE Content Areas

The subdomains associated with each primary content area are as follows:

Domain 1: Pharmacy and Pharmacist Practice

  1. Practice of pharmacy definition (e.g., scope of authority, scope of practice, collaborative practice agreements, and other delegative authorities, limitations, or restrictions on practice)
  2. Non-pharmacist personnel (e.g., supervision, scope, licensure, and counseling)
  3. Adulterated or misbranded medications (e.g., medication recalls, expiration dates, counterfeit medications, emergency use authorizations, importation, and the Drug Supply Chain Security Act (DSCSA))
  4. Federal regulatory standards (e.g., National Institute for Occupational Safety and Health (NIOSH), Occupational Safety and Health Administration (OSHA), essential copies of commercial products, patient-specific prescription requirements, and anticipatory compounding)
  5. United States Pharmacopeia (USP) standards on compounding and hazardous materials (e.g., beyond-use dating, competency training, environmental testing, and record keeping)
  6. Security of patient health information

Domain 2: Medication Use Process

  1. Requirements for issuing prescriptions and medication orders, including controlled substances
    1. Validity of a prescription (e.g., authority, content, and corresponding responsibility)
    2. Changes to a prescription
    3. Emergency prescriptions and emergency refills
  2. Dispensing medications, including controlled substances
    1. Pharmacy and manufacturer labeling, including over-the-counter medications and patient education
    2. Drug utilization review
    3. Fills, refills, and partial fills
    4. Packaging and repackaging
    5. Counseling
    6. Transfers
    7. Prescription drug monitoring program (PDMP) requirements
    8. Recalls, returns, and reuse
    9. Drug product selection (e.g., substitutions and interchangeability)
  3. Administration of medications, including adverse event reporting

Domain 3: Regulatory Authority and Legal Obligations

  1. Role of regulatory authorities, including authority, inspections, and discipline
    1. Federal (e.g., Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), and U.S. Department of Health and Human Services (HHS))
    2. State (e.g., board of pharmacy and department of health)
  2. Controlled substances
    1. Inventory
    2. Record keeping
    3. Order forms and ordering
    4. DEA registration and power of attorney
    5. Theft and loss
    6. Disposal
  3. Liability and malpractice

Domain 4: Pharmacy Operations

  1. Licensures, registrations, and certifications
  2. Pharmacy technology, including record keeping and automation (e.g., ePrescribing, faxing, and shared services)
  3. Access, storage, handling, and security
Map of the United States with thousands of students who passed the MPJE with UWorld RxPrep.
Map of the United States with thousands of students who passed the MPJE with UWorld RxPrep.

How UMPJE Content Differs from the MPJE®

Although the UMPJE and the traditional MPJE® share a common focus on pharmacy law competency, the two examinations differ in several meaningful ways. The MPJE is state-specific, whereas the UMPJE focuses on common concepts and general principles of state law. This makes the UMPJE an important resource for states seeking to give pharmacists the flexibility to seek licensure across multiple participating jurisdictions.

MPJE Uniform MPJE
 Federal laws and regulations  Federal laws and regulations
 State-specific laws and regulations  Common state-level principles
 Non-transferable across jurisdictions  Transferable across participating jurisdictions
Check your jurisdiction to see which exam you need to prepare for.

UMPJE Frequently Asked Questions (FAQs)

There are 4 content domains tested on the UMPJE:

  1. Pharmacy and Pharmacist Practice (30% of exam)
  2. Medication Use Process (30% of exam)
  3. Regulatory Authority and Legal Obligations (20% of exam)
  4. Pharmacy Operations (20% of exam)

Yes, the UMPJE requires you to know federal laws and regulations, as well as the concepts and general principles of state law that are common across jurisdictions. For example, the UMPJE content outline covers:

  • Federal regulatory standards (e.g., National Institute for Occupational Safety and Health (NIOSH), Occupational Safety and Health Administration (OSHA), essential copies of commercial products, patient-specific prescription requirements, and anticipatory compounding)
  • Role of federal regulatory authorities (e.g., Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), and U.S. Department of Health and Human Services (HHS))

Yes, any jurisdiction administering the UMPJE will use the same Uniform MPJE Content Outline. This blueprint is maintained by the National Association of Boards of Pharmacy.

The UMPJE content outline was created by the National Association of Boards of Pharmacy. Any future content revisions or updated topic weights will be handled by the NABP with adequate notice for candidates.

We recommend creating a UMPJE study guide using UWorld RxPrep. The UWorld RxPrep MPJE materials, which include a course manual, videos, and Qbank all focused on federal law, will cover the necessary information needed to pass the UMPJE.

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