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
- National dosimetry services
Drugs (human and veterinary)
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| New active substance | 590,346 | 606,286 |
| Clinical or non-clinical data and chemistry and manufacturing data | 305,690 | 313,944 |
| Clinical or non-clinical data only | 122,232 | 125,533 |
| Comparative studies | 68,889 | 70,750 |
| Chemistry and manufacturing data only | 42,384 | 43,529 |
| Clinical or non-clinical data only, in support of safety upgrades to the labelling | 22,372 | 22,977 |
| Labelling only | 6,161 | 6,328 |
| Labelling only (generic drugs) | 2,315 | 2,378 |
| Administrative submission | 975 | 1,002 |
| Disinfectant - Full review | 12,839 | 13,186 |
| Labelling only (disinfectants) | 2,886 | 2,964 |
| Drug identification number application - Labelling standards | 1,861 | 1,912 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (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 | 2,257 | 2,606 |
| Application for drug identification number - Published references or other data | 1,569 | 1,812 |
| 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 | 786 | 906 |
| 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 | 562 | 578 |
| 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.) | 50,015 | 57,787 |
| 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 | 30,298 | 35,006 |
| 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 | 72,735 | 84,038 |
| New Drug Submission - Efficacy and safety data (in the intended species) to support a growth promotion or production enhancement indication in one animal species | 98,491 | 113,795 |
| New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support an additional route of administration | 9,079 | 10,491 |
| New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support each additional strength | 1,505 | 1,739 |
| 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 | 68,199 | 78,793 |
| 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 | 90,918 | 105,044 |
| 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 | 9,079 | 10,491 |
| 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 | 45,446 | 52,506 |
| New Drug Submission - Chemistry and manufacturing data for a non-compendial medicinal ingredient of a drug | 15,150 | 17,505 |
| New Drug Submission - Chemistry and manufacturing data to support one strength of a single dosage form | 15,150 | 17,505 |
| 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 | 7,578 | 8,756 |
| New Drug Submission - Documentation to support a change of manufacturer | 786 | 906 |
| Supplement to a New Drug Submission - Efficacy data to support an additional indication in one animal species | 39,406 | 45,528 |
| 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 | 30,298 | 35,006 |
| Supplement to a New Drug Submission - Efficacy and safety data (in the intended species) to support an indication in another animal species | 50,015 | 57,787 |
| 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 | 72,735 | 84,038 |
| 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 | 98,491 | 113,795 |
| 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 | 24,225 | 27,990 |
| Supplement to a New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support an additional route of administration | 9,079 | 10,491 |
| Supplement to a New Drug Submission - Comparative (pharmacodynamics, clinical or bioavailability) data to support each additional strength | 1,505 | 1,739 |
| 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 | 9,079 | 10,491 |
| 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 | 45,446 | 52,506 |
| 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 | 22,724 | 26,254 |
| 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 | 18,187 | 21,013 |
| 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 | 15,150 | 17,505 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in formulation or dosage form | 7,578 | 8,756 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in packaging or in the sterilization process | 6,043 | 6,982 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support an extension of the expiry dating | 4,541 | 5,246 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support the concurrent use of two drugs | 4,541 | 5,246 |
| Supplement to a New Drug Submission - Chemistry and manufacturing data to support a change in the manufacturing site for parenteral dosage forms | 1,505 | 1,739 |
| Supplement to a New Drug Submission - Documentation to support a change to the name of a manufacturer or the brand name of a drug | 786 | 906 |
| 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 | 9,079 | 10,491 |
| 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 | 9,079 | 10,491 |
| 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 | 15,150 | 17,505 |
| Abbreviated New Drug Submission and Supplement to an Abbreviated New Drug Submission - Chemistry and manufacturing data to support a single dosage form | 15,150 | 17,505 |
| 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. | 786 | 906 |
| 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 | 15,150 | 17,505 |
| 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 | 12,114 | 13,997 |
| 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 | 45,446 | 52,506 |
| 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 | 68,199 | 78,793 |
| 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 | 90,918 | 105,044 |
| 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 | 22,724 | 26,254 |
| Preclinical submission - Chemistry and manufacturing data to support a single dosage form containing a non-compendial medicinal ingredient | 15,150 | 17,505 |
| Preclinical submission - Chemistry and manufacturing data to support a single dosage form containing a compendial medicinal ingredient | 7,578 | 8,756 |
| 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 | 60 | 62 |
| 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 | 120 | 124 |
| 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 | 1,130 | 1,161 |
| 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 | 566 | 582 |
| 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 | 3,406 | 3,498 |
| 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 | 566 | 582 |
| Notifiable change - Information and material to support an application for a notifiable change | 4,072 | 4,705 |
| 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 | 4,072 | 4,705 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Human drugs - Disinfectant (item 1) | 1,684 | 1,730 |
| Human drugs - Non-prescription (item 2) | 3,246 | 3,334 |
| Human drugs - Prescription (drug other than one referred to in item 1 or 2) | 5,385 | 5,531 |
| Veterinary drugs | 552 | 567 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Human use - Fabrication - Sterile dosage form | 48,255 | 49,558 |
| Human use - Importation | 37,259 | 38,265 |
| Human use - Fabrication - Non-sterile dosage form | 35,774 | 36,740 |
| Human use - Distribution | 19,017 | 19,531 |
| Human use - Wholesaling | 11,098 | 11,398 |
| Human use - Packaging/labelling | 6,975 | 7,164 |
| Human use - Testing | 5,757 | 5,913 |
| Human use - Building outside Canada (each) | 1,059 | 1,088 |
| Veterinary use - Fabrication - Sterile dosage form | 47,588 | 49,215 |
| Veterinary use - Importation | 30,099 | 38,265 |
| Veterinary use - Fabrication - Non-sterile dosage form | 24,671 | 31,671 |
| Veterinary use - Distribution | 13,583 | 17,437 |
| Veterinary use - Wholesaling | 5,431 | 6,973 |
| Veterinary use - Packaging/labelling | 6,975 | 7,164 |
| Veterinary use - Testing | 3,695 | 4,744 |
| Veterinary use - Building outside Canada (each) | 1,059 | 1,088 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Dealer’s Licence Fees - Human Drugs | 5,841 | 5,958 |
| Dealer’s Licence Fees - Veterinary Drugs | 2,098.99 | 2,155.66 |
| Dealer’s Licence Fees - Veterinary Drugs (first year) | 1,049.50 | 1,077.84 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Certificate of Supplementary Protection | 10,356 | 10,564 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Certificate of Pharmaceutical Product | 100 | 102 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| New Master Files (file registration) | 1,379 | 1,407 |
| Drug Master Files (DMF) - Letter of Access | 196 | 200 |
| Drug Master Files (DMF) - Update | 599 | 611 |
Biocides
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Biocide full review – novel biocide | N/A | 41,685 |
| Biocide full review — tier I | N/A | 8,595 |
| Biocide full review — tier II | N/A | 11,469 |
| Biocide full review — tier III | N/A | 13,523 |
| Biocide comparison — labelling only | N/A | 2,748 |
| Biocide comparison — administrative application | N/A | 975 |
| Biocide — use of foreign decisions | N/A | 3,100 |
| Biocide monograph | N/A | 1,861 |
| Biocide major change — monograph | N/A | 1,363 |
| Biocide major change — quality and risks | N/A | 4,955 |
| Biocide minor change | N/A | 1,363 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Fees for Right to Sell Biocides | N/A | 1,535 |
Medical devices
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Applications for Class II licence | 615 | 632 |
| Applications for Class II licence amendment | 316 | 325 |
| Applications for Class III licence | 13,559 | 13,926 |
| Applications for Class III licence (near patient) | 28,884 | 29,664 |
| Applications for Class III licence amendment - Changes in manufacturing | 4,279 | 4,395 |
| Applications for Class III licence amendment - Significant changes not related to manufacturing | 10,884 | 11,178 |
| Applications for Class IV licence | 29,405 | 30,199 |
| Applications for Class IV licence amendment - Changes in manufacturing | 4,279 | 4,395 |
| Applications for Class IV licence amendment - Significant changes not related to manufacturing | 15,558 | 15,979 |
| Applications for Class II, III or IV licence or licence amendment - Private label medical device | 171 | 176 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Medical Device Right to Sell | 440 | 452 |
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Application for new licence and annual review of licence | 5,283 | 5,426 |
Pesticides
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (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 | 5,601 | 5,714 |
| 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 | 3,120 | 3,183 |
| 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 | 87,082 | 88,824 |
| 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 | 18,186 | 18,550 |
| 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 | 3,397 | 3,465 |
| 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 | 20,103 | 20,506 |
| 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 | 6,618 | 6,751 |
| 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 | 5,993 | 6,113 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Metabolism data | 33,250 | 33,915 |
| Fees for application to register, or to amend the registration of, a Pest Control Product other than a semiochemical or Microbial Agent - Residue data | 18,196 | 18,560 |
| 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 | 49,035 | 50,016 |
| 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 | 27,154 | 27,698 |
| 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 | 13,266 | 13,532 |
| 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 | 42,824 | 43,681 |
| 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 | 27,215 | 27,760 |
| 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 | 2,836 | 2,893 |
| 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 | 1,045 | 1,066 |
| 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 | 2,487 | 2,537 |
| 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 | 8,315 | 8,482 |
| 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 | 4,990 | 5,090 |
| 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 | 3,328 | 3,395 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - Data required, label changes | 1,665 | 1,699 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - Data required, other | 1,335 | 1,362 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration - No data required | 337 | 344 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Registration of new active ingredient | 669 | 683 |
| Fees for application in respect of a Pest Control Product that is a semiochemical or Microbial Agent - Amendment of registration | 337 | 344 |
| 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) | 5,838 | 5,955 |
| 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) | 5,838 | 5,955 |
| 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 | 1,401 | 1,430 |
| Fees for other applications in respect of a Pest Control Product - Research authorization - Greenhouse crops and non-agricultural uses | 1,401 | 1,430 |
| Fees for other applications in respect of a Pest Control Product - Research notifications | 288 | 294 |
| 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 | 8,994 | 9,174 |
| 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 | 1,306 | 1,333 |
| Fees for other applications in respect of a Pest Control Product - Specification of maximum residue limit for a previously unexamined pest control product | 144,119 | 147,002 |
| 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 | 18,196 | 18,560 |
| Applications not Mentioned in Schedules - Processing | 1,306 | 1,333 |
| Applications not Mentioned in Schedules - Fees for applications that do not require an evaluation, as outlined under Section 4 of the Pest Control Products Fee and Charge Regulations (Notification applications only) | 288 | 294 |
| Applications not Mentioned in Schedules - Renewal | 94 | 96 |
| Annual Charge | The lesser of $4,317.93 and 4% of the actual gross revenue during the registrant's preceding fiscal year, but not less than $119.93 | 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 |
Hazardous materials
| Fee | Fee amount in 20234-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Original Claim (up to 15) | 2,158.97 | 2,217.26 |
| Original Claim (between 16-25) | 479.78 | 492.73 |
| Original Claim (26+) | 239.88 | 246.36 |
| Refiled Claim (up to 15) | 1,727.18 | 1,773.81 |
| Refiled Claim (between 16-25) | 383.82 | 394.18 |
| Refiled Claim (26+) | 191.91 | 197.09 |
Cannabis
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Licence Application Screening Fee - Licence for micro-cultivation | 1,969 | 2,023 |
| Licence Application Screening Fee - Licence for standard cultivation | 3,933 | 4,040 |
| Licence Application Screening Fee - Licence for a nursery | 1,969 | 2,023 |
| Licence Application Screening Fee - Licence for micro-processing | 1,969 | 2,023 |
| Licence Application Screening Fee - Licence for standard processing | 3,933 | 4,040 |
| Licence Application Screening Fee - Licence for sale for medical purposes | 3,933 | 4,040 |
| Application for a security clearance | 1,987 | 2,041 |
| Application for import or export permit | 734 | 754 |
| 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. | |
National dosimetry services
| Fee | Fee amount in 2024-2025 (CAD $) |
Fee amount in 2025-2026 (CAD $) |
|---|---|---|
| Annual support | 98.75 | 101.40 |
| Annual support - multi-group discount (5+ groups) | 65 | 66.80 |
| Shipping and handling (per shipment) | 14.50 | 14.50 |
| Processing fees: 1-2 Inlight/TLD Dosimeter Quarterly | 12.25 | 12.60 |
| Processing fees: 1-2 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 10.50 | 10.80 |
| Processing fees: 1-2 Ring Dosimeter Monthly/Quarterly | 12.50 | 12.80 |
| Processing fees: 1-2 Neutron Dosimeter Monthly/Quarterly | 17.50 | 18 |
| Processing fees: 3-4 Inlight/TLD Dosimeter Quarterly | 11.25 | 11.60 |
| Processing fees: 3-4 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 8.50 | 8.70 |
| Processing fees: 3-4 Ring Dosimeter Monthly/Quarterly | 11.75 | 12.10 |
| Processing fees: 3-4 Neutron Dosimeter Monthly/Quarterly | 16.50 | 16.90 |
| Processing fees: 5-6 Inlight/TLD Dosimeter Quarterly | 10.25 | 10.50 |
| Processing fees: 5-6 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.75 | 8 |
| Processing fees: 5-6 Ring Dosimeter Monthly/Quarterly | 10.75 | 11 |
| Processing fees: 5-6 Neutron Dosimeter Monthly/Quarterly | 15.50 | 15.90 |
| Processing fees: 7-8 Inlight/TLD Dosimeter Quarterly | 9.25 | 9.50 |
| Processing fees: 7-8 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.50 | 7.70 |
| Processing fees: 7-8 Ring Dosimeter Monthly/Quarterly | 9.75 | 10 |
| Processing fees: 7-8 Neutron Dosimeter Monthly/Quarterly | 14.50 | 14.90 |
| Processing fees: 9-14 Inlight/TLD Dosimeter Quarterly | 8.25 | 8.50 |
| Processing fees: 9-14 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7.25 | 7.40 |
| Processing fees: 9-14 Ring Dosimeter Monthly/Quarterly | 8.75 | 9 |
| Processing fees: 9-14 Neutron Dosimeter Monthly/Quarterly | 13.50 | 13.90 |
| Processing fees: 15-22 Inlight/TLD Dosimeter Quarterly | 7.75 | 8 |
| Processing fees: 15-22 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 7 | 7.20 |
| Processing fees: 15-22 Ring Dosimeter Monthly/Quarterly | 8.50 | 8.70 |
| Processing fees: 15-22 Neutron Dosimeter Monthly/Quarterly | 12.50 | 12.80 |
| Processing fees: 23-34 Inlight/TLD Dosimeter Quarterly | 7.25 | 7.40 |
| Processing fees: 23-34 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6.75 | 6.90 |
| Processing fees: 23-34 Ring Dosimeter Monthly/Quarterly | 8 | 8.20 |
| Processing fees: 23-34 Neutron Dosimeter Monthly/Quarterly | 11.25 | 11.60 |
| Processing fees: 35-49 Inlight/TLD Dosimeter Quarterly | 7 | 7.20 |
| Processing fees: 35-49 Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6.50 | 6.70 |
| Processing fees: 35-49 Ring Dosimeter Monthly/Quarterly | 7.50 | 7.70 |
| Processing fees: 35-49 Neutron Dosimeter Monthly/Quarterly | 10.75 | 11 |
| Processing fees: 50+ Inlight/TLD Dosimeter Quarterly | 6 | 6.20 |
| Processing fees: 50+ Inlight/TLD Dosimeter Semi-Monthly/Monthly | 6 | 6.20 |
| Processing fees: 50+ Ring Dosimeter Monthly/Quarterly | 6.50 | 6.70 |
| Processing fees: 50+ Neutron Dosimeter Monthly/Quarterly | 10.25 | 10.50 |
| 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 |
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