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Exam Review

Key Facts: RI MPJE Exam

120

Exam Questions

100 scored + 20 pretest

75

Passing Score

Scaled score

2.5 hrs

Time Limit

NABP

15

CE Hours

Per renewal period

30-dose/7-day supply (whichever is less)

Initial Opioid Limit

Rhode Island acute pain

1,500 hours

Intern Hours Required

RI Board

The RI MPJE covers federal pharmacy law (DEA, FDA, CSA, HIPAA) and Rhode Island-specific regulations including RI PMP, 15 CE hours per calendar year, pharmacist immunization authority for patients 9+, naloxone standing orders, and pending legislation for pharmacist prescribing of tobacco cessation and contraceptive medications. The RI Board of Pharmacy operates under the Department of Health.

Sample RI MPJE Practice Questions

Try these sample questions to review concepts for the RI MPJE exam. Each question includes a detailed explanation. Start the interactive quiz above for the full 299+ question experience with AI tutoring.

1Under the Controlled Substances Act (CSA), which DEA schedule includes drugs with the highest potential for abuse and no currently accepted medical use?
A.Schedule I
B.Schedule II
C.Schedule III
D.Schedule IV
Explanation: Schedule I substances have a high potential for abuse, no currently accepted medical use in treatment in the United States, and a lack of accepted safety for use under medical supervision. Examples include heroin, LSD, and MDMA. Pharmacists cannot dispense Schedule I substances under normal practice.
2A DEA Form 222 is required for the transfer of which schedule of controlled substances between registrants?
A.Schedule II only
B.Schedules II and III
C.Schedules III through V
D.All controlled substances
Explanation: DEA Form 222 (or its electronic equivalent under CSOS) is required for the distribution and transfer of Schedule II controlled substances between DEA registrants. Schedules III-V can be transferred using invoices with specific record-keeping requirements.
3Under federal law, what is the maximum number of refills allowed for a Schedule III controlled substance prescription?
A.No refills allowed
B.Up to 3 refills within 6 months
C.Up to 5 refills within 6 months
D.Up to 5 refills within 1 year
Explanation: Federal law allows up to 5 refills for Schedule III-V controlled substance prescriptions within 6 months from the date the prescription was issued. Schedule II prescriptions cannot be refilled. After 6 months or 5 refills, a new prescription is required.
4The Durham-Humphrey Amendment of 1951 established which key distinction in drug classification?
A.Generic vs. brand-name drugs
B.Prescription (legend) vs. over-the-counter drugs
C.Controlled vs. non-controlled substances
D.Biological vs. chemical drugs
Explanation: The Durham-Humphrey Amendment to the Federal Food, Drug, and Cosmetic Act (FDCA) established the distinction between prescription (legend) drugs and over-the-counter (OTC) drugs. It required that certain drugs be dispensed only with a valid prescription and bear the legend 'Caution: Federal law prohibits dispensing without prescription.'
5Under the Poison Prevention Packaging Act (PPPA), which of the following medications is EXEMPT from child-resistant packaging requirements?
A.Acetaminophen tablets
B.Sublingual nitroglycerin tablets
C.Amoxicillin suspension
D.Hydrocodone/acetaminophen tablets
Explanation: Sublingual nitroglycerin tablets are exempt from child-resistant packaging under the PPPA because they require immediate access during cardiac emergencies. Other exemptions include oral contraceptives in manufacturer dispensing packages, certain hormone replacement therapy, and isosorbide dinitrate sublingual tablets.
6What is the primary purpose of the FDA's Risk Evaluation and Mitigation Strategies (REMS) program?
A.To reduce drug manufacturing costs
B.To ensure the benefits of a drug outweigh its risks
C.To speed up the drug approval process
D.To establish drug pricing guidelines
Explanation: REMS are drug safety programs required by the FDA for certain medications with serious safety concerns. They help ensure the benefits of a medication outweigh its risks. REMS may include medication guides, communication plans, and Elements to Assure Safe Use (ETASU) such as prescriber certification and patient registries.
7Under the Combat Methamphetamine Epidemic Act (CMEA), what is the maximum amount of pseudoephedrine a customer can purchase in a 30-day period?
A.3.6 grams
B.7.5 grams
C.9 grams
D.15 grams
Explanation: The CMEA limits pseudoephedrine purchases to 3.6 grams per day and 9 grams per 30-day period for retail transactions. Mail-order purchases are limited to 7.5 grams per 30-day period. Retailers must keep a logbook of all pseudoephedrine sales and products must be kept behind the counter.
8A pharmacist receives a prescription for a Schedule II controlled substance dated 45 days ago. Under federal law, this prescription:
A.Must be filled within 30 days
B.May be filled as there is no federal time limit
C.Cannot be filled because it has expired
D.May only be partially filled
Explanation: Federal law does not impose a specific time limit on filling Schedule II prescriptions. However, many states, including New Jersey, may impose their own time limits. The pharmacist must use professional judgment to determine whether the prescription is still valid based on the patient's needs and state law requirements.
9Under the Health Insurance Portability and Accountability Act (HIPAA), which of the following is NOT considered protected health information (PHI)?
A.A patient's prescription history
B.A patient's date of birth
C.De-identified aggregate prescription data
D.A patient's home address
Explanation: De-identified data is not considered PHI under HIPAA. PHI includes individually identifiable health information such as names, dates, addresses, Social Security numbers, and medical records. Data that has been properly de-identified according to HIPAA standards (Safe Harbor or Expert Determination method) is not subject to HIPAA restrictions.
10Under the Drug Supply Chain Security Act (DSCSA), what must be included with each transaction of a prescription drug between trading partners?
A.Only the drug name and NDC number
B.Transaction information, transaction history, and transaction statement
C.DEA Form 222 and invoice
D.Certificate of analysis and lot number only
Explanation: The DSCSA requires three types of documentation for each prescription drug transaction: transaction information (drug details, date, entities involved), transaction history (previous ownership chain), and transaction statement (attestation that the trading partner meets DSCSA requirements). This supports drug supply chain integrity and helps prevent counterfeit drugs.

About the RI MPJE Exam

The RI MPJE tests knowledge of federal pharmacy law and Rhode Island-specific pharmacy regulations. Required alongside the NAPLEX for pharmacist licensure in Rhode Island.

Exam sponsor: NABP / Rhode Island Board of Pharmacy (under RI Department of Health). The requirements and fees below concern the certification or admission exam, separate from our free practice resources.

Questions

120 questions

Time Limit

2.5 hours

Passing Score

75 (scaled score)

Exam / Certification Fees

$250

Exam sponsor website

Reported exam pass rate: Not publicly reported. Exam sponsor website

Fees, eligibility, and exam policies can change. Confirm them with the exam sponsor before applying or paying.

Our practice resources: topics covered

We aim to reflect publicly available exam outlines and topic information in our study resources. Coverage, format, and difficulty may differ from the actual exam, and we cannot guarantee that every detail is accurate or current. Confirm exam requirements, fees, and policies with the official exam sponsor.

22%

Licensure & Personnel

Pharmacist qualifications, intern/technician requirements, license renewal, disciplinary actions

33%

Pharmacist Practice

Prescription requirements, counseling, collaborative practice, immunizations

24%

Dispensing Requirements

Generic substitution, prescription transfers, DUR, labeling, RI PMP compliance

21%

Pharmacy Operations

Controlled substance records, compounding, pharmacy permits, automated dispensing

Preparing for the RI MPJE Exam

What You Need to Know

  • Passing score: 75 (scaled score)
  • Exam length: 120 questions
  • Time limit: 2.5 hours
  • Exam / certification fees: $250 Official sources

Using Our Practice Resources

  • Work through all 299 available questions
  • Review every answer and explanation
  • Track weak areas and revisit them
  • Use our AI tutor for tough concepts

RI MPJE: Suggested Study Strategy

1Master R.I. Gen. Laws Chapter 5-19.1 and 216-RICR-40-15-1 and Rhode Island pharmacy regulations
2Know RI PMP (Rhode Island Prescription Monitoring Program) requirements for controlled substance dispensing
3Study Rhode Island CE requirements: 15 contact hours per calendar year with 1 hour of pharmacy law per year
4Understand Rhode Island pharmacist-to-technician ratios: 1:2
5Review Rhode Island opioid prescribing limits: 30-dose/7-day supply (whichever is less)

Frequently Asked Questions

What is the RI MPJE exam format?

The RI MPJE is a computer-adaptive test with 120 questions (100 scored, 20 pretest). You have 2.5 hours. A scaled score of 75 or higher is required to pass.

What Rhode Island-specific topics are tested?

Key topics include R.I. Gen. Laws Chapter 5-19.1 and 216-RICR-40-15-1, the RI PMP (Rhode Island Prescription Monitoring Program), 15 contact hours per calendar year with 1 hour of pharmacy law per year, 30-dose/7-day supply (whichever is less) initial opioid limit, pharmacist immunization authority for patients 9+ with pharmacist training, and naloxone access provisions.

How do I register for the RI MPJE?

Register through NABP at nabp.pharmacy. Create an e-Profile, apply for the RI MPJE, pay fees ($100 application + $150 exam), and schedule at a Pearson VUE center.

What happens if I fail the RI MPJE?

You must wait at least 30 days before retaking. Reapplication and fees are required for each attempt.

How long should I study for the RI MPJE?

Most candidates study 2-4 weeks. Focus on R.I. Gen. Laws Chapter 5-19.1 and 216-RICR-40-15-1, federal law, and scenario-based practice questions.

Does Rhode Island require EPCS?

Rhode Island permits but does not mandate electronic prescribing for controlled substances. E-prescriptions must comply with DEA EPCS requirements under 21 CFR Part 1311.