Exam Code: UMPJE-PNP-2
Exam Name: Uniform MPJE™
Certification Provider: NABP
Corresponding Certification: NABP Certification

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Updated: Oct 25, 2026

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NABP UMPJE-PNP-2 Exam Overview:

Certification Vendor:	National Association of Boards of Pharmacy (NABP)
Exam Name:	Uniform Multistate Pharmacy Jurisprudence Examination (UMPJE)
Exam Number:	UMPJE-PNP-2
Exam Format:	Computer-adaptive testing, Computer-based examination, Selected-response questions
Certificate Validity Period:	Not applicable; the UMPJE is a pharmacist licensure examination, not a time-limited certification
Passing Score:	Pass/Fail; numerical passing threshold not confirmed in the official public outline
Available Languages:	English
Related Certifications:	Foreign Pharmacy Graduate Examination Committee Certification (FPGEC)
Exam Duration:	150 minutes
Real Exam Qty:	120 questions (100 scored and 20 unscored pretest questions; verify against the current UMPJE candidate bulletin)
Exam Way:	Computer-based examination administered through the authorized examination delivery process. Consult the current NABP Candidate Application Bulletin and the relevant state board of pharmacy for registration, scheduling, and delivery requirements.
Pre Condition:	Eligibility is determined by the applicable participating state board of pharmacy and NABP requirements. Candidates may include recent pharmacy graduates, licensed pharmacists seeking licensure in another jurisdiction, and pharmacists certified by the Foreign Pharmacy Graduate Examination Committee (FPGEC). Requirements vary by jurisdiction.
Official Syllabus URL:	https://nabp.pharmacy/wp-content/uploads/Uniform-MPJE-Content-Outline.pdf

NABP UMPJE-PNP-2 Exam Syllabus Topics:

Section	Weight	Objectives
Topic 1: Medication Use Process (Prescribing, Transcribing and Documenting, Dispensing, Administering, and Monitoring)	30%	- Administration of medications 1. Adverse event reporting - Dispensing medications, including controlled substances 1. Recalls, returns, and reuse 2. Pharmacy and manufacturer labeling, including over-the-counter medications and patient education 3. Fills, refills, and partial fills 4. Transfers 5. Prescription drug monitoring program (PDMP) requirements 6. Counseling 7. Packaging and repackaging 8. Drug product selection, including substitutions and interchangeability 9. Drug utilization review - Requirements for issuing prescriptions and medication orders, including controlled substances 1. Emergency prescriptions and emergency refills 2. Changes to a prescription 3. Validity of a prescription, including authority, content, and corresponding responsibility
Topic 2: Pharmacy Operations	20%	- Pharmacy technology, including record keeping and automation 1. Shared services 2. Faxing 3. Electronic prescribing - Licensures, registrations, and certifications - Access, storage, handling, and security
Topic 3: Pharmacy and Pharmacist Practice	30%	- Non-pharmacist personnel 1. Supervision 2. Scope of practice and licensure 3. Counseling - United States Pharmacopeia (USP) standards on compounding and hazardous materials 1. Environmental testing 2. Record keeping 3. Beyond-use dating 4. Competency training - Adulterated or misbranded medications 1. Counterfeit medications 2. Emergency use authorizations and importation 3. Medication recalls and expiration dates 4. Drug Supply Chain Security Act (DSCSA) - Practice of pharmacy definition 1. Scope of authority and scope of practice 2. Limitations or restrictions on practice 3. Collaborative practice agreements and other delegative authorities - Security of patient health information - Federal regulatory standards 1. Patient-specific prescription requirements 2. Anticipatory compounding 3. National Institute for Occupational Safety and Health (NIOSH) 4. Essential copies of commercial products 5. Occupational Safety and Health Administration (OSHA)
Topic 4: Regulatory Authority and Legal Obligations	20%	- Role of regulatory authorities, including authority, inspections, and discipline 1. State regulatory authorities Boards of pharmacy Departments of health 2. Federal regulatory authorities Food and Drug Administration (FDA) Drug Enforcement Administration (DEA) U.S. Department of Health and Human Services (HHS) - Controlled substances 1. DEA registration and power of attorney 2. Record keeping 3. Theft and loss 4. Disposal 5. Inventory 6. Order forms and ordering - Liability and malpractice

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