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Key Facts: CMPP Exam

150

Questions

ISMPP

3 hours

Exam Duration

ISMPP

~80%

First-Attempt Pass Rate

ISMPP

$595

Member Exam Fee

ISMPP

5 years

Certification Validity

ISMPP Recertification

50 credits

CE Recertification Total

ISMPP Recertification

The CMPP is a 150-question, 3-hour, multiple-choice exam administered by ISMPP through Pearson VUE testing centers and OnVUE. Eligibility requires either a bachelor's degree plus 2 years (4,000 hours) of relevant experience or a high school diploma plus 5 years (10,000 hours). The exam fee is $595; non-members pay an additional $235 administrative fee that includes membership, candidates from developing countries pay $395, and retakes cost $250. The three blueprint domains receive equal question distribution. Certificants qualifying or recertifying from 2022 onward have a 5-year cycle and must earn 50 continuing education credits or pass the examination again. Current core references include GPP 2022, the ICMJE Recommendations, the 2024 Declaration of Helsinki, the EQUATOR reporting guidelines, GPCAP 2026, trial-transparency requirements, Open Payments, and relevant regional codes and laws.

Sample CMPP Practice Questions

Try these sample questions to review concepts for the CMPP exam. Each question includes a detailed explanation. Start the interactive quiz above for the full 100+ question experience with AI tutoring.

1According to the ICMJE authorship criteria, how many criteria must an individual meet to qualify as an author on a manuscript?
A.All 4 criteria
B.At least 2 of 4 criteria
C.Any 3 of 4 criteria
D.Only substantial contribution to study design
Explanation: The ICMJE Recommendations require that an author meet ALL four criteria: (1) substantial contributions to the conception or design of the work, or the acquisition, analysis, or interpretation of data; (2) drafting the work or revising it critically for important intellectual content; (3) final approval of the version to be published; and (4) agreement to be accountable for all aspects of the work. Meeting only some of the criteria is not sufficient for authorship.
2Under Good Publication Practice (GPP 2022), what is the appropriate way to recognize a professional medical writer who assisted with drafting a manuscript but did not meet ICMJE authorship criteria?
A.Named acknowledgment including their role, affiliation, and funding source
B.No recognition is necessary because they were paid
C.Listed as a non-author contributor only if the journal specifically asks
D.Include as a corresponding author but note their writing role
Explanation: GPP 2022 (the fourth iteration, often called GPP 2022 or the update to GPP3) and ICMJE both require that professional medical writers who do not meet authorship criteria be clearly acknowledged by name, with their role described (e.g., 'drafted the first version of the manuscript'), their affiliation stated, and the source of funding for their writing assistance disclosed. Hiding medical writer involvement is considered ghostwriting and is a form of research misconduct.
3Which reporting guideline should be used for a randomized controlled trial (RCT)?
A.CONSORT
B.PRISMA
C.STROBE
D.ARRIVE
Explanation: CONSORT (Consolidated Standards of Reporting Trials) is the reporting guideline for randomized controlled trials. The current version, CONSORT 2010, includes a 25-item checklist and a flow diagram. PRISMA is for systematic reviews and meta-analyses, STROBE is for observational studies, and ARRIVE is for preclinical animal research. The EQUATOR Network hosts all these guidelines.
4Per ICMJE, when must a clinical trial be registered for the results to be eligible for publication?
A.Prospectively, before enrollment of the first participant
B.Within 60 days of the first patient visit
C.Before database lock
D.Before the manuscript is submitted
Explanation: ICMJE requires prospective registration of clinical trials in a publicly accessible registry (e.g., ClinicalTrials.gov, EudraCT, ISRCTN) before enrollment of the first participant as a condition of consideration for publication. Retrospective registration is not acceptable to most ICMJE-compliant journals. This policy was adopted in 2005 to combat selective reporting and publication bias.
5A medical writer drafts a manuscript for an industry-sponsored trial without being named in the acknowledgments, and no writing assistance is disclosed. This is an example of:
A.Ghostwriting
B.Guest authorship
C.Honorary authorship
D.Duplicate publication
Explanation: Ghostwriting occurs when an individual (such as a professional medical writer) makes substantial contributions to a publication without being named as an author or acknowledged. It is considered a breach of publication ethics by ICMJE, WAME, GPP 2022, and the AMWA Code of Ethics. Guest authorship is the opposite problem: naming someone as an author who did not meet ICMJE criteria. Both practices compromise the integrity of the scientific literature.
6Which organization maintains the EQUATOR Network library of reporting guidelines?
A.A nonprofit network based at the University of Oxford
B.The International Committee of Medical Journal Editors (ICMJE)
C.The World Health Organization
D.The U.S. Food and Drug Administration
Explanation: The EQUATOR (Enhancing the QUAlity and Transparency Of health Research) Network is a nonprofit international initiative hosted at the UK EQUATOR Centre (based at the University of Oxford). It maintains a comprehensive online library of reporting guidelines including CONSORT, PRISMA, STROBE, CARE, SPIRIT, ARRIVE, STARD, and many others. It is not operated by ICMJE, WHO, or FDA.
7Under GPP 2022, who has ultimate responsibility for ensuring the publication is accurate, transparent, and compliant with guidelines?
A.All authors collectively, with the sponsor/company ensuring processes support compliance
B.The corresponding author alone
C.The medical writer engaged for the project
D.The journal editor and peer reviewers
Explanation: GPP 2022 specifies that authors have collective responsibility for the accuracy, completeness, and transparency of the publication, while sponsors (e.g., pharmaceutical companies) are responsible for ensuring that processes, resources, and training support compliance with publication guidelines. Medical writers assist but cannot replace author responsibility, and journal editors/reviewers assess quality but are not primarily responsible for content accuracy.
8A publication plan is typically developed at which stage of a compound's lifecycle?
A.Before Phase 3 pivotal trials, ideally during Phase 2 or earlier
B.Only after regulatory approval
C.At the time of manuscript submission
D.After the first commercial launch
Explanation: Effective publication planning begins early in the compound's lifecycle, ideally during or before Phase 2 development and well before the pivotal Phase 3 trials are complete. Early planning allows for coordination of scientific communication, congress abstracts, primary manuscripts, secondary analyses, and post-marketing publications in a transparent, strategic manner. Waiting until regulatory approval or manuscript submission is too late.
9According to ClinicalTrials.gov reporting requirements under the Final Rule (42 CFR Part 11), when must summary results typically be posted after the primary completion date?
A.Within 12 months
B.Within 6 months
C.Within 24 months
D.At the time of publication only
Explanation: The FDAAA 801 Final Rule (42 CFR Part 11) requires that summary results information for applicable clinical trials be submitted to ClinicalTrials.gov no later than 12 months after the primary completion date, regardless of whether the results have been published. Extensions may be granted under specific circumstances. Failure to comply can result in civil monetary penalties and withholding of NIH grant funds.
10Which reporting guideline is designed for systematic reviews and meta-analyses?
A.PRISMA
B.CONSORT
C.STROBE
D.SPIRIT
Explanation: PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) is the standard reporting guideline for systematic reviews and meta-analyses. PRISMA 2020 replaced the original 2009 statement and includes a 27-item checklist and flow diagram. CONSORT is for RCTs, STROBE is for observational studies, and SPIRIT is for clinical trial protocols.

About the CMPP Exam

The ISMPP CMPP (Certified Medical Publication Professional) credential is the only certification designed specifically for professionals working in medical publications — medical writers, publication planners, editors, and agency or pharma publication staff. The exam tests knowledge of publication planning, development, ethics, disclosure/transparency, and post-publication metrics, grounded in GPP 2022, ICMJE Recommendations, CONSORT/PRISMA/STROBE/SPIRIT/ARRIVE reporting guidelines, and global regulatory frameworks.

Exam sponsor: ISMPP. The requirements and fees below concern the certification or admission exam, separate from our free practice resources.

Questions

150 questions

Time Limit

3 hours

Passing Score

650 on a 0–900 scaled score

Exam / Certification Fees

$595 (members) / $595 + $235 admin fee (non-members)

Exam sponsor website

Reported exam pass rate: ~80%. ISMPP reports approximately 80% of candidates pass on first attempt This describes exam candidates, not OpenExamPrep users or results from using our resources. 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.

~33.3% (equal domain distribution)

Developing a Publication Plan

Eight duties: research the disease and therapeutic landscape; identify publishable data and audience needs; define plan scope; manage a publication steering committee; apply the scientific communication platform; develop the tactical plan; and monitor evolving trends

~33.3% (equal domain distribution)

Implementing a Publication Plan

Five duties: identify and engage authors and contributors; apply appropriate writing, review, and approval processes; manage administrative aspects; track plan-level and publication-level metrics; and monitor evolving trends

~33.3% (equal domain distribution)

Fostering Ethical and Compliant Behavior

Five duties: maintain current knowledge of standards, guidelines, and position statements; apply ethical-conduct standards; ensure appropriate disclosures; ensure appropriate contributor acknowledgment; and monitor evolving trends

Preparing for the CMPP Exam

What You Need to Know

  • Passing score: 650 on a 0–900 scaled score
  • Exam length: 150 questions
  • Time limit: 3 hours
  • Exam / certification fees: $595 (members) / $595 + $235 admin fee (non-members) Official sources

Using Our Practice Resources

  • Work through all 100 available questions
  • Review every answer and explanation
  • Track weak areas and revisit them
  • Use our AI tutor for tough concepts

CMPP: Suggested Study Strategy

1Read GPP 2022 carefully — it is a current CMPP critical reference for company-sponsored biomedical publications
2Memorize the 4 ICMJE authorship criteria (contribution, drafting/revising, final approval, accountability) — you must meet ALL four to qualify as an author
3Learn the EQUATOR Network reporting guidelines by study type: CONSORT (RCTs), PRISMA (systematic reviews), STROBE (observational), SPIRIT (protocols), ARRIVE (animal), STARD (diagnostic), CARE (case reports)
4Study trial registration and results-disclosure frameworks by scope and jurisdiction, including FDAAA 801, EU CTR/CTIS, and ICMJE prospective registration policy; verify the deadline that applies to the specific trial
5Understand how scientific and promotional communications are distinguished under the applicable FDA, EU, national, and industry-code frameworks
6Complete at least 2-3 full-length timed practice exams before your test window to build pacing and identify weak areas
7Use the official 2026 CMPP Study Guide and current Critical Reference List to organize study by all 18 blueprint duties

Frequently Asked Questions

What is the ISMPP CMPP exam format?

The CMPP exam consists of 150 psychometrically validated multiple-choice questions delivered by Pearson VUE, either at a Pearson VUE testing center or online via OnVUE proctored delivery. You have 3 hours to complete the exam. It is a pass/fail credential based on a criterion-referenced scaled score. Approximately 80% of candidates pass on first attempt.

Who is eligible to take the CMPP exam?

ISMPP requires either a bachelor's degree plus 2 years (4,000 hours) of relevant medical publication experience, OR a high school diploma plus 5 years (10,000 hours) of relevant experience. Candidates must also hold ISMPP membership (or pay a $235 non-member administrative fee that includes one year of membership). Relevant experience includes medical writing, publication planning, editorial work, and publication management at pharmaceutical companies, agencies, or CROs.

How much does the CMPP exam cost in 2026?

The CMPP exam fee is $595 for ISMPP members. Non-members pay $595 plus a $235 administrative fee (which includes one year of ISMPP membership), for a total of $830. Candidates from developing countries pay a reduced fee of $395. Retakes within the next testing window cost $250. Fees are set by ISMPP and are subject to change — always verify on the official ISMPP exam details page.

What content does the CMPP exam cover?

The current blueprint has three equally weighted competency domains: (1) developing a publication plan, with eight duties; (2) implementing a publication plan, with five duties; and (3) fostering ethical and compliant behavior, with five duties. The official 2026 study guide lists all 18 duties. Current critical references include GPP 2022, the ICMJE Recommendations, the Declaration of Helsinki, EQUATOR reporting guidelines, GPCAP 2026, and applicable transparency and regulatory frameworks.

How long should I study for the CMPP exam?

ISMPP does not publish a required study-hour total. Build an individualized plan from the official 2026 Study Guide and current Critical Reference List, concentrating on duties outside your daily role. Use primary sources rather than memorizing a fixed hour estimate: GPP 2022, the current ICMJE Recommendations, CONSORT 2025, SPIRIT 2025, PRISMA 2020, GPCAP 2026, and the applicable ethics, transparency, and regulatory materials.

What are the CMPP recertification requirements?

For people certifying or recertifying from 2022 onward, the CMPP cycle is 5 years. Recertification requires 50 approved continuing education credits or successful re-examination. The credit pathway requires at least 5 credits in each of the three blueprint domains, at least 5 credits in each year of the cycle, no more than 8 self-paced credits in a year, and active publication practice during at least 3 years of the cycle. Use the current ISMPP Recertification Handbook for activity, documentation, deadline, fee, and audit rules.

Is CMPP recognized worldwide?

Yes. The CMPP is an international credential specific to medical publication professionals. ISMPP's official 2026 examination study guide describes certificants in 30 countries across six continents. Candidates should use the credentialing body's current figures rather than extrapolating an unsupported country or certificant count.

What is GPP 2022 and why is it important for the CMPP exam?

GPP 2022 is the current Good Publication Practice guidance for company-sponsored biomedical research. It addresses publication planning and development, authorship and contributorship, professional medical writing support, sponsor involvement, agreements, and transparency. ISMPP includes it on the current CMPP Critical Reference List; the exam body does not publish an item count for any individual reference.