The College of Pharmacists of Manitoba (formerly known as the “Manitoba Pharmaceutical Association”) continues to adapt the content on www.cphm.ca in order to reflect the December 2006 Pharmaceutical Act , implemented January 1, 2014. The documents on the website with “Manitoba Pharmaceutical Association” or “MPhA” have not been updated and may not be consistent with the current legislation. Questions on this content can be directed to the College office.
Legislation and Supporting Documents
Orientation to the New Practice Framework (updated January 19, 2014 )
This manual was developed to help answer questions around the new Act, July 2013 Regulations
and practice directions implemented January 1, 2014.
December 2006 the Pharmaceutical Act (posted January 3, 2014)
Manitoba Pharmaceutical Regulation (July 2013) (posted January 3, 2014) - NOTE: Government to amalgamate with Pharmaceutical Regulation, amendment (see next item)
Manitoba Pharmaceutical Regulation, amendment (posted September 30, 2016) - NOTE: Government to amalgamate with Pharmaceutical Regulation (see item above)
Code of Ethics (January 1, 2014)
The Code of Ethics governs the conduct of members, students, interns and owners.
- Code of Ethics - Explanatory Document (posted February 26, 2014)
Clinical & Physician Assistants
Clinical & Physician Assistant: Prescribing Authority (updated November 2016)
For a list of Clinical and Physician Assistants, please click here.
For an updated list of Dentists, please click here. [To be updated]
For the Physician Directory, Currently Licensed and Practising in the Province please click here .
Registered Nurses (Extended Practice)
For a list of Veterinarians, please click here.
A practice direction is a written statement made by Council for the purpose of giving direction to members and owners about the conduct of their practice and pharmacy operations. Compliance with approved practice directions is required under The Pharmaceutical Act .
Practice Directions Policy Statement
National Association of Pharmacy Regulatory Authorities (NAPRA) Model Standards
NAPRA Supplemental Standards of Practice for Shedule II and III Drugs
NAPRA Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations*
NAPRA Model Standards for Pharmacy Compounding of Hazardous Sterile Preparations *
*For more information on the current compounding guidelines and the implementation schedule and deadlines for Manitoba compounding pharmacies for the NAPRA Model Standards for Pharmacy Compounding of Non-Hazardous and Hazardous Sterile Preparations, please the the following section titled 'Pharmacy Compounding.'
The current standards for pharmacy compounding in Manitoba are as follows:
- Guidelines on Sterile Production in Pharmacies and Handling and Disposal of Hazardous Pharmaceuticals
With a stepwise approach, the College will replace the Extemporaneous Compounding Guideline and the Guidelines on Sterile Production in Pharmacies and Handling and Disposal of Hazardous Pharmaceuticals with a suite of model pharmacy compounding standards developed by the National Association of Pharmacy Regulatory Authorities (NAPRA). Please see the following section for more information.
NAPRA Model Standards for Pharmacy Compounding of Non-Hazardous and Hazardous Sterile Preparations
On February 6, 2017, College Council approved an implementation schedule for the NAPRA Standards for Pharmacy Compounding of Non-hazardous and Hazardous Sterile Preparations with the following motion:
Council approved a phased-in implementation schedule, with the first implementation requirement date of June 1, 2018, with the expectation for total compliance throughout Manitoba by January 1, 2021, for the NAPRA Model Standards for the Compounding of Non-Hazardous Sterile Preparations and the Compounding of Hazardous Sterile Preparations.
To review the NAPRA model standards for pharmacy compounding, please visit the following links:
All pharmacies engaged in non-hazardous and/or hazardous sterile preparation are required to transition to the NAPRA Model Standards according to the implementation schedules below:
The third and final Model Standards document for Non Sterile Compounding is expected to be released by early 2018.
In 2011, Council made the decision to accept the then current Standards of Practice documents as practice directions under the new legislation in order for the Standards of Practice Committee to focus on the creation of new practice directions that were needed under the new regulations and expanded scope of practice for pharmacists. The Standards of Practice listed below are now considered "practice directions" and will be reviewed by the Standards of Practice Committee in due course.
Community Standards of Practice [practice direction]
Hospital Standards of Practice and Guidelines [practice direction]
Personal Care Home - Long-Term Care Standards of Practice [practice direction]
After a series of Special General Meetings and opportunities for member feedback, as per the Practice Directions Policy Statement, the following practice directions have been approved by Council.
Adaptation of a Prescription [effective January 1, 2014]
Practice Aid: Adaptation [posted January 23, 2015]
Administration of Drugs including Vaccines [Standard of Practice #5 [updated and posted June 25, 2014]
Advertising in Manitoba Pharmacies [effective February 8, 2016]
Alternate Verification Program: Drug Packaging [effective April 24, 2015]
Central Fill [effective April 11, 2014]
Clinical Practice Pharmacies Practice Direction [effective October 5, 2015]
Delegation of Dispensing to Other Health Professionals Practice Direction [effective December 18, 2015]
Drug Distribution Practice Direction [effective July 8, 2016]
Ensuring Patient Safety [updated document is effective March 13, 2015]
Exempted Codeine Practice Direction [effective February 1, 2016]
Aids to the Exempted Codeine Practice Direction:
Incidents and Discrepancies Practice Direction [effective July 8, 2016]
Lock and Leave Component [effective January 1, 2014]
Manitoba Prescribing Practices Program (M3P) Information Entered into DPIN [effective January 1, 2014]
Pharmacy Facilities [Standard of Practice #15] [effective January 1, 2014]
Patient Counselling [effective October 10, 2014]
Patient Profiles [effective October 10, 2014]
Permanent and Temporary Pharmacy Closure [effective July 4, 2014]
Prescribing [amended October 6, 2014]
Prescribing and Dispensing [Standard of Practice #4] [effective January 1, 2014]
Records and Information [Standard of Practice #12] [effective January 1, 2014]
Referring a Patient
Refill History Recording System [effective February 13, 2015]
Sale of Schedule 2 Drugs [effective January 1, 2014]
Sale of Schedule 3 Drugs [effective January 1, 2014]
Secondary Hospital Services Component Practice Direction [effective December 18, 2015]
Termination of Patient Relationship [Standard of Practice #11] [effective July 4, 2014]
Test Interpretation [Standard of Practice #7] [effective January 1, 2014]
Transfer of Patient care [Standard of Practice #10] [effective January 1, 2014]
Supervision [effective July 4, 2014]
*This practice direction serves as a guideline for pharmacy managers considering submission of a proposal for Council approval to implement an Alternate Verification Program in their pharmacy. Please be advised that pharmacy managers must receive prior approval by Council of their proposal before an Alternate Verification Program can be initiated in their pharmacy.
A Practice Direction is a written statement made by Council for the purposes of giving direction to members and owners about the conduct of their practice and pharmacy operations. Before a Practice Direction is approved by Council, members are provided with the opportunity to review and provide their feedback on draft practice directions, for consideration at Council. Compliance with approved Practice Directions is required under The Pharmaceutical Act .
There are no Practice Directions currently open for member feedback.
On April 25, 2014, Council passed a motion to accept the document’s proposed requirements for the PPMS used by pharmacy professionals for compliance in Manitoba pharmacies by January 1, 2016, in conjunction with NAPRA’s effective date. The following guidelines are approved by Council. They are policies and practice indicators developed under the old legislation and are still valid under the new legislation. These documents will be reviewed by Council in due course.
Adverse Drug Reaction Guidelines
Guidelines for Pharmacists Dispensing Mifegymiso in Manitoba
Guidelines for pharmacy licence holders wanting to use more than one name for their pharmacy
Guidelines on sterile production in pharmacies, and handling and disposal of hazardous pharmaceuticals
Narcotic and Controlled Drug Accountability Guidelines
Needle Stick Injury Guideline (added June 30, 2015)
Procedures in the Event of a Robbery or Burglary [updated December 2014]
Satellite Pharmacy Component Criteria
Self-Testing Product Guidelines
Practice Direction for Advertising*
* Requested by Council to be revised and transitioned by the Standards of Practice Committee with consultation by the members and stakeholders. Consultation has closed and Council has referred feedback received on this practice direction consultation to the Standards of Practice Committee for further review and consideration and asked the Registrar to provide additional information for the consideration of the Committee.
Opioid Replacement Therapy Guidelines for Manitoba Pharmacists
The Opioid Replacement Therapy Guidelines for Manitoba Pharmacists (ORT Guidelines) replaces the Principles for the Provision of Opioid Dependence Treatment by Manitoba Pharmacists guideline document .
ORT Guidelines is a new title that corresponds with the interprofessional Opioid Replacement Therapy 101 workshop which is required education for at least one pharmacist at each pharmacy that is dispensing methadone or buprenorphine. Other changes include:
- More comprehensive drug information and updated education requirements on buprenorphine/naloxone as the use of this medication has increased with new provincial drug coverage
- Updated information from Provincial Drug Programs for methadone reimbursement procedures
At least one pharmacist within a pharmacy dispensing methadone and/or buprenorphine must be extensively knowledgeable and the expectation is that the “Opioid Replacement Therapy 101: An introduction to clinical practice” course is successfully completed within 6 months of initiating care. The pharmacist with specialized training at a pharmacy is responsible for training all pharmacists who will be dispensing methadone and/or buprenorphine. It is strongly recommended that pharmacists dispensing methadone and/or buprenorphine/naloxone also complete the theoretical training, “Opioid Replacement Therapy 101: An introduction to clinical practice”, to gain additional insight on the interprofessional collaborative approach to opioid replacement therapy. All pharmacists providing ORT services must review the Opioid Replacement Therapy Guidelines for Manitoba Pharmacists.
All pharmacists who have patients at their pharmacy on buprenorphine/naloxone or buprenorphine must complete the free six-hour professional development program available online at www.suboxone.ca
If you are interested in taking an Opioid Replacement Therapy workshop, please contact Karen Sorenson at The College of Physician and Surgeons of Manitoba by email: firstname.lastname@example.org .
Additional recommended readings for pharmacists dispensing opioid replacement therapy include:
- College of Physicians and Surgeons of Manitoba (CSPM) Methadone & Buprenorphine Maintenance – Recommended Practice
- Opioid Agonist Maintenance Treatment: A pharmacist’s guide to methadone and buprenorphine for opioid use disorder
For additional resources on dispensing and administering naloxone please review the section below.
Manitoba, along with the rest of Canada, has seen a rise in the number of opioid overdose deaths in recent years. As a result, some pharmacies in the province have begun selling naloxone kits and providing education to people and organizations in need of this life-saving drug that can temporarily reverse the effects of an overdose.
The College encourages all pharmacies to carry naloxone kits to support the province-wide effort to address the opioid crisis. Pharmacies selling naloxone must comply with the Guidelines for Pharmacists Selling Naloxone as a Schedule II Drug (Guidelines).
Please review the Guidelines for more information about selling naloxone, including:
Relevant practice directions
If your pharmacy carries naloxone kits and you would like to be added to the publically available College listing of Pharmacies Carrying Naloxone Kits , please email your pharmacy's name, address, and telephone number to Rachel Carlson, Communications Coordinator, at email@example.com .
For additional information and resources on opioid overdose and naloxone, please see the resources below:
College of Pharmacists of Manitoba Resources*:
Naloxone Listing - College of Pharmacists of Manitoba
College of Pharmacists of Manitoba Checklist for Naloxone Injection Training
College of Pharmacists of Manitoba Checklist for Naloxone Nasal Spray
Naloxone Brochure for Ampoules (black and white)
Naloxone Brochure for Ampoules (colour)
College of Pharmacists of Manitoba Naloxone FAQ
University of Waterloo, School of Pharmacy Resources
Naloxone Administration (by injection) (video)
Naloxone Administration (by nasal spray) (video)
5 Things to Know About Naloxone (video)
Manitoba Addictions and Knowledge Exchange: Fentanyl - Information and Resources
*The Naloxone educational information included above was developed through a partnership between the College of Pharmacists of BC, the BC Centre of Disease Control and the Province of BC's Ministry of Health.
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License .
The naloxone educational resources above are available under the Creative Commons Attribution-ShareAlike License to use and remix as needed to help provide patients and pharmacy professionals with important information on the use of this life saving drug.
Manitoba Prescribing Practices Program (M3P)
Manitoba Prescribing Practices Program (M3P Information Entered into DPIN Practice Direction
M3P Questions and Answers [updated August, 2016]
List of Drugs Covered by the Multiple Prescription Program
Regulations Governing the Multiple Prescription Program
Prescriptions from other Provinces
Newsletter Items Relating to M3P
M3P DPIN Entry Information
Permanent and Temporary Pharmacy Closure [effective July 4, 2014]
New Pharmacy Opening Package [for 2016]
Procedures in the Event of a Robbery or Burglary
Prescription Forgeries [from the Summer 2013 Newsletter]
PHIA Pledge of Confidentiality
Distance Care IPS Disclaimer
Manitoba Medications Return Program Website
Manitoba Medication Return Program FAQ [updated November 3, 2014]
Frequently Asked Questions: Patient Record Destruction
Healthcare professionals from various disciplines, including pharmacy, are often jointly involved in the care of a common patient even though individual professionals are not in direct contact with one another. Joint statements are developed between healthcare professions to maintain patient safety and ensure collaborative patient care.
Prescribing Practices: Doctor/Pharmacist Relationships (updated to reflect the requirement for retention of records for five years)
Electronic Transmission of Prescriptions
Facsimile Transmission of Prescriptions
Facsimile Transmission of Prescriptions Template (pdf template)
Facsimile Transmission of Prescriptions Template (word template)
Q and A: Electronic and Facsimile Transmission of Prescriptions