100% tevredenheidsgarantie Direct beschikbaar na betaling Zowel online als in PDF Je zit nergens aan vast
logo-home
Eerder door jou gezocht
Eerder door jou gezocht
logo
ACRP CP EXAM 2024 €12,17   In winkelwagen
Snel navigeren naar
Voorbeeld
  2.  
  3. ACRP CP
  4.  
  5. ACRP CP

Tentamen (uitwerkingen)

ACRP CP EXAM 2024

1 beoordeling
 18 keer bekeken  0 keer verkocht
  • Vak
  • ACRP CP
  • Instelling
  • ACRP CP

ACRP CP EXAM 2024 | ACCURATE 2 CURRENTLY TESTING EXAMS WITH A STUDY GUIDE AND KNOWLEDGE CHECK FLASHCARDS WITH SUMMARIZED INSTRUCTOR NOTES AT THE END FOR A GUARANTED PASS

Voorbeeld 4 van de 128  pagina's

Document informatie

  • 10 juli 2024
  • 128
  • 2023/2024
  • Tentamen (uitwerkingen)
  • Vragen en antwoorden

Onderwerpen

  • acrp
  • cp exam
  • accurate 2
  • currently testing
  • a study guide
  • knowledge check flashcards
  • summarized instructor notes

Geschreven voor

  • ACRP CP
Alle documenten voor dit vak (298)

1  beoordeling

review-writer-avatar

Door: RegisteredNurse • 3 maanden geleden

Very Informative, detailed and timely, I passed, thank you very much

Verkoper

avatar-seller
DrBellaPhD

Ontvangen beoordelingen

Voorbeeld van de inhoud

ACRP CP EXAM 2024 | ACCURATE 2 CURRENTLY TESTING
EXAMS WITH A STUDY GUIDE AND KNOWLEDGE CHECK
FLASHCARDS WITH SUMMARIZED INSTRUCTOR NOTES
AT THE END FOR A GUARANTED PASS
Who is ultimately responsible for Source Data Verification (SDV)?
A. The coordinator
b. The subject
c. The monitor
d. The investigator
C
Every research study involving human subjects must be registered in a publicly accessible
database
before recruitment of the first subject.
A. True b. False
A
The Declaration of Helsinki was developed by:
a. The Nuremberg tribunal
b. The World Medical Association
c. The government of Finland
d. The American Medical Association
B
This phase determines therapeutic benefit and is usually done in a larger, specific population.
A. Phase 1
b. Phase 2
c. Phase 3
d. Phase 4
C
This phase begins after drug approval and explores therapeutic use:
a. Phase 1
b. Phase 2
c. Phase 3
d. Phase 4
D
This is the most typical study. Investigates human pharmacology. It is the initial administration
or an
investigational new drug into humans. It is most commonly done in healthy subjects.

,A. Phase 1
b. Phase 2
c. Phase 3
d. Phase 4
A
Providing a unified standard for Europe US, and Japan to facilitate the acceptance of clinical
trials is
the...
A. Mission statement of the ICH
b. Mission statement of the Declaration
of Helsinki
c. Mission statement of the GCP Guidelines
d. Mission statement of Canada Health
A
An investigator can be defined as... (Select all that apply)
a. A person responsible for the conduct of the clinical trial with the sponsor
b. A person responsible for writing the trial protocol
c. The responsible leader of the clinical research team at the site and may be called the
principal investigator
d. A person responsible for the conduct of the clinical trial at that site
C, d
A sub-investigator can be defined as...
A. The clinical research coordinator (CRC) or clinical trial nurse
b. Any individual member of the clinical trial team designated and supervised by the investigator
at a trial site to perform critical trial-related procedures and/or to make important trial-related
decisions
c. Any individual member of the clinical trial team supervised by the investigator at a trial site to
perform trial-related procedures
d. Any individual member of the clinical trial team that performs trial related duties
B
A sponsor can be defined as...
A. An individual who both initiates and conducts, alone or with others, a clinical trial
b. An individual who participates in a clinical trial
c. An individual or juridical or other body authorized under applicable law to consent to the
subject's participation in the clinical trial
d. An individual, company, institution, or organization which takes responsibility for the
initiation,
management, and/or financing a clinical trial

,D
What is the purpose of ICH-GCP?
A. To standardize the design, conduct, recording, and reporting of clinical trials
b. To instruct clinicians as to how to conduct preclinical toxicology tests
c. To ensure that subjects are treated with the best available therapy
d. To increase the number of abbreviations used in clinical practice
A
What is the purpose of the IRB/IEC?
A. To help ensure that trials are
conducted according to the protocol
b. To monitor clinical trials
c. To design trial protocols
d. To protect subject safety
D
According to ICH, the abbreviation 'LAR' stands for 'Legally authorized Representative'.
A. True b. False
B
What is the minimum number of members on an IRB/IEC?
A. 3
b. 5
c. 7
d. 8
B
Who is responsible for providing the trial protocol?
A. The sponsor
b. The investigator
c. The IRB/IEC
d. The Institution
A
What does 'DSMB' stand for?
A. Data Record Monitoring Board
b. Drug Statistics Measurement
Bureau
c. Drug Safety Monitoring Board
d. Data and Safety Monitoring Board
D

, In any trial, what should be the main concern of the physician?
A. The welfare of the subjects
b. Ensuring that the allotted quota of
subjects enrolled
c. The esteem that will be gained from a
successful trial outcome
d. The scientific outcome of the trial
A
The World Medical Association (WMA) ethical principles for medical research involving
human
subjects is called:
a. The International Research Act
b. The Belmont Report
c. The National Research Act
d. The Declaration of Helsinki
D
The process by which a subject voluntarily confirms his or her willingness to participate in a
clinical
trial is known as:
a. Intent to treat
b. Legally authorized agreement
c. Informed consent of trial subjects
d. IRB/IEC approval
C
One of the primary purposes of a Phase I study is to:
a. Demonstrate long term safety and efficacy
b. Determine he metabolic and pharmacologic action of the drug in humans
c. Demonstrate efficacy within the established safe dose range
d. Gather information on additional indications for the drug
B
What is the purpose of the 'Data and Safety Monitoring Board (DSMB)'?
A. To approve the trial protocol
b. To ensure that the monitor is performing his/her duties correctly
c. To assess the progress of a clinical trial, the safety data, and the critical efficacy endpoints
d. To ensure the accuracy of data and to carry out data analysis
C
. What does the IRB/IEC evaluate? (select all that apply)
a. The subject-selection procedure

Voordelen van het kopen van samenvattingen bij Stuvia op een rij:

Verzekerd van kwaliteit door reviews

Verzekerd van kwaliteit door reviews

Stuvia-klanten hebben meer dan 700.000 samenvattingen beoordeeld. Zo weet je zeker dat je de beste documenten koopt!

Snel en makkelijk kopen

Snel en makkelijk kopen

Je betaalt supersnel en eenmalig met iDeal, creditcard of Stuvia-tegoed voor de samenvatting. Zonder lidmaatschap.

Focus op de essentie

Focus op de essentie

Samenvattingen worden geschreven voor en door anderen. Daarom zijn de samenvattingen altijd betrouwbaar en actueel. Zo kom je snel tot de kern!

Veelgestelde vragen

Wat krijg ik als ik dit document koop?

Je krijgt een PDF, die direct beschikbaar is na je aankoop. Het gekochte document is altijd, overal en oneindig toegankelijk via je profiel.

Tevredenheidsgarantie: hoe werkt dat?

Onze tevredenheidsgarantie zorgt ervoor dat je altijd een studiedocument vindt dat goed bij je past. Je vult een formulier in en onze klantenservice regelt de rest.

Van wie koop ik deze samenvatting?

Stuvia is een marktplaats, je koop dit document dus niet van ons, maar van verkoper DrBellaPhD. Stuvia faciliteert de betaling aan de verkoper.

Zit ik meteen vast aan een abonnement?

Nee, je koopt alleen deze samenvatting voor €12,17. Je zit daarna nergens aan vast.

Is Stuvia te vertrouwen?

4,6 sterren op Google & Trustpilot (+1000 reviews)

Afgelopen 30 dagen zijn er 64438 samenvattingen verkocht

Opgericht in 2010, al 14 jaar dé plek om samenvattingen te kopen

Start met verkopen
€12,17
  • (1)
  Kopen