25 Questions
Which organization in Canada reviews and approves drug products before they can be sold?
Health Canada
How long does the federal review process for a new drug submission in Canada typically take?
1-2 years
In which phase of investigational drug studies are a larger number of patients followed by medical research centers?
Phase 3
What is the purpose of post-marketing studies conducted by drug companies?
To obtain information on the therapeutic and adverse effects of the new drug
What is a Drug Identification Number (DIN) used for?
To uniquely identify a specific drug product
In which type of studies is the use of placebos considered unethical?
New drug studies
Which piece of legislation is the primary governing body for food, drugs, cosmetics, and medical devices in Canada?
The Canadian Food and Drug Act
Which act replaced the Narcotic Control Act in 1997 and regulates the possession, production, distribution, and sale of controlled substances in Canada?
The Controlled Drugs and Substances Act
What is printed on the label of every narcotic drug in Canada?
Both the letter N and the symbol (c)
What are the steps involved in the approval process for new drugs in Canada?
Chemical and Biological research, Pre-clinical development, Clinical Trials
Which phase of clinical trials comes after Phase 2?
Phase 3
Which act set rules for the manufacture and distribution of drugs considered to have potential for abuse?
The Controlled Drugs and Substances Act
Which of the following is a key consideration for patient transfer within or between facilities or provider teams?
Ensuring the patient has their latest medication list
What should be done to prevent medication errors?
Follow the 10 rights of medication administration
What is the purpose of having two patient identifiers?
To confirm the patient's identity
What should be done before administering medication?
Draw up or prepare the medication yourself
What should be done to minimize verbal or telephone hours when dealing with medication orders?
List the indication next to each order
What is the importance of listing the indication next to each medication order?
To provide clear information about why the medication is prescribed
What should be done if you did not draw up or prepare the medication yourself?
Do not administer the medication
Which of the following is NOT a right that patients must be informed of during the informed consent process?
The right to leave the study with no consequences to medical care
Which legislation regulates nurses' actions when providing care, including medication administration?
Regulated Health Professions Act
Which of the following is considered a controlled act in the context of administering medication?
Administering a substance by injection
Which of the following is NOT one of the nursing practice standards of care?
Maintaining privacy and confidentiality
What are the three principles that outline the expectations related to medication practices that promote public protection?
Authority, Competence, Safety
What are the Ten Rights of medication administration?
Right drug, Right dose, Right time, Right route, Right patient, Right reason, Right documentation, Right evaluation, Right patient education, Right to refuse
Test your knowledge on the informed consent process and patients' rights in healthcare. Learn about the importance of providing complete information, alternative options, and the ability to leave a study without consequences. Explore legislation and regulations related to nursing and healthcare practices.
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