Fees for Health Canada
List of current Health Canada fees. For additional information please visit the program webpages.
On this page
- Drugs (human and veterinary)
- Fees for the examination of a submission - drugs for human use
- Fees for examination of a submission - drugs for veterinary use only
- Fees for right to sell drugs
- Drug establishment licence fees - drugs for human and veterinary use
- Drug establishment licence fees - dealer's licences
- Certificate of supplementary protection application fees
- Certificate of pharmaceutical product fees
- Master file fees
- Biocides
- Medical devices
- Pesticides
- Hazardous materials
- Cannabis
- Tobacco
- National dosimetry services
Drugs (human and veterinary)
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| New active substance | 606,286 | 616,593 |
| Clinical or non-clinical data and chemistry and manufacturing data | 313,944 | 319,282 |
| Clinical or non-clinical data only | 125,533 | 127,668 |
| Comparative studies | 70,750 | 71,953 |
| Chemistry and manufacturing data only | 43,529 | 44,269 |
| Clinical or non-clinical data only, in support of safety upgrades to the labelling | 22,977 | 23,368 |
| Labelling only | 6,328 | 6,436 |
| Labelling only (generic drugs) | 2,378 | 2,419 |
| Administrative submission | 1,002 | 1,020 |
| Disinfectant - Full review | 13,186 | 13,411 |
| Labelling only (disinfectants) | 2,964 | 3,015 |
| Drug identification number application - Labelling standards | 1,912 | 1,945 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Application for drug identification number - Information, other than that referred to in item 2, to support an application for a number, including the submission of labelling material for a second review, if required | 2,606 | 2,946 |
| Application for drug identification number - Published references or other data | 1,812 | 2,047 |
| Application for drug identification number - Documentation to support a change of manufacturer, a change to the name of a manufacturer or a change to the brand name of a drug | 906 | 1,025 |
| Notification - Veterinary health product - Information contained in a notification filed under subsection C.01.615(1) of the Food and Drug Regulations in respect of a veterinary health product | 578 | 588 |
| New Drug Submission - Efficacy and safety data (in the intended species) to support a single route of administration, dosage form and indication in one animal species. (In the case of an antiparasitic drug, several indications in one food animal species.) | 57,787 | 65,297 |
| New Drug Submission - Efficacy and safety data (in the intended species) to support a single route of administration and dosage form for an antiparasitic drug in one non-food animal species | 35,006 | 39,557 |
| New Drug Submission - Efficacy and safety data (in the intended species) to support a single route of administration, dosage form and indication in two animal species, or a single route of administration, dosage form and two indications in one animal species | 84,038 | 94,961 |
| New Drug Submission - Efficacy and safety data (in the intended species) to support a growth promotion or production enhancement indication in one animal species | 113,795 | 128,589 |
| New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support an additional route of administration | 10,491 | 11,855 |
| New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support each additional strength | 1,739 | 1,964 |
| New Drug Submission - For food-producing animals, toxicity, metabolism and residue depletion studies to establish an acceptable daily intake with a safety factor of 1,000, a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in one species | 78,793 | 89,035 |
| New Drug Submission - For food-producing animals, toxicity, metabolism and residue depletion studies to establish an acceptable daily intake with a safety factor of less than 1,000, a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in one species | 105,044 | 118,700 |
| New Drug Submission - For food-producing animals, residue depletion studies to establish a withdrawal period for an additional dosage form, dosage or route of administration | 10,491 | 11,855 |
| New Drug Submission - For food-producing animals (once an acceptable daily intake with a safety factor of 1,000 or less has been established), metabolism and residue depletion studies to establish a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in an additional species | 52,506 | 59,332 |
| New Drug Submission - Chemistry and manufacturing data for a non-compendial medicinal ingredient of a drug | 17,505 | 19,780 |
| New Drug Submission - Chemistry and manufacturing data to support one strength of a single dosage form | 17,505 | 19,780 |
| New Drug Submission - Chemistry and manufacturing data to support an additional strength of a single dosage form submitted at the same time as item 16 | 8,756 | 9,893 |
| New Drug Submission - Documentation to support a change of manufacturer | 906 | 1,025 |
| Supplement to a New Drug Submission - Efficacy data to support an additional indication in one animal species | 45,528 | 51,445 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support a single route of administration and dosage form for an antiparasitic drug in one non-food animal species | 35,006 | 39,557 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support an indication in another animal species | 57,787 | 65,297 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support a single route of administration, dosage form and indication in two animal species, or a single route of administration and dosage form and two indications in one animal species | 84,038 | 94,961 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support a growth promotion or production enhancement indication in one animal species | 113,795 | 128,589 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support the concurrent use of two drugs approved for the same animal species | 27,990 | 31,628 |
| Supplement to a New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support an additional route of administration | 10,491 | 11,855 |
| Supplement to a New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support each additional strength | 1,739 | 1,964 |
| Supplement to a New Drug Submission - For food-producing animals, residue depletion studies to establish a new withdrawal period for a change in the dosage or route of administration of an approved dosage form in one species | 10,491 | 11,855 |
| Supplement to a New Drug Submission - For food-producing animals, metabolism and residue depletion studies to establish a maximum residue limit and a withdrawal period for a single dosage and route of administration of an approved dosage form in an additional species | 52,506 | 59,332 |
| Supplement to a New Drug Submission - For food-producing animals, toxicity studies to support a change of an established acceptable daily intake, maximum residue limit and withdrawal period | 26,254 | 29,667 |
| Supplement to a New Drug Submission - For the concurrent use of two drugs in a species of food-producing animals, residue depletion studies to determine if an extension to existing withdrawal periods is required | 21,013 | 23,744 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in the source of a medicinal ingredient or its manufacturing process | 17,505 | 19,780 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in formulation or dosage form | 8,756 | 9,893 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in packaging or in the sterilization process | 6,982 | 7,888 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support an extension of the expiry dating | 5,246 | 5,930 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support the concurrent use of two drugs | 5,246 | 5,930 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in the manufacturing site for parenteral dosage forms | 1,739 | 1,964 |
| Supplement to a New Drug Submission - Documentation to support a change to the name of a manufacturer or the brand name of a drug | 906 | 1,025 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support a single route of administration and dosage form | 10,491 | 11,855 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - For food-producing animals, residue depletion studies to confirm that the withdrawal period(s) for each species falls within the conditions of use for the Canadian reference product | 10,491 | 11,855 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - Chemistry and manufacturing data for a non-compendial medicinal ingredient of a drug | 17,505 | 19,780 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - Chemistry and manufacturing data to support a single dosage form | 17,505 | 19,780 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - Documentation to support (a) a change of manufacturer, in the case of an abbreviated new drug submission; or (b) a change to the name of a manufacturer or the brand name of a drug, in the case of a supplement to an abbreviated new drug submission. | 906 | 1,025 |
| Preclinical submission - Efficacy and safety data (in the intended species) and protocol to support the conduct of clinical studies relative to a single dosage form, route of administration and indication in one species | 17,505 | 19,780 |
| Preclinical submission - Efficacy data and protocol to support the conduct of clinical studies relative to a single route of administration and indication with a dosage form for which a notice of compliance has been issued for use in the species to be treated | 13,997 | 15,816 |
| Preclinical submission - For food-producing animals, toxicity, metabolism and residue depletion studies to establish a temporary acceptable daily intake, a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in one species | 52,506 | 59,332 |
| Preclinical submission - For food-producing animals, toxicity, metabolism and residue depletion studies to establish an acceptable daily intake with a safety factor of 1,000, a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in one species | 78,793 | 89,035 |
| Preclinical submission - For food-producing animals, toxicity, metabolism and residue depletion studies to establish an acceptable daily intake with a safety factor of less than 1,000, a maximum residue limit and a withdrawal period for a single dosage form, dosage and route of administration in one species | 105,044 | 118,700 |
| Preclinical submission - For food-producing animals (once an acceptable daily intake with a safety factor of 1,000 or less has been established), metabolism studies to establish a withdrawal period for a single dosage form, dosage and route of administration in an additional species | 26,254 | 29,667 |
| Preclinical submission - Chemistry and manufacturing data to support a single dosage form containing a non-compendial medicinal ingredient | 17,505 | 19,780 |
| Preclinical submission - Chemistry and manufacturing data to support a single dosage form containing a compendial medicinal ingredient | 8,756 | 9,893 |
| Sale of new drug for emergency treatment - Information to support the sale of a new drug to be used in the emergency treatment of a non-food-producing animal | 62 | 64 |
| Sale of new drug for emergency treatment - Information to support the sale of a new drug to be used in the emergency treatment of a food-producing animal | 124 | 127 |
| Experimental studies certificate - Information and material to support the issuance of an experimental studies certificate for a drug to be administered to a non-food-producing animal | 1,161 | 1,181 |
| Experimental studies certificate - Information and material to support the issuance of an experimental studies certificate whose protocol is the same as that of a previously authorized experimental studies certificate for a drug to be administered to a non-food-producing animal | 582 | 592 |
| Experimental studies certificate - Information and material to support the issuance of an experimental studies certificate for a drug to be administered to a food-producing animal | 3,498 | 3,558 |
| Experimental studies certificate - Information and material to support the issuance of an experimental studies certificate whose protocol is the same as that of a previously authorized experimental studies certificate for a drug to be administered to a food-producing animal | 582 | 592 |
| Notifiable change - Information and material to support an application for a notifiable change | 4,705 | 5,316 |
| Protocol - A protocol that is filed with the Minister and may support a new drug submission, an abbreviated new drug submission, a supplement to a new drug submission or abbreviated new drug submission, a preclinical submission or information and material that is filed for the purpose of obtaining an experimental studies certificate | 4,705 | 5,316 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Human drugs - Disinfectant (item 1) | 1,730 | 1,760 |
| Human drugs - Non-prescription (item 2) | 3,334 | 3,391 |
| Human drugs - Prescription (drug other than one referred to in item 1 or 2) | 5,531 | 5,626 |
| Veterinary drugs | 567 | 577 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Human use - Fabrication - Sterile dosage form | 49,558 | 50,401 |
| Human use - Importation | 38,265 | 38,916 |
| Human use - Fabrication - Non-sterile dosage form | 36,740 | 37,365 |
| Human use - Distribution | 19,531 | 19,864 |
| Human use - Wholesaling | 11,398 | 11,592 |
| Human use - Packaging/labelling | 7,164 | 7,286 |
| Human use - Testing | 5,913 | 6,014 |
| Human use - Building outside Canada (each) | 1,088 | 1,107 |
| Veterinary use - Fabrication - Sterile dosage form | 49,215 | 50,401 |
| Veterinary use - Importation | 38,265 | 38,916 |
| Veterinary use - Fabrication - Non-sterile dosage form | 31,671 | 37,365 |
| Veterinary use - Distribution | 17,437 | 19,864 |
| Veterinary use - Wholesaling | 6,973 | 8,864 |
| Veterinary use - Packaging/labelling | 7,164 | 7,286 |
| Veterinary use - Testing | 4,744 | 6,014 |
| Veterinary use - Building outside Canada (each) | 1,088 | 1,107 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Dealer's Licence Fees - Human Drugs | 5,958 | 6,078 |
| Dealer's Licence Fees - Veterinary Drugs | 2,155.66 | 2,192.31 |
| Dealer's Licence Fees - Veterinary Drugs (first year) | 1,077.84 | 1,096.16 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Certificate of Supplementary Protection | 10,564 | 10,776 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Certificate of Pharmaceutical Product | 102 | 105 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| New Master Files (file registration) | 1,407 | 1,436 |
| Drug Master Files (DMF) - Letter of Access | 200 | 204 |
| Drug Master Files (DMF) - Update | 611 | 624 |
Biocides
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Biocide full review - novel biocide | 41,685 | 42,394 |
| Biocide full review - tier I | 8,595 | 8,742 |
| Biocide full review - tier II | 11,469 | 11,664 |
| Biocide full review - tier III | 13,523 | 13,753 |
| Biocide comparison - labelling only | 2,748 | 2,795 |
| Biocide comparison - administrative application | 975 | 992 |
| Biocide - use of foreign decisions | 3,100 | 3,153 |
| Biocide monograph | 1,861 | 1,893 |
| Biocide major change — monograph | 1,363 | 1,387 |
| Biocide major change — quality and risks | 4,955 | 5,040 |
| Biocide minor change | 1,363 | 1,387 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Fees for Right to Sell Biocides | 1,535 | 1,562 |
Medical devices
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Applications for Class II licence | 632 | 643 |
| Applications for Class II licence amendment | 325 | 331 |
| Applications for Class III licence | 13,926 | 14,163 |
| Applications for Class III licence (near patient) | 29,664 | 30,169 |
| Applications for Class III licence amendment - Changes in manufacturing | 4,395 | 4,470 |
| Applications for Class III licence amendment - Significant changes not related to manufacturing | 11,178 | 11,369 |
| Applications for Class IV licence | 30,199 | 30,713 |
| Applications for Class IV licence amendment - Changes in manufacturing | 4,395 | 4,470 |
| Applications for Class IV licence amendment - Significant changes not related to manufacturing | 15,979 | 16,251 |
| Applications for Class II, III or IV licence or licence amendment - Private label medical device | 176 | 179 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Medical device right to sell | 452 | 460 |
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Application for new licence and annual review of licence | 5,426 | 5,519 |
Pesticides
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Product Chemistry - active ingredient | 5,714 | 5,829 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Product Chemistry - end-use product or manufacturing concentrate | 3,183 | 3,247 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Toxicology data accompanying an application to register a pest control product that contains a new active ingredient | 88,824 | 90,601 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Toxicology data accompanying an application to register a pest control product - or to amend a pest control product - that contains a registered active ingredient | 18,550 | 18,921 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Toxicology data - acute toxicity studies | 3,465 | 3,535 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Exposure data accompanying an application to register a pest control that consists of or that contains a new active ingredient | 20,506 | 20,917 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Exposure data accompanying an application to register a pest control product - or to amend the registration of a pest control product - that contains a registered active ingredient, when a new risk assessment is necessary | 6,751 | 6,887 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Exposure data - other | 6,113 | 6,236 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Metabolism data | 33,915 | 34,594 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Residue data | 18,560 | 18,932 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environment fate data accompanying an application to register a pest control product that consists of or that contains a new active ingredient | 50,016 | 51,017 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environmental fate data accompanying an application to register a pest control product, or to amend the registration of a pest control product, that contains a registered active ingredient, when a new risk assessment is necessary | 27,698 | 28,252 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environmental fate data - other | 13,532 | 13,803 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environment toxicology data accompanying an application to register a pest control product that consists of or that contains a new active ingredient | 43,681 | 44,555 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environmental toxicology data accompanying an application to register a pest control product, or to amend the registration of a pest control product, that contains a registered active ingredient, when a new risk assessment is necessary | 27,760 | 28,316 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Environmental toxicology data - other | 2,893 | 2,951 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Value and effectiveness data for a pest control product | 1,066 | 1,088 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Identification of compensable data | 2,537 | 2,588 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Registration of a new active ingredient - Food use | 8,482 | 8,652 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Registration of a new active ingredient - Non-food use | 5,090 | 5,192 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - New risk assessment necessary - environmental fate data, environmental toxicity data or exposure data | 3,395 | 3,463 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - Data required, label changes | 1,699 | 1,733 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - Data required, other | 1,362 | 1,390 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - No data required | 344 | 351 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Registration of new active ingredient | 683 | 697 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration | 344 | 351 |
| Fees for other applications in respect of a Pest Control Product - Research authorization - Major crops, other than research authorizations set out in paragraphs (c) and (d) | 5,955 | 6,075 |
| Fees for other applications in respect of a Pest Control Product - Research authorization - Minor use crops, other than research authorizations set out in paragraphs (c) and (d) | 5,955 | 6,075 |
| Fees for other applications in respect of a Pest Control Product - Research authorization - Microbial agents, semiochemicals and any substance listed in subparagraph 1(d) (ii) of these regulations | 1,430 | 1,459 |
| Fees for other applications in respect of a Pest Control Product - Research authorization - Greenhouse crops and non-agricultural uses | 1,430 | 1,459 |
| Fees for other applications in respect of a Pest Control Product - Research notifications | 294 | 300 |
| Fees for other applications in respect of a Pest Control Product - Registration of active ingredient to be used in pest control product manufactured only for export | 9,174 | 9,358 |
| Fees for other applications in respect of a Pest Control Product - Amendment to Registration of active ingredient to be used in pest control product manufactured only for export | 1,333 | 1,360 |
| Fees for other applications in respect of a Pest Control Product - Specification of maximum residue limit for a previously unexamined pest control product | 147,002 | 149,943 |
| Fees for other applications in respect of a Pest Control Product - Specification of maximum residue limit for an unregistered use of a previously examined pest control product | 18,560 | 18,932 |
| Applications not Mentioned in Schedules - Processing | 1,333 | 1,360 |
| Applications not Mentioned in Schedules - Fees for applications that do not require an evaluation, as outlined under Section 4 of the Pest Control Products Fees and Charges Regulations (Notification applications only) | 294 | 300 |
| Applications not Mentioned in Schedules - Renewal | 96 | 98 |
| Annual Charge | The lesser of $4,434.51 and 4% of the actual gross revenue during the registrant's preceding fiscal year, but not less than $123.17 | The lesser of $4,509.90 and 4% of the actual gross revenue during the registrant's preceding fiscal year, but not less than $125.26 |
Hazardous materials
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Original Claim (up to 15) | 2,217.26 | 2,254.95 |
| Original Claim (between 16-25) | 492.73 | 501.11 |
| Original Claim (26+) | 246.36 | 250.55 |
| Refiled Claim (up to 15) | 1,773.81 | 1,803.96 |
| Refiled Claim (between 16-25) | 394.18 | 400.88 |
| Refiled Claim (26+) | 197.09 | 200.44 |
Cannabis
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Licence Application Screening Fee - Licence for micro-cultivation | 2,023 | 2,058 |
| Licence Application Screening Fee - Licence for standard cultivation | 4,040 | 4,109 |
| Licence Application Screening Fee - Licence for a nursery | 2,023 | 2,058 |
| Licence Application Screening Fee - Licence for micro-processing | 2,023 | 2,058 |
| Licence Application Screening Fee - Licence for standard processing | 4,040 | 4,109 |
| Licence Application Screening Fee - Licence for sale for medical purposes | 4,040 | 4,109 |
| Application for a security clearance | 2,041 | 2,076 |
| Application for import or export permit | 754 | 767 |
| Annual fee - Licence for micro-cultivation | (a) If the cannabis revenue is $1 million or less, the greater of 1% of the cannabis revenue, and $2,500; or (b) if the cannabis revenue is greater than $1 million, the maximum amount determinable under paragraph (a) plus 2.3% of the amount by which the cannabis revenue exceeds $1 million. |
|
| Annual fee - Licence for standard cultivation | The greater of 2.3% of the cannabis revenue and $23,000. | |
| Annual fee - Licence for a nursery | (a) If the cannabis revenue is $1 million or less, the greater of 1% of the cannabis revenue, and $2,500; or (b) if the cannabis revenue is greater than $1 million, the maximum amount determinable under paragraph (a) plus 2.3% of the amount by which the cannabis revenue exceeds $1 million. |
|
| Annual fee - Licence for micro-processing | (a) If the cannabis revenue is $1 million or less, the greater of 1% of the cannabis revenue, and $2,500; or (b) if the cannabis revenue is greater than $1 million, the maximum amount determinable under paragraph (a) plus 2.3% of the amount by which the cannabis revenue exceeds $1 million. |
|
| Annual fee - Licence for standard processing | The greater of 2.3% of the cannabis revenue and $23,000. | |
| Annual fee - Licence for medical purposes | The greater of 2.3% of the cannabis revenue and $23,000. | |
Tobacco
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Annual charge for a designated manufacturer | N/A | A designated manufacturer's annual charge for each fiscal year is to be calculated according to the formula A ÷ B × C where A is the designated manufacturer's total net sales revenue for the previous fiscal year; B is the aggregate of the total net sales revenue of all designated manufacturers for the previous fiscal year; and C is the annual cost base for the previous fiscal year. |
National dosimetry services
| Fee | Fee amount in 2025-2026 (CAD $) |
Fee amount in 2026-2027 (CAD $) |
|---|---|---|
| Annual support | 101.40 | 103.10 |
| Annual support - multi-group discount (5+ groups) | 66.80 | 67.90 |
| Shipping and handling (per shipment) | 14.50 | 14.50 |
| Processing fees: 1-2 Inlight/TLD Dosimeter Quarterly | 12.60 | 12.80 |
| Processing fees: 1-2 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 10.80 | 11 |
| Processing fees: 1-2 Ring Dosimeter Monthly/Quarterly | 12.80 | 13.00 |
| Processing fees: 1-2 Neutron Dosimeter Monthly/Quarterly | 18 | 18.30 |
| Processing fees: 3-4 Inlight/TLD Dosimeter Quarterly | 11.60 | 11.80 |
| Processing fees: 3-4 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 8.70 | 8.80 |
| Processing fees: 3-4 Ring Dosimeter Monthly/Quarterly | 12.10 | 12.30 |
| Processing fees: 3-4 Neutron Dosimeter Monthly/Quarterly | 16.90 | 17.20 |
| Processing fees: 5-6 Inlight/TLD Dosimeter Quarterly | 10.50 | 10.70 |
| Processing fees: 5-6 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 8 | 8.10 |
| Processing fees: 5-6 Ring Dosimeter Monthly/Quarterly | 11 | 11.20 |
| Processing fees: 5-6 Neutron Dosimeter Monthly/Quarterly | 15.90 | 16.20 |
| Processing fees: 7-8 Inlight/TLD Dosimeter Quarterly | 9.50 | 9.70 |
| Processing fees: 7-8 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.70 | 7.80 |
| Processing fees: 7-8 Ring Dosimeter Monthly/Quarterly | 10 | 10.20 |
| Processing fees: 7-8 Neutron Dosimeter Monthly/Quarterly | 14.90 | 15.20 |
| Processing fees: 9-14 Inlight/TLD Dosimeter Quarterly | 8.50 | 8.60 |
| Processing fees: 9-14 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.40 | 7.50 |
| Processing fees: 9-14 Ring Dosimeter Monthly/Quarterly | 9 | 9.20 |
| Processing fees: 9-14 Neutron Dosimeter Monthly/Quarterly | 13.90 | 14.10 |
| Processing fees: 15-22 Inlight/TLD Dosimeter Quarterly | 8 | 8.10 |
| Processing fees: 15-22 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.20 | 7.30 |
| Processing fees: 15-22 Ring Dosimeter Monthly/Quarterly | 8.70 | 8.80 |
| Processing fees: 15-22 Neutron Dosimeter Monthly/Quarterly | 12.80 | 13 |
| Processing fees: 23-34 Inlight/TLD Dosimeter Quarterly | 7.40 | 7.50 |
| Processing fees: 23-34 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6.90 | 7 |
| Processing fees: 23-34 Ring Dosimeter Monthly/Quarterly | 8.20 | 8.30 |
| Processing fees: 23-34 Neutron Dosimeter Monthly/Quarterly | 11.60 | 11.80 |
| Processing fees: 35-49 Inlight/TLD Dosimeter Quarterly | 7.20 | 7.30 |
| Processing fees: 35-49 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6.70 | 6.80 |
| Processing fees: 35-49 Ring Dosimeter Monthly/Quarterly | 7.70 | 7.80 |
| Processing fees: 35-49 Neutron Dosimeter Monthly/Quarterly | 11 | 11.20 |
| Processing fees: 50+ Inlight/TLD Dosimeter Quarterly | 6.20 | 6.30 |
| Processing fees: 50+ Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6.20 | 6.30 |
| Processing fees: 50+ Ring Dosimeter Monthly/Quarterly | 6.70 | 6.80 |
| Processing fees: 50+ Neutron Dosimeter Monthly/Quarterly | 10.50 | 10.70 |
| Ad hoc dosimeter request — add-on (per shipment) | 75 | 75 |
| Priority processing request (per request) | 110 | 110 |
| Pregnancy service (semi-monthly) | 375 | 375 |
| Electronic personal dosimeter rental (per 9 months) | 322.50 | 322.50 |
| Electronic personal dosimeter rental with beta module (per 9 months) | 375 | 375 |
| Specialized consultation (per hour) | 125 | 125 |
| Customized reporting (per hour) | 70 | 70 |
| NDR dose modifications (per hour) | 75 | 75 |
| Reprinting reports (per report) | 25 | 25 |
| Overdue dosimeter (three months after wearing period ends) | 48.50 | 48.50 |
| Late dosimeter (six months after wearing period ends) | 48.50 | 48.50 |
| Lost/damaged dosimeter | 80 | 80 |
| Damaged electronic personal dosimeter | 430 | 430 |
| Credit upon returning overdue dosimeter | 24 | 24 |
| Credit upon returning late or lost dosimeter | 40 | 40 |