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Updated: Oct 26, 2026

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NABP UMPJE Exam Overview:

Certification Vendor:National Association of Boards of Pharmacy (NABP)
Exam Name:Uniform Multistate Pharmacy Jurisprudence Examination (Uniform MPJE™)
Exam Number:UMPJE
Related Certifications:North American Pharmacist Licensure Examination (NAPLEX)
Foreign Pharmacy Graduate Examination Committee Certification (FPGEC)
Exam Format:Selected-response questions, Computer-based examination, Pharmacy law and jurisprudence scenarios
Passing Score:Pass/Fail; numerical passing score not publicly specified
Available Languages:English
Certificate Validity Period:No separate certification validity period; used for pharmacist licensure in participating jurisdictions, subject to applicable board requirements
Real Exam Qty:Not independently verified for UMPJE; consult the current NABP Candidate Application Bulletin
Exam Duration:150 minutes
Recommended Training:Official UMPJE Content Outline
NABP Pre-UMPJE Official Practice Examination
NABP MPJE/UMPJE Exam Preparation Resources
Exam Registration:NABP MPJE/UMPJE Application Instructions
NABP Uniform MPJE Official Information
NABP Candidate Application Bulletin
Exam Way:Computer-based examination administered through the authorized testing process. Candidates must apply for eligibility through NABP and confirm that their intended jurisdiction uses the UMPJE rather than the state-specific MPJE.
Pre Condition:Eligibility is determined by NABP and the applicable state or territorial board of pharmacy. Candidates may include recent pharmacy graduates, pharmacists seeking licensure in another jurisdiction, and FPGEC-certified pharmacists. Specific education, credential, and jurisdictional requirements apply.
Official Syllabus URL:https://nabp.pharmacy/wp-content/uploads/Uniform-MPJE-Content-Outline.pdf

NABP UMPJE Exam Syllabus Topics:

SectionWeightObjectives
Regulatory Authority and Legal Obligations20%- Controlled Substances and Legal Liability
  • 1. Controlled substance inventories, records, ordering, DEA registration, theft and loss reporting, and disposal
    • 2. Professional liability, malpractice, and legal obligations in pharmacy practice
      - Regulatory Authorities
      • 1. State boards of pharmacy, departments of health, and applicable regulatory responsibilities
        • 2. Roles, powers, inspections, and disciplinary authority of federal agencies, including FDA, DEA, and HHS
          Medication Use Process30%- Prescribing and Medication Orders
          • 1. Prescription changes, emergency prescriptions, and emergency refills
            • 2. Prescription validity, prescriber authority, required prescription information, and controlled substances
              - Dispensing and Medication Management
              • 1. Patient counseling, prescription transfers, prescription drug monitoring programs, recalls, returns, and reuse
                • 2. Drug product selection, substitution, interchangeability, medication administration, and adverse event reporting
                  • 3. Labeling, drug utilization review, refills, partial fills, packaging, and repackaging
                    Pharmacy Operations20%- Licensure and Technology
                    • 1. Pharmacy technology, electronic prescribing, faxing, shared services, automation, and record keeping
                      • 2. Pharmacy and personnel licenses, registrations, and certifications
                        - Security and Operational Compliance
                        • 1. Access control, medication storage, handling, and security requirements
                          Pharmacy and Pharmacist Practice30%- Medication Standards and Patient Information
                          • 1. Federal regulatory standards, USP compounding requirements, hazardous materials, and patient health information security
                            • 2. Adulterated or misbranded medications, recalls, expiration dates, counterfeit drugs, and drug supply chain security
                              - Practice of Pharmacy and Personnel
                              • 1. Scope of practice, collaborative practice agreements, delegated authority, and practice restrictions
                                • 2. Supervision, qualifications, licensure, and responsibilities of non-pharmacist personnel

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