Jurisprudence Examination (Je) Information Guide: 5029-Reginfo - Je V2015.6.Docx Revised July 30, 2015

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JURISPRUDENCE EXAMINATION (JE) INFORMATION GUIDE

A.
B.
C.
D.
E.
F.
G.
H.
I.
J.
K.
L.

General information
Study Information
Examination dates
Eligibility/application procedure
Out-of-Vancouver sitting of examination
Examination Accommodation
Withdrawal/refund policy
Scoring and results
Appeals
Examination day process and security of materials
Examination format and blueprint
Appendices

A. General Information
The Jurisprudence Examination (JE) is based on legislation contained in federal and provincial acts, their
regulations, bylaws and published College Professional Practice Policies that pertain to pharmacy
operations and registrant (pharmacist or pharmacy technician) responsibilities in the practice of
pharmacy. The examination is designed to assess the applicants knowledge of and ability to interpret
and apply all legislation that impacts on current pharmacy practice in B.C. It is not intended that
applicants memorize the drug schedules, but they should be prepared to identify, interpret, and apply
the pertinent legal requirements and procedures to be followed. Drug schedules will be supplied at the
examination.
All applicants must read and adhere to Registration Committee Policy-3 Jurisprudence Examination. As
stated in this policy, an applicant may write the JE a maximum of 4 times.
B. Study Information
For information on what to study for the exam, see the following JE Orientation Presentation:
JE Orientation Presentation (mp4)
JE Orientation Presentation (mp3)
The examination is based on information in the Colleges BC Pharmacy Practice Manual available at:
http://www.bcpharmacists.org/bc-pharmacy-practice-manual-0.

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Refer to the Appendices below for the specific sections of legislation covered on the examination.
Applicants are encouraged to use the College website as the primary and most current source of
information about pharmacy legislation, standards of practice and policies. Those unable to access
website resources may place an order through eServices -> Online Store to purchase a BC Pharmacy
Practice Manual.
Note that pharmacists and pharmacy technicians are referred to as registrants in the new Acts and
Bylaws. The term registrant is used in all examinations.
C. Examination Dates
For 2015 only, there will be four JE sittings held in February, June, September, and November.
For all other years, JE sittings are held three times a year in February, June and October. Registration for
each sitting will be made available approximately 2 to 3 months prior to the date of the exam.
For upcoming JE dates, refer to the Registration section of the College website or log into eServices.
D. Eligibility/Application Procedure
To be eligible to register for the JE, you must be

pre-registered with the College, or

a UBC student in the final year of their pharmacy program.


To allow sufficient time for processing, the pre-registration application, along with all required
documentation, should be received at least one month prior to the JE registration deadline.
Once applicants have pre-registered, they will receive an eServices ID number which can be used for
online exam registration.
Registration for all exam sittings must be completed online through eServices on the College website
and pay the applicable fees.
Once registered for the exam, applicants will receive a payment confirmation email. To view details of
the exam registered for (e.g. exam location, date, and time), log into eServices -> Register for Events.
Applicants must bring picture identification.
E. Outside-of-Vancouver Sitting of Examination
Various locations throughout Canada have been pre-selected for those who wish to write the JE outside
of Vancouver. The site and invigilator will be determined by the College and the exact time and location
of the exam sitting will be available online at the time of exam registration. To view details of the exam
and to register, log into eServices -> Register for Events.
Applicants must adhere to Registration Committee Policy-3 Jurisprudence Examination.

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F. Examination Accommodation
Applicants should refer to Registration Committee Policy-4 Examination Accommodation Policy if they
wish to make a request for testing accommodations. A written request for the accommodation must be
made at least 4 weeks prior to the examination date.
G. Withdrawal/Refund Policy
The fee for the examination is non-refundable and non-transferable to a different location or a future
examination sitting. Special consideration may be given for medical reasons (physicians note is
required) and bereavement reasons. In these cases, a written request must be submitted to the College
and is subject to an administration fee.
H. Scoring and Results
Each question on the exam is worth one point. The full examination is weighted by the significance of
the question in each category with respect to pharmacy practice. The pass/fail standard for the JE is
established for each exam using a standard setting process. A representative group of registrant experts
conduct a thorough review of the content of the examination, determining the minimum number of
questions that must be answered correctly on that examination in order to pass. The ability level that
corresponds to that minimum passing score is the pass/fail standard for the JE.
Applicants will be advised of their exam results one month after the scheduled exam date. Applicants
will be issued a standard met or standard not met result; actual scores will not be issued. For reasons
of confidentiality, results will not be released by telephone, fax, or email. There will be no exceptions.
Jurisprudence Examination results are valid for a period of three years from the date the examination
was written.
I. Appeals
Appeals for the Jurisprudence exam will only be considered for procedural incidents or personal
circumstances that may have affected an applicants performance on the exam. Refer to Registration
Committee Policy-3 for Jurisprudence Examination.
J. Examination Day Process and Security of Materials
Admission and Identification:
1. All applicants must show valid photo-identification (drivers license, passport, permanent resident
card, UBC student card) and sign the registration list.
2. Applicants will place their personal belongings at the front or back of the room or as instructed by
the invigilator, prior to the commencement of the examination and until the examination is
complete.

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3. No applicant shall be permitted to enter the examination room after the first 30 minutes or to leave
during the first 30 minutes of the examination. Applicants who choose to enter once the
examination has begun and within the first 30 minutes of the exam, will not be given any additional
time to write the examination.
4. Applicants may bring a snack packaged in a clear plastic bag and water in a clear bottle with labels
removed.
Applicant Materials/Conduct:
1. The examination consists of a specific number of pages. Applicants must ensure they have received
a complete examination paper. Applicants must read, print their name and sign the examination
cover sheet. In signing the examination paper, applicants agree to maintain the confidentiality of all
questions contained in the examination paper.
2. During the examination, the only material that may be consulted in answering questions is the drug
schedules provided with the examination paper. No other reference material is permitted.
3. A copy of the drug schedules without the explanatory/descriptive information will be provided.
Applicants are responsible to know how to use all of the schedules. A copy of the prescription
regulations chart will not be provided. See Appendix A.
4. Applicants must not bring with them any electronic device including calculators, pagers, cellular
phones and/or personal digital assistants (PDAs).
5. All procedures including filling in answers on the exam answer sheet must be completed within the
three hour time allotment. The examination is scored based on the answers on the exam answer
sheet only. An HB or preferably a #2B lead pencil must be used to mark the answer sheet.
Applicants are responsible for bringing a pencil and eraser to the examination.
6. Applicants will not be permitted to ask questions of the invigilator except in cases of supposed
errors in the papers.
7. Time will be called out when there is 2 hours, 1 hour, hour and 15 minutes remaining in the
examination.
8. Applicants found performing any of the following or similar dishonest practices shall be immediately
dismissed from the examination, and the matter shall be reported to the Registration Committee.
a.
Using any books, papers, or other materials other than those provided by the College.
b.
Communicating with other applicants under any circumstances whatsoever during the
examination period.
c.
Exposing written papers to the view of other applicants.
d.
Cheating on the exam.
e.
Impersonating an examination applicant.
f.
Threatening or belligerent behavior to others.

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9. Applicants who need to leave the examination for any reason must be escorted by an invigilator,
one applicant at a time.
Sign-Out Procedure
1. No applicant shall be permitted to leave during the first 30 minutes of the examination.
2. Applicants are not permitted to leave the examination room in the last 15 minutes of the
examination. Applicants remaining during the last 15 minutes of the examination must remain
seated until the end of the examination period and then proceed to sign-out.
3. Applicants must return the entire examination paper, drug schedules and exam answer sheet to the
invigilator.
4. Applicants must sign-out upon completion of the examination.
K. Examination Format & Blueprint
The JE is a 3-hour examination composed of 150 questions, including multiple choice and true or false.
The following represents the major question categories on the Jurisprudence Examination and their
approximate weightings (proportion of questions on the examination related to that component).
Categories

Percent of Questions

Health Professions Act, Pharmacy Operations and Drug Scheduling Act


Bylaws related to pharmacy practice, professional practice policies
Food and Drugs Act, Regulations and Schedules, Controlled Drugs and Substances
Act, Regulations and Schedules, BC Drug Schedules

15
45
40

Types of Questions
Multiple Choice
On the scannable answer sheet, fill in the circle that corresponds to the same letter as the correct
answer on the examination paper. Ensure that the question numbers on the answer sheet correspond
with the question number on the examination paper.
1. Verbal prescription narcotics may be dispensed on the verbal instructions of:

A.
B.

a physicians nurse
an intern

C. a practitioner
D. all of the above

E. (B) and (C) are correct

Answer: C

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2. Indicate the requirements for sale of 60 Ranitidine 150mg.

A.
B.

Prescription required
Professional Service Area sale

C. Professional Product Area sale


D. Drug product which may be sold from any retail
outlet

Answer: C
3. Indicate the requirements for sale of Heparin Topical.

A.
B.

Prescription required
Professional Service Area sale

C. Professional Product Area sale


D. Drug product which may be sold from any retail
outlet

Answer: C
On the answer sheet find the answer circles for questions 1-3, and fill the circle containing the letter C.
True-False
On the answer sheet fill in the appropriate answer circle ensuring that the question number on the
answer sheet corresponds correctly with the question number on the examination paper.
4. Schedule II drugs may be sold without a prescription from any retail outlet.

A.
B.

True
False

The correct answer to question 4 is B. On the answer sheet, find the answer circles for question 4, and
fill the circle containing the letter B.

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L. Appendices
Appendix A Jurisprudence Examination Content
1. Federal legislation
a. Food and Drugs Act Regulations (http://lawslois.justice.gc.ca/eng/regulations/C.R.C.,_c._870/). The relevant extracts include:
PART C: DRUGS sections C.01.041 - C.01.049.
PART G: CONTROLLED DRUGS
o DIVISION 1: GENERAL sections G.01.001 - G.01.007.
o DIVISION 3: PHARMACISTS sections G.03.001 - G.03.017.5.
o DIVISION 4: PRACTITIONERS sections G.04.001 - G.04.004.5.
o DIVISION 5: HOSPITALS sections G.05.001 - G.05.004.
o DRUG SCHEDULE TO PART G Part I, Part II, Part III (these drug schedules
will be supplied for the Jurisprudence Examination)
Prescription Drug List (http://www.hc-sc.gc.ca/dhp-mps/prodpharma/pdlord/pdl_list_fin_ord-eng.php)
b. Controlled Drugs and Substances Act, Schedule and Regulations (http://lawslois.justice.gc.ca/eng/acts/C-38.8/index.html). The relevant extracts include:
i. Narcotic Control Regulations
(http://laws-lois.justice.gc.ca/eng/regulations/C.R.C.,_c._1041/index.html)
o Interpretation section 2
o Pharmacists section 30 - 52
o Practitioners section 53 - 54
o Hospitals section 63 - 65
o General section 70 - 71
o Narcotic Drug Schedules (these drug schedules will be supplied for the
Jurisprudence Examination)
ii. Benzodiazepines and other Targeted Substances Extracts (http://lawslois.justice.gc.ca/eng/regulations/SOR-2000-217/index.html)
o
o
o
o

Section 2(1) 2(3), 3(a), 3(b)(i-ii), 5 - 7


Part 2 - Pharmacists section 48 - 57
Part 4 - Hospital section 63 - 67
Schedule 2 (this will be included in the drug schedules supplied for the
Jurisprudence Examination)

2. Provincial legislation
a. The Health Professions Act (HPA sections 15.1, 16, 17, 25.8 - 25.95, 32.2), HPA Bylaw
sections 64-83, HPA Bylaw Schedule F (Part 1 and 3), the Pharmacy Operations and Drug
Scheduling Act (PODSA), PODSA Bylaws, drug schedules and drug schedule definitions. (HPA
Bylaws, sections 2-63 is not tested on the Jurisprudence Exam.)

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b.

c.

d.
e.
f.
g.
h.
i.

j.
k.

l.

Code of Ethics practice oriented questions relating to the Code of Ethics.


http://www.bcpharmacists.org/library/D-Legislation_Standards/D2_Provincial_Legislation/5019-Code_of_Ethics_Detailed.pdf
(Note: you do not need to memorize the Code of Ethics).
Professional Practice Policies (on the College website at:
http://www.bcpharmacists.org/library/A-About_Us/A-2_Governance/5003-PGP-PPP.pdf)
and the Amendment to the Professional Practice Policy #58 (on the College website at:
http://www.bcpharmacists.org/library/D-Legislation_Standards/D2_Provincial_Legislation/PPP58_AmendmentOrientationGuide.pdf)
Controlled Prescription Program.
Prescription Regulations Chart.
Recent legislation information from the ReadLinks and College mailings.
http://www.bcpharmacists.org/resources/readlinks.php
Facsimile transmission of prescriptions (HPA Bylaws, Schedule F, Part 1 Community
Pharmacy Standards of Practice, Section 7)
Responsibilities of pharmacy managers (PODSA Bylaws, Section 3).
Pharmacy Technician scope of practice and Pharmacists responsibilities and pharmacy
assistants functions (HPA Bylaws, Schedule F, Part 1 Community Pharmacy Standards of
Practice, Section 4 and 5).
Operation without a pharmacist (PODSA Bylaws, Section 12).
NAPRA Professional Competencies for Canadian Pharmacy Technicians at Entry to Practice
http://www.napra.org/Content_Files/Files/Professional_Competencies_for_Canadian_Phar
macy_Technicians2007.pdf
All information related to pharmacy practice.

3. Drug Schedule resource provided for the Jurisprudence Exam:


Consolidated copy, or
Individual links:
o CPBC (provincial) Drug Schedules Regulation without the
explanatory/descriptive information http://library.bcpharmacists.org/DLegislation_Standards/D-4_Drug_Distribution/5012Drug_Schedules_Regulation.pdf
o Definition of drugs on the Prescription Drug List (formerly Schedule F drugs)
o Controlled Drug and Substances Act
Schedule I http://laws-lois.justice.gc.ca/eng/acts/C-38.8/page24.html#h-28
Schedule II http://laws-lois.justice.gc.ca/eng/acts/C-38.8/page25.html#h-29
o Benzodiazepines and Other Targeted Substances Regulations
Schedule 2 http://laws-lois.justice.gc.ca/eng/regulations/SOR-2000217/page-29.html#docCont
o Food and Drug Regulations Schedule Part I III http://lawslois.justice.gc.ca/eng/regulations/C.R.C.%2C_c._870/page-350.html#docCont

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Appendix B Other Examination Information


1. Food and Drug Regulations, Prescription Drug List (formerly Schedule F) includes all prescription
drugs available for sale in Canada except for narcotic, controlled, and targeted drugs. It is divided
into two parts. Part 1 includes regular prescription drugs for human use which are neither narcotic,
controlled or targeted drugs. Part 2 includes drugs for veterinary use.
2. A drug on the Prescription Drug List under the Food and Drug Regulations that is a prescription may
be included under a different name or therapeutic classification in the British Columbia drug
schedules. For example: estrogen and progesterone are included under Sex Hormones; warfarin is
included under 4-hydroxycoumarin; prednisone is included under Adrenocortical Hormones.
3. The definition of a practitioner is not included in the Extracts to the Food and Drug Regulations. A
practitioner for the prescriptive authority of drugs on the Prescription Drug List (Schedule 1 drugs)
includes medical physicians, dentists, podiatrists, veterinarians, nurse practitioners, optometrists,
and naturopathic physicians.
4. The definition of a practitioner under the Controlled Drugs and Substances Act (CDSA) (page one of
the Extracts to the Narcotic Control Regulations) includes a person authorized to practice medicine,
dentistry, and veterinary medicine. Podiatrists are allowed to prescribe benzodiazepines.
5. The Extracts to the Food and Drug Regulations and the Extracts to the Narcotic Control Regulations,
state that prescriptions and any records must be retained for a period of two years. The PODSA
Bylaws, Section 8(1) state that prescriptions and patient records must be retained for three years
from the date of the last refill. B.C. provincial legislation overrides the federal legislation, as it is
more stringent. Invoices recording the purchase and receipt of Schedule 1 drugs and drugs regulated
by the Controlled Drugs and Substances Act and any records documenting the transfer of such drugs
for any reason other than as authorized by a practitioners prescription must be retained for not less
than three years.
6. The PODSA definition of a practitioner only applies to those drugs listed in our schedules that are
not narcotic, controlled drugs, or those drugs included in the Controlled Prescription Program.
Podiatrists may prescribe benzodiazepines but not the other target drugs.
7. The definition of Control Drugs Part 1, Part 2 and Part 3 is best described in the Prescription
Regulations Synopsis.
Controlled Drug Part 1 = reportable control drugs
Controlled Drug Part 2 = non-reportable control drugs
Controlled Drug Part 3 = non-reportable anabolic steroids
8. Frequently asked questions:
Targeted drugs: Part 1:
Targeted drugs: Part 2:
Narcotic and controlled drugs:

Drugs which may be sold (benzodiazepines and others)


Drugs which may not be sold as they are illegal to possess
Narcotic Part 1 = reportable narcotics
Narcotics Part 2 = non-reportable narcotics

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9. A non-prescription drug not listed in Schedule 2 or Schedule 3 of the British Columbia drug
schedules, means that it is unscheduled and can be placed outside the 25-foot perimeter of the
pharmacy or be sold from non-pharmacy outlets. Unscheduled drugs are not listed in the British
Columbia drug schedules. For example, chlorpheniramine.
10. In British Columbia a prescription with authorized ongoing refills is only valid for one year from the
prescribing date of the original prescription. The only exception is prescriptions for oral
contraceptives, for which the pharmacists shall restrict the time span for ongoing prescription
authorization to a maximum of two years from the prescribing date (HPA Bylaws, Schedule F, Part 1,
Community Pharmacy Standards of Practice, Section 10(5).
11. Veterinary drugs cannot be sold without a prescription from a veterinarian unless they are sold only
in the manufacturers original container labeled for veterinary use only or for agricultural use
only. The pharmacist cannot repackage veterinary drugs to be sold without a prescription.

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