Canada Gazette, Part I, Volume 154, Number 48: GOVERNMENT NOTICES
November 28, 2020
DEPARTMENT OF THE ENVIRONMENT
CANADIAN ENVIRONMENTAL PROTECTION ACT, 1999
Significant New Activity Notice No. 20405
Significant New Activity Notice
(Section 85 of the Canadian Environmental Protection Act, 1999)
Whereas the Minister of the Environment and the Minister of Health have assessed information in their possession in respect of the substance graphene, Chemical Abstracts Service Registry Number 1034343-98-0, under section 83 of the Canadian Environmental Protection Act, 1999;
Whereas the substance is not specified on the Domestic Substances List;
And whereas the ministers suspect that a significant new activity in relation to the substance may result in the substance becoming toxic within the meaning of section 64 of the Act,
Therefore, the Minister of the Environment indicates, pursuant to section 85 of the Canadian Environmental Protection Act, 1999, that subsection 81(4) of that act applies with respect to the substance in accordance with the Annex.
The Honourable Jonathan Wilkinson
Minister of the Environment
ANNEX
Information Requirements
(Section 85 of the Canadian Environmental Protection Act, 1999)
1. The following definition applies in this notice:
- “substance”
- means the substance graphene, Chemical Abstracts Service Registry Number 1034343-98-0.
2. (1) If the substance meets the characteristics mentioned in subsection 3(1), a significant new activity is
- (a) the use of the substance in the manufacture of any of the following products in which the substance is present in a concentration that is greater than or equal to 1% by weight:
- (i) a consumer product to which the Canada Consumer Product Safety Act applies, which is applied as a spray, mist or aerosol, or
- (ii) a cosmetic, as defined in section 2 of the Food and Drugs Act, which is applied as a spray, mist or aerosol;
- (b) the distribution for sale of the substance in a quantity greater than 10 kg in a calendar year in any of the following products in which the substance is present in a concentration that is greater than or equal to 1% by weight:
- (i) a consumer product to which the Canada Consumer Product Safety Act applies, which is applied as a spray, mist or aerosol, or
- (ii) a cosmetic, as defined in section 2 of the Food and Drugs Act, which is applied as a spray, mist or aerosol.
(2) If the substance meets the characteristics mentioned in subsection 3(2), a significant new activity is any use involving the substance in a quantity that
- (a) exceeds 100 kg, but is equal to or less than 1 000 kg in a calendar year;
- (b) exceeds 1 000 kg, but is equal to or less than 10 000 kg in a calendar year; or
- (c) exceeds 10 000 kg in a calendar year.
3. (1) For the purposes of subsection 2(1), the substance must have the following characteristics:
- (a) a primary particle lateral size distribution within the range of 0.3 to 10 micrometres;
- (b) a number of atomic layers within the range of 2 to 15 layers;
- (c) a carbon to oxygen ratio that is greater than or equal to 89;
- (d) a purity greater than or equal to 84%; and
- (e) a surface modification with sodium dodecyl sulphate.
(2) For the purposes of subsection 2(2), the substance must have at least one of the following characteristics:
- (a) a primary particle lateral size distribution outside the range of 0.3 to 10 micrometres;
- (b) a number of atomic layers outside the range of 2 to 15 layers;
- (c) a carbon to oxygen ratio that is less than 89;
- (d) a purity that is less than 84%; or
- (e) a surface modification other than with sodium dodecyl sulphate.
4. Despite section 2, a use of the substance is not a significant new activity if the substance is used
- (a) as a research and development substance or as a site-limited intermediate substance as those terms are defined in subsection 1(1) of the New Substances Notification Regulations (Chemicals and Polymers); or
- (b) in a consumer product or a cosmetic, as described in that section, that is for export only.
5. For each proposed significant new activity, the following information must be provided to the Minister of the Environment at least 90 days before the day on which the activity begins:
- (a) a description of the significant new activity in relation to the substance;
- (b) the anticipated annual quantity of the substance to be used in relation to the significant new activity;
- (c) the analytical information that is necessary to determine the primary and secondary particle size distribution of the substance (i.e. length, width and thickness and number of atomic layers);
- (d) the information that is necessary to determine the agglomeration and aggregation state, shape, surface area, surface charge of the substance, and degree of oxidation (i.e. carbon to oxygen ratio);
- (e) all other information or test data in respect of the substance that is in the possession of the person who is proposing the significant new activity, or to which they have access, and that is relevant to identifying the hazards of the substance to the environment and human health and the degree of environmental and public exposure to the substance;
- (f) the name of every government department or agency, either outside or within Canada, to which the person proposing the significant new activity has provided information regarding the use of the substance and, if known, the department’s or agency’s file number and, if any, the outcome of the department’s or agency’s assessment and the risk management actions in relation to the substance imposed by the department or agency;
- (g) the name, civic and postal addresses, telephone number and, if any, the fax number and email address of the person who is proposing the significant new activity and, if they are not a resident in Canada, of the person resident in Canada who is authorized to act on their behalf;
- (h) a certification that the information is accurate and complete, dated and signed by the person who is proposing the significant new activity if they are a resident in Canada or, if not, by the person resident in Canada who is authorized to act on their behalf;
- (i) for any significant new activity described in subsection 2(1)
- (i) a description of the products and, if known, of the end-use products that are anticipated to contain the substance, the intended use of those products and the function of the substance in those products,
- (ii) the information specified in paragraphs 7(c) and (d) of Schedule 4 to the New Substances Notification Regulations (Chemicals and Polymers), and
- (iii) the data and a report from a test in respect of the substance that is conducted in accordance with the methodology described in the Organisation for Economic Co-operation and Development (OECD) Guidelines for the Testing of Chemicals, Test No. 413, entitled Subchronic Inhalation Toxicity: 90-day Study, that is current at the time the test is conducted;
- (j) for any significant new activity referred to in paragraph 2(2)(a)
- (i) the information specified in sections 1 to 7 of Schedule 4 of the New Substances Notification Regulations (Chemicals and Polymers);
- (k) for any significant new activity referred to in paragraph 2(2)(b)
- (i) the information mentioned in paragraph 4(j) or, if that information has been previously provided, the date (year, month, day) of the submission of that information and, if they are known, the new substances pre-notification consultation number, if it has been assigned, and the significant new activity notification number,
- (ii) the information specified in sections 2 to 5, 8, and 10 of Schedule 5 of the New Substances Notification Regulations (Chemicals and Polymers),
- (iii) the data and a report from a test in respect of the substance that is conducted in accordance with the methodology described in the OECD Guidelines for the Testing of Chemicals, Test No. 403, entitled Acute Inhalation Toxicity, that is current at the time the test is conducted,
- (iv) the data and a report from an in vitro mammalian cell mutagenicity test, in respect of the substance that is conducted in accordance with the methodology described in the OECD Guidelines for the Testing of Chemicals, Test No. 476, entitled In Vitro Mammalian Cell Gene Mutation Test; or the OECD Test No. 490, entitled In Vitro Mammalian Cell Gene Mutation Tests using the Thymidine Kinase Gene, that is current at the time the test is conducted;
- (l) for any significant new activity referred to in paragraph 2(2)(c)
- (i) the information mentioned in paragraph 4(k) or, if that information has been previously provided, the date (year, month, day) of the submission of that information and, if they are known, the new substances pre-notification consultation number, if it has been assigned, and the significant new activity notification number,
- (ii) the information specified in sections 2, 3, 5, 6, 9, 10, and 11 of Schedule 6 to the New Substances Notification Regulations (Chemicals and Polymers), and
- (iii) the data and a report from a test in respect of the substance, that is conducted in accordance with the methodology described in the OECD Guidelines for the Testing of Chemicals, Test No. 413, entitled Subchronic Inhalation Toxicity: 90-day Study, that is current at the time the test is conducted.
6. (1) The test data and the test report described in subparagraphs 5(i)(iii), (k)(iii), (iv) and (l)(iii) must be developed in accordance with the practices described in the OECD Principles of Good Laboratory Practice set out in Annex II of the Decision of the Council Concerning the Mutual Acceptance of Data in the Assessment of Chemicals, adopted on May 12, 1981, that are current at the time the test data are developed.
(2) Furthermore, all tests regarding the substance must be conducted in accordance with the principles described in the Guidance on Sample Preparation and Dosimetry for the Safety Testing of Manufactured Nanomaterials (OECD Series on the Safety of Manufactured Nanomaterials, No. 36) that is current at the time the test data are developed.
7. The information referred to in paragraphs 5(c) and (d) must be obtained in accordance with the principles described in the Report of the OECD Expert Meeting on the Physical Chemical Properties of Manufactured Nanomaterials and Test Guidelines (OECD Series on the Safety of Manufactured Nanomaterials, report No. 41), that are current at the time the test data are developed.
8. The information in item 5 will be assessed within 90 days after the day on which it is received by the Minister of the Environment.
Transitional provisions
9. Despite subsection 2(1), in the period between the date of publication of the present notice and November 27, 2021, if the substance meets the characteristics mentioned in subsection 3(1), a significant new activity is
- (a) the use of the substance in a quantity greater than or equal to 100 kg in a calendar year in the manufacture of any of the following products in which the substance is present in a concentration that is greater than or equal to 1% by weight:
- (i) a consumer product to which the Canada Consumer Product Safety Act applies, that is applied as a spray, mist or aerosol, or
- (ii) a cosmetic, as defined in section 2 of the Food and Drugs Act, that is applied as a spray, mist or aerosol; and
- (b) the distribution for sale of the substance in a quantity greater than or equal to 100 kg in a calendar year, in any of the following products, in which the substance is present in a concentration that is greater than or equal to 1% by weight:
- (i) a consumer product to which the Canada Consumer Product Safety Act applies, that is applied as a spray, mist or aerosol, or
- (ii) a cosmetic, as defined in section 2 of the Food and Drugs Act, which is applied as a spray, mist or aerosol.
10. For greater certainty, in respect of the calendar year 2021, the quantity of substance that is used before November 28 of that calendar year is not considered for the purposes of subsection 2(1).
EXPLANATORY NOTE
(This explanatory note is not part of the Significant New Activity Notice.)
Description
This Significant New Activity (SNAc) Notice is a legal instrument adopted by the Minister of the Environment pursuant to section 85 of the Canadian Environmental Protection Act, 1999 (the Act) to apply the SNAc provisions of that Act to the substance graphene, Chemical Abstracts Service Registry Number 1034343-98-0. The Notice is now in force and it is a binding law. It is therefore mandatory for a person who intends to use the substance for a significant new activity as defined in the Notice to meet all the applicable requirements set out the Notice.
A SNAc Notice does not constitute an endorsement from the Minister of the Environment, the Department of the Environment or the Government of Canada of the substance to which it relates, nor does it constitute an exemption from any other laws or regulations that are in force in Canada and that may apply to this substance or activities involving the substance.
Applicability of the Significant New Activity Notice
The Notice requires that any person (individual or corporation) engaging in a significant new activity in relation to the substance graphene, Chemical Abstracts Service Registry Number 1034343-98-0, submit a Significant New Activity notification (SNAN) containing all of the information prescribed in the Notice at least 90 days prior to using the substance for the significant new activity.
In order to address the human toxicity concerns, the Notice requires notification in relation to the use of the substance, with the characteristics mentioned in the Notice, in the manufacture of consumer products or cosmetics that are applied as a spray, mist or aerosol, when the substance is present in a concentration greater than or equal to 1% by weight. The Notice also requires notification in relation to the distribution for sale of consumer products or cosmetics that are applied as a spray, mist or aerosol when the substance, with the characteristics mentioned in the Notice, is present in a concentration greater than or equal to 1% by weight and when the total quantity of the substance involved is more than 10 kg in a calendar year. For example, notification is required if a person plans to manufacture an aerosol hair sprays where the concentration of the substance, with the characteristics mentioned in the Notice, in the hair spray is 1.5% by weight.
In order to address environmental and human toxicity concerns, notification is required for any use of the substance in Canada involving more than 100 kg of the substance in a calendar year and when the substance has at least one of the characteristics mentioned in the notice. For example, notification is required if a person plans to use 101 kg in a calendar year of the substance with 16 atomic layers.
A SNAN is required 90 days before the use of the substance in a significant new activity.
Activities not subject to the Notice
Uses of the substance that are regulated under the Acts of Parliament listed in Schedule 2 of the Act, including the Pest Control Products Act, the Fertilizers Act and the Feeds Act are excluded from the Notice. The Notice also does not apply to transient reaction intermediates, impurities, contaminants, partially unreacted materials, or in some circumstances to items such as, but not limited to, wastes, mixtures, or manufactured items. However, it should be noted that individual components of a mixture may be subject to notification under the provisions of the Act. See subsection 81(6) and section 3 of the Act, and section 3 of the Guidelines for the Notification and Testing of New Substances: Chemicals and Polymers for additional information.
Activities involving the use of the substance as a research and development substance or a site-limited intermediate or an export-only product are excluded from the Notice. The terms “research and development substance” and “site-limited intermediate substance” are defined in subsection 1(1) of the New Substances Notification Regulations (Chemicals and Polymers).
Information to be submitted
The Notice sets out the information that must be provided to the Minister 90 days before the day on which the substance graphene, Chemical Abstracts Service Registry Number 1034343-98-0, is used for a significant new activity. The Department of the Environment and the Department of Health will use the information submitted in the SNAN to conduct risk assessments within 90 days after the complete information is received.
The assessment of the substance identified concerns associated with potential activities involving use of the substance in consumer products or cosmetics that are applied as a spray, mist or aerosol, and with activities involving the substance at the nanoscale. The Significant New Activity Notice is issued to gather information to ensure that the substance will undergo further assessment before significant new activities are undertaken.
The information requirements in the Notice relate to general information in respect of the substance, details surrounding its use, exposure information, and toxicity to human health and the environment. Some of the information requirements reference the New Substances Notification Regulations (Chemicals and Polymers).
Additional guidance on preparing a SNAN can be found in section 1.3 of the Guidelines for the Notification and Testing of New Substances: Chemicals and Polymers.
Transitional provision
A transitional provision is included in the Notice to facilitate compliance by persons who may already have imported or manufactured up to 100 kg of the substance and started activities with it in concentrations that are greater than or equal 1% by weight in a consumer product or cosmetic. The Notice comes into force immediately.
However, if the substance is used in the manufacture or the distribution for sale of a consumer product as defined in the Canada Consumer Product Safety Act or a cosmetic as defined in the Food and Drugs Act, in a concentration that is greater than or equal to 1% by weight, a quantity of less than 100 kg may be used for the period between the publication of the Notice and November 27, 2021. On November 28, 2021, the threshold will be lowered.
The transitional provisions do not apply to activities involving the substance specified in subsection 2(2) of the Notice.
Compliance
When assessing whether or not a substance is subject to SNAc provisions, a person is expected to make use of information in their possession or to which they may reasonably have access. This means information in any of the notifier’s offices worldwide or other locations where the notifier can reasonably have access to the information. For example, manufacturers are expected to have access to their formulations, while importers or users of a substance, mixture, or product are expected to have access to import records, usage information and the relevant Safety Data Sheets (SDSs), formerly “Material Safety Data Sheets” (MSDSs). More details are contained in the Regulations Amending the New Substances Notification Regulations (Chemicals and Polymers) and the Export of Substances on the Export Control List Regulations for reference to this amendment.
Although an SDS is an important source of information on the composition of a product, it should be noted that the goal of the SDS is to protect the health of workers in the workplace from specific hazards of chemical products. Therefore, an SDS may not list all product ingredients that may be subject to a SNAc notice due to human health or the environmental concerns. Any person requiring more detailed information on product composition is encouraged to contact their supplier.
If any information becomes available that reasonably supports the conclusion that the substance is toxic or capable of becoming toxic, the person who is in possession of or that has knowledge of the information and is involved in activities with the substance is obligated, under section 70 of the Act, to provide that information to the Minister without delay.
A company can submit a SNAN on behalf of its clients. For example, in cases where a person takes possession or control of a substance from another person, they may not be required to submit a SNAN, under certain conditions, if their activities were covered by an original SNAN submitted by the person from whom they obtained the substance. The Substances Management Advisory Note “(ARCHIVED) Clarification in relation to the submission of Significant New Activity Notifications in application of the Canadian Environmental Protection Act, 1999” provides more detail on this subject.
Under section 86 of the Act, any person who transfers the physical possession or control of a substance subject to a SNAc notice must notify all persons to whom the physical possession or control is transferred of the obligation to comply with the notice, including the obligation to notify the Minister of any SNAc and to provide all the required information outlined above.
A pre-notification consultation (PNC) is recommended for notifiers who wish to consult with the program during the planning or preparation of their SNAN to discuss any questions or concerns they have about the prescribed information and test plans.
For further information, please contact the Substances Management Information Line (eccc.substances.eccc@canada.ca (email), 1‑800‑567‑1999 [toll-free in Canada], and 819‑938‑3232 [outside of Canada]).
The Act is enforced in accordance with the publicly available Compliance and Enforcement Policy for the Canadian Environmental Protection Act. In instances of non-compliance, consideration is given to factors such as the nature of the alleged violation, potential harm, intent, and history of compliance.
DEPARTMENT OF THE ENVIRONMENT
CANADIAN ENVIRONMENTAL PROTECTION ACT, 1999
Waiver of information requirements for living organisms (subsection 106(9) of the Canadian Environmental Protection Act, 1999)
Whereas, any person who proposes to import or manufacture a living organism that is not on the Domestic Substances List must provide to the Minister of the Environment the information required under subsection 106(1) of the Canadian Environmental Protection Act, 1999; and
Whereas, a person may, pursuant to subsection 106(8) of the Canadian Environmental Protection Act, 1999, request any of the requirements to provide information under subsection 106(1) of the Canadian Environmental Protection Act, 1999 to be waived.
Therefore, notice is hereby given, pursuant to subsection 106(9) of the Canadian Environmental Protection Act, 1999, that the Minister of the Environment waived some requirements to provide information in accordance with the following annex pursuant to subsection 106(8) of that Act.
Thomas Kruidenier
Acting Executive Director
Program Development and Engagement Division
On behalf of the Minister of the Environment
ANNEX
Person to whom a waiver was granted | Information concerning a living organism in relation to which a waiver was granted |
---|---|
Adaptimmune LLC | Data from tests to determine the effects of the living organism on aquatic plant, invertebrate, and vertebrate species likely to be exposed |
Data from tests to determine the effects of the living organism on terrestrial plant, invertebrate, and vertebrate species likely to be exposed | |
Data from tests of antibiotic susceptibility | |
BioVectra Inc. | Data from tests of antibiotic susceptibility |
Celgene Inc. | Data from tests to determine the effects of the living organism on aquatic plant, invertebrate, and vertebrate species likely to be exposed (2) table b1 note 1 |
Data from tests to determine the effects of the living organism on terrestrial plant, invertebrate, and vertebrate species likely to be exposed (2) | |
Data from tests of antibiotic susceptibility (2) | |
Merck Canada Inc. | Data from tests to determine the effects of the living organism on aquatic plant, invertebrate, and vertebrate species likely to be exposed |
Data from tests to determine the effects of the living organism on terrestrial plant, invertebrate, and vertebrate species likely to be exposed | |
Data from tests of antibiotic susceptibility | |
Oncorus, Inc. | Data from tests to determine the effects of the living organism on aquatic plant, invertebrate, and vertebrate species likely to be exposed |
Data from tests to determine the effects of the living organism on terrestrial plant, invertebrate, and vertebrate species likely to be exposed | |
Pfizer Canada Inc. | Data from tests to determine the effects of the living organism on aquatic plant, invertebrate, and vertebrate species likely to be exposed |
Data from tests to determine the effects of the living organism on terrestrial plant, invertebrate, and vertebrate species likely to be exposed | |
Data from tests of antibiotic susceptibility | |
Table b1 note(s)
|
EXPLANATORY NOTE
The decision to grant a waiver is made on a case-by-case basis by the Minister of the Environment in consultation with the Minister of Health. Every year an average of 500 regulatory declarations are submitted for chemicals, polymers and living organisms under subsections 81(1), (3) and (4) and 106(1), (3) and (4) of the Canadian Environmental Protection Act, 1999 and around 100 waivers are granted yearly for chemicals, polymers and living organisms under subsections 81(8) and 106(8) of the Canadian Environmental Protection Act, 1999.
For more information, please see the waivers web page on the New Substances website.
DEPARTMENT OF THE ENVIRONMENT
CANADIAN ENVIRONMENTRAL POTECTION ACT, 1999
Waiver of information requirements for substances (subsection 81(9) of the Canadian Environmental Protection Act, 1999)
Whereas any person who proposes to import or manufacture a substance that is not on the Domestic Substances List must provide to the Minister of the Environment the information required under subsection 81(1) of the Canadian Environmental Protection Act, 1999; and
Whereas a person may, pursuant to subsection 81(8) of the Canadian Environmental Protection Act, 1999, request any of the requirements to provide information under subsection 81(1) of the Canadian Environmental Protection Act, 1999 to be waived.
Therefore, notice is hereby given, pursuant to subsection 81(9) of the Canadian Environmental Protection Act, 1999, that the Minister of the Environment waived some requirements to provide information pursuant to subsection 81(8) of that Act and in accordance with the following annex.
Thomas Kruidenier
Acting Executive Director
Program Development and Engagement Division
On behalf of the Minister of the Environment
ANNEX
Person to whom a waiver was granted | Information concerning a substance in relation to which a waiver was granted |
---|---|
AstraZeneca Canada Inc. | Data in respect of vapour pressure |
Data in respect of octanol/water partition coefficient | |
Data from a ready biodegradation test | |
Data from an acute toxicity test for the most sensitive species: fish, daphnia or algae | |
BASF Canada Inc. | Data in respect of hydrolysis as a function of pH |
Eastman Chemical Co. | Data in respect of density |
Lubrizol Canada Limited | Data in respect of hydrolysis as a function of pH |
Data from an in vivo mammalian mutagenicity test for chromosomal aberrations or gene mutations | |
NanoXplore Inc. | Data in respect of boiling point |
Data in respect of vapour pressure | |
Data in respect of octanol/water partition coefficient | |
Nouryon Functional Chemicals LLC | Data in respect of boiling point |
Data from an in vivo mammalian mutagenicity test for chromosomal aberrations or gene mutations | |
Novozymes North America | Data in respect of melting point |
Data in respect of boiling point | |
Data in respect of density | |
Data in respect of vapour pressure | |
Data in respect of water solubility | |
Data in respect of octanol/water partition coefficient |
EXPLANATORY NOTE
The decision to grant a waiver is made on a case-by-case basis by the Minister of the Environment in consultation with the Minister of Health. Every year an average of 500 regulatory declarations are submitted for chemicals, polymers and living organisms under subsections 81(1), (3) and (4) and 106(1), (3) and (4) of the Canadian Environmental Protection Act, 1999 and around 100 waivers are granted yearly for chemicals, polymers and living organisms under subsections 81(8) and 106(8) of the Canadian Environmental Protection Act, 1999.
For more information, please see the waivers web page on the New Substances website.
DEPARTMENT OF HEALTH
CANADIAN ENVIRONMENTAL PROTECTION ACT, 1999
Proposed Guidelines for Canadian Drinking Water Quality for Bromoxynil
Pursuant to subsection 55(3) of the Canadian Environmental Protection Act, 1999, the Minister of Health hereby gives notice of proposed Guidelines for Canadian Drinking Water Quality for Bromoxynil. The proposed guideline document is available for comment from November 28, 2020, to January 27, 2021, on the Health Canada consultation webpage. Any person may, within 60 days after publication of this notice, file with the Minister of Health written comments on the proposed document. Comments must be sent by email at HC.water-eau.SC@canada.ca, or by regular mail to the Water and Air Quality Bureau, Health Canada, 269 Laurier Avenue West, A.L. 4903D, Ottawa, Ontario K1A 0K9.
November 28, 2020
David Morin
Director General
Safe Environments Directorate
On behalf of the Minister of Health
ANNEX
Proposed guideline
A maximum acceptable concentration (MAC) of 0.03 mg/L (30 µg/L) is proposed for bromoxynil in drinking water.
Executive summary
This guideline technical document was prepared in collaboration with the Federal-Provincial-Territorial Committee on Drinking Water and is based on assessments of bromoxynil completed by Health Canada’s Pest Management Regulatory Agency and supporting documents.
Exposure
Bromoxynil is a registered herbicide used to control broadleaf weeds in food and feed crops. In 2017 (the most recent year for which data are available), more than 1 million kilograms of bromoxynil were sold in Canada. Bromoxynil may be released into the environment as surface run-off, through spray drift or while adsorbed to dust particles.
Canadian data indicate that bromoxynil is not commonly found in source or drinking water but may be found at low levels in source and drinking water in agricultural areas where it is applied. Bromoxynil is rarely detected in foods.
Health effects
Animal studies indicate that bromoxynil primarily targets the liver. At higher doses, bromoxynil has been found to cause developmental effects (skeletal effects, decreased pup weight) but no reproductive effects. There are no human studies on the effects of bromoxynil on the liver. The proposed MAC of 0.03 mg/L (30 µg/L) is based on an increase in clinical signs (i.e. effects founded on actual observation as distinguished from theoretical or experimental effects; panting, salivation, liquid feces, pale gums) and liver weight, as well as decreases in body weight and body weight gain observed in a one-year dog study.
Analytical and treatment considerations
The establishment of drinking water guidelines takes into consideration the ability to both measure the contaminant and remove it from drinking water supplies. Several analytical methods are available for measuring bromoxynil in water at concentrations well below the proposed MAC.
At the municipal level, there is limited information on the efficiency of treatment technologies to remove bromoxynil from drinking water. Oxidation, advanced oxidation processes, and biofiltration achieved a wide range of removals. Activated carbon adsorption and membrane processes are expected to be effective. Although bromoxynil may be removed using oxidation, utilities should be aware of the potential formation of degradation by-products. Pilot- and/or bench-scale testing are recommended prior to full-scale implementation.
For bromoxynil removal at a small system or household level, for example when the drinking water supply is from a private well, a residential drinking water treatment unit may be an option. Although there are no treatment units currently certified for the removal of bromoxynil from drinking water, technologies that are expected to be effective include adsorption (activated carbon) and reverse osmosis. When using such a treatment unit, it is important to send samples of water entering and leaving the treatment unit to an accredited laboratory for analysis to ensure that adequate bromoxynil removal is occurring.
Application of the guideline
Note: Specific guidance related to the implementation of drinking water guidelines should be obtained from the appropriate drinking water authority in the affected jurisdiction.
The proposed guideline for bromoxynil is protective against health effects from exposure to bromoxynil in drinking water over a lifetime. Any exceedance of the proposed MAC should be investigated and followed by the appropriate corrective actions if required. For exceedances in source water where there is no treatment in place, additional monitoring to confirm the exceedance should be conducted. If it is confirmed that source water bromoxynil concentrations are above the proposed MAC, then an investigation to determine the most appropriate way to reduce exposure to bromoxynil should be conducted. This may include use of an alternate water supply or installation of treatment. Where treatment is already in place and an exceedance occurs, an investigation should be conducted to verify treatment and determine if adjustments are needed to lower the treated water concentration below the proposed MAC.
International considerations
Other national and international organizations have drinking water guidelines, standards and/or guidance values for bromoxynil in drinking water. Variations in these values can be attributed to the age of the assessments or to differing policies and approaches, including the choice of key study and the use of different consumption rates, body weights and source allocation factors.
Australia’s National Health and Medical Research Council has established a guideline value of 0.01 mg/L (10 μg/L) for bromoxynil in drinking water based on decreased body weights in a one-year dog study. The United States Environmental Protection Agency has not set a regulatory value for bromoxynil in drinking water. Similarly, the World Health Organization does not have a guideline for bromoxynil.
The European Union (EU) does not have a specific parametric value for individual pesticides. Instead, the EU has a value of 0.1 μg/L for any individual (single) pesticide, and a value of 0.5 μg/L for total pesticides found in drinking water. In establishing these values, the EU did not consider the science related to each pesticide, such as health effects. Instead, the values are based on a policy decision to keep pesticides out of drinking water.
DEPARTMENT OF HEALTH
HAZARDOUS MATERIALS INFORMATION REVIEW ACT
Filing of claims for exemption
A supplier can file a claim for exemption under the Hazardous Materials Information Review Act (HMIRA) with Health Canada from having to disclose information under the Hazardous Products Act (HPA) and Hazardous Products Regulations (HPR) that they consider to be confidential business information (CBI) on a safety data sheet (SDS) or label associated with a hazardous product.
An employer can also file a claim for exemption under the HMIRA with Health Canada from having to disclose information under the Canada Labour Code or the provisions of the Accord Act that they consider to be CBI on an SDS or label associated with a hazardous product.
Notice is hereby given of the filing of claims for exemption under the HMIRA listed in the table below.
Lynn Berndt-Weis
Director
Workplace Hazardous Materials Bureau
Consumer and Hazardous Products Safety Directorate
Healthy Environments and Consumer Safety Branch
Claimant | Product Identifier | Subject of the Claim for Exemption | Registry Number |
---|---|---|---|
Momentive Performance Materials | Silquest* A-2387 | C.i. and C. of one ingredient | 03388823 |
Afton Chemical Company | HiTEC® 4142M Fuel Additive | C.i. of one ingredient | 03389456 |
3M Canada Company | 3M™ Polyurethane Sealant 540 (Various Colours) | C. of two ingredients | 03389565 |
Secure Energy Services | SECURE MO-8910 | C.i. and C. of
one ingredient C. of one ingredient |
03389735 |
King Industries, Inc. | NA-SUL® CA-1122 | C.i. and C. of
one ingredient C. of one ingredient |
03389740 |
ChampionX Canada ULC | ACPC12261B | C.i. and C. of two ingredients | 03390400 |
King Industries, Inc. | K-KAT® XK-682 | C.i. and C. of one ingredient | 03390557 |
Pacer Chemical Inc. | Prosolve 120 | C.i. and C. of three ingredients | 03390558 |
Pacer Chemical Inc. | Prosolve 110 | C.i. and C. of two ingredients | 03390559 |
Advancing Chemistry Inc. | W-SPA-HT | C.i. and C. of eight ingredients | 03390717 |
Produits Environnementaux Greensolv inc. | WHEELSTRIP PREMIUM | C.i. and C. of four ingredients | 03390868 |
Afton Chemical Corporation | HiTEC® 013 Performance Additive | C.i. of two ingredients | 03390948 |
Advancing Chemistry Inc. | W-SPA | C.i. and C. of five ingredients | 03390949 |
The Lubrizol Corporation | LUBRIZOL® 9688 | C.i. of four ingredients | 03391104 |
Chemtrade Logistics Inc. | Pass C Plus (+) | C.i. of one ingredient | 03391398 |
Allnex Canada Inc., c/o Goodmans, LLP | EBECRYL® 3214 radiation curing resins | C.i. of one ingredient | 03391605 |
Momentive Performance Materials | Niax* silicone L-6164 | C.i. and C. of one ingredient | 03391606 |
Shell Catalysts& Technologies | CENTERA GT Catalyst DN-3655 | C.i. of two ingredients | 03391607 |
W-Tech Technologies Ltd. | Vanfloc MRC 4500 | C.i. of one ingredient | 03391761 |
W-Tech Technologies Ltd. | Vanmist 210 | C.i. of two ingredients | 03391762 |
3M Canada Company | 3M™ Scotch-Weld™ Low Odour Acrylic Adhesive 8805NS Green, Part B | C. of one ingredient | 03391763 |
3M Canada Company | 3M™ Scotch-Weld™ Epoxy Adhesive 110 Gray, Part A | C. of one ingredient | 03391764 |
Note: C.i. = chemical identity and C. = concentration
DEPARTMENT OF INDUSTRY
OFFICE OF THE REGISTRAR GENERAL
Appointments
- Canada Industrial Relations Board
- Full-time member
- Cameron, Elizabeth, Order in Council 2020-866
- Canadian High Arctic Research Station
- Chairperson of the Board of Directors
- Kunuk, Joe Adla, Order in Council 2020-878
- Members of the Board of Directors
- Barnes, Karen, Order in Council 2020-880
- Fairman, Kimberly, Order in Council 2020-879
- Pepper-Journal, Jacqueline, Order in Council 2020-881
- President
- Hubbard, Jennifer C., Order in Council 2020-882
- Parole Board of Canada
- Part-time member
- Payette, Normand H., Order in Council 2020-853
November 19, 2020
Diane Bélanger
Official Documents Registrar
OFFICE OF THE SUPERINTENDENT OF FINANCIAL INSTITUTIONS
BANK ACT
Royal Bank of Canada — Exemption
Notice is hereby given, pursuant to subsection 156.05(4) of the Bank Act (the “Act”), that the management of Royal Bank of Canada (“RBC”) has, pursuant to subsection 156.05(3) of the Act, been exempted from the requirement of paragraph 156.05(1)(a) of the Act to send the prescribed management proxy circular to each shareholder whose proxy is solicited for the annual meeting of shareholders to be held on or about April 8, 2021, and any subsequent annual and/or special meetings.
The exemption is granted on the basis that RBC makes the prescribed management proxy circular accessible, as well as sends a notice thereof, in accordance with National Instrument 51-102 Continuous Disclosure Obligations and National Instrument 54-101 Communication with Beneficial Owners of Securities of a Reporting Issuer, to each shareholder whose proxy is solicited.
This exemption was granted on November 6, 2020.
November 28, 2020
Jeremy Rudin
Superintendent of Financial Institutions
PRIVY COUNCIL OFFICE
Appointment opportunitie
We know that our country is stronger — and our government more effective — when decision-makers reflect Canada’s diversity. The Government of Canada has implemented an appointment process that is transparent and merit-based, strives for gender parity, and ensures that Indigenous peoples and minority groups are properly represented in positions of leadership. We continue to search for Canadians who reflect the values that we all embrace: inclusion, honesty, fiscal prudence, and generosity of spirit. Together, we will build a government as diverse as Canada.
We are equally committed to providing a healthy workplace that supports one’s dignity, self-esteem and the ability to work to one’s full potential. With this in mind, all appointees will be expected to take steps to promote and maintain a healthy, respectful and harassment-free work environment.
The Government of Canada is currently seeking applications from diverse and talented Canadians from across the country who are interested in the following positions.
Current opportunities
The following opportunities for appointments to Governor in Council positions are currently open for applications. Every opportunity is open for a minimum of two weeks from the date of posting on the Governor in Council appointments website.
Position | Organization | Closing date |
---|---|---|
Member | Atlantic Pilotage Authority Canada | |
President and Chief Executive Officer | Atomic Energy of Canada Limited | |
Member | Buffalo and Fort Erie Public Bridge Authority | |
Director | Business Development Bank of Canada | |
Director — Board Risk Committee Chairperson | Business Development Bank of Canada | |
President and Chief Executive Officer | Canada Development Investment Corporation | |
Commissioner for Employers | Canada Employment Insurance Commission | |
President and Chief Executive Officer | Canada Lands Company Limited | |
President | Canada Mortgage and Housing Corporation | |
Member of the Board of Directors | Canada Post | |
Member (Federal) |
Canada–Newfoundland and Labrador Offshore Petroleum Board | |
President | Canadian Commercial Corporation | |
Member | Canadian Cultural Property Export Review Board | |
Commissioner (full-time), Commissioner (part-time) |
Canadian Energy Regulator | |
Director | Canadian Energy Regulator | |
Chief Commissioner | Canadian Grain Commission | |
Commissioner | Canadian Grain Commission | |
Member | Canadian Human Rights Tribunal | |
Chairperson | Canadian International Trade Tribunal | |
Chairperson | Canadian Museum of History | |
Director | Canadian Museum of History | |
Permanent Member | Canadian Nuclear Safety Commission | |
Chairperson | Canadian Transportation Agency | |
Temporary Member | Canadian Transportation Agency | |
Chief Administrator | Courts Administration Service | |
Director | Farm Credit Canada | |
Chairperson | Federal Public Sector Labour Relations and Employment Board | |
Vice-Chairperson | Federal Public Sector Labour Relations and Employment Board | |
Director | Freshwater Fish Marketing Corporation | |
Chairperson | Great Lakes Pilotage Authority Canada | |
Director (Federal) |
Hamilton-Oshawa Port Authority | |
Member, Northwest Territories | Historic Sites and Monuments Board of Canada | |
Assistant Deputy Chairperson | Immigration and Refugee Board of Canada | |
Commissioner | Impact Assessment Agency of Canada | |
Member (appointment to roster) |
International Trade and International Investment Dispute Settlement Bodies | |
Chairperson | The Jacques Cartier and Champlain Bridges Incorporated | |
Chairperson | Laurentian Pilotage Authority Canada | |
Chairperson | Military Police Complaints Commission of Canada | |
Member | Military Police Complaints Commission of Canada | |
Director (Federal) |
Nanaimo Port Authority | |
Member | National Arts Centre Corporation | |
Secretary | National Battlefields Commission | |
Member | National Seniors Council | |
Member | Natural Sciences and Engineering Research Council of Canada | |
Veterans’ Ombudsman | Office of the Veterans Ombudsman | |
Member | Payments in Lieu of Taxes Dispute Advisory Panel | |
Director | Public Sector Pension Investment Board | |
Commissioner | Roosevelt Campobello International Park Commission | |
Member | Social Sciences and Humanities Research Council of Canada | |
President | Social Sciences and Humanities Research Council of Canada | |
Registrar | Supreme Court of Canada | |
Member | Telefilm Canada | |
Chairperson and Member | Transportation Appeal Tribunal of Canada | |
Member | Transportation Appeal Tribunal of Canada | |
Vice-Chairperson | Transportation Appeal Tribunal of Canada |
TREASURY BOARD SECRETARIAT
MEMBERS OF PARLIAMENT RETIRING ALLOWANCES ACT
2021, 2022 and 2023 member contribution rates for the Members of Parliament pension plan
In accordance with subsection 2.7(10) of the Members of Parliament Retiring Allowances Act, the contribution rates, footnote 1 for calendar years 2021, 2022 and 2023, fixed under subsection 2.7(1) of the Act, are as follows:
1. Contribution rates prior to reaching the 75% maximum pension accrual
Calendar Year |
Under Age 71 | Ages 71 and Above | Combined | |||
---|---|---|---|---|---|---|
Below YMPE table b5 note a | YMPE to MPE table b5 note b | Above MPE | Combined | |||
2021 | 13.42 | 17.13 | 0.00 | 13.40 | 0.00 | 12.47 |
2022 | 13.62 | 17.39 | 0.00 | 13.59 | 0.00 | 12.47 |
2023 | 13.67 | 17.45 | 0.00 | 13.66 | 0.00 | 12.47 |
Table b5 note(s)
|
Calendar Year |
Under Age 71 | Ages 71 and Above | Combined | ||
---|---|---|---|---|---|
Below MPE table b6 note a | Above MPE | Combined | |||
2021 | 7.55 | 23.34 | 9.94 | 23.34 | 10.87 |
2022 | 7.31 | 23.34 | 9.75 | 23.34 | 10.87 |
2023 | 7.26 | 23.34 | 9.68 | 23.34 | 10.87 |
Table b6 note(s)
|
Calendar Year |
Under Age 71 | Ages 71 and Above | Combined | |||
---|---|---|---|---|---|---|
Below YMPE table b7 note a | YMPE to MPE table b7 note b | Above MPE | Combined | |||
2021 | 20.97 | 24.69 | 23.34 | 23.34 | 23.34 | 23.34 |
2022 | 20.94 | 24.70 | 23.34 | 23.34 | 23.34 | 23.34 |
2023 | 20.93 | 24.71 | 23.34 | 23.34 | 23.34 | 23.34 |
Table b7 note(s)
|
2. Contribution rates upon reaching the 75% maximum pension accrual
Calendar Years 2021 to 2023 | MPRA Account | MPRCA Account |
---|---|---|
Members under age 71 | 1.00% (salary up to MPE table b8 note a ) | 1.00% (salary above the MPE table b8 note a ) |
Members 71 and above | 0.00% | 1.00% |
Table b8 note(s)
|
Jean-Yves Duclos
President of the Treasury Board
BANK OF CANADA
ASSETS |
Amount |
Total |
---|---|---|
Cash and foreign deposits |
6.7 |
|
Loans and receivables |
||
Securities purchased under resale agreements |
155,096.3 |
|
Advances to members of Payments Canada |
1.0 |
|
Other receivables |
4.7 |
|
155,102.0 |
||
Investments |
||
Government of Canada treasury bills |
69,682.9 |
|
Government of Canada bonds – carried at amortized cost |
101,546.8 |
|
Government of Canada bonds – carried at fair value through profit and loss |
169,267.1 |
|
Canada Mortgage Bonds |
9,645.2 |
|
Other bonds |
11,113.1 |
|
Securities lent or sold under repurchase agreements |
1,793.8 |
|
Other securities |
5,355.3 |
|
Shares in the Bank for International Settlements (BIS) |
505.4 |
|
368,909.6 |
||
Derivatives — Indemnity agreements with the Government of Canada | 277.2 |
|
Capital assets |
||
Property and equipment |
570.4 |
|
Intangible assets |
74.1 |
|
Right-of-use leased assets |
46.1 |
|
|
690.6 |
|
Other assets |
34.7 |
|
Total assets |
525,020.8 |
LIABILITIES AND EQUITY |
Amount |
Total |
---|---|---|
Bank notes in circulation |
103,601.3 |
|
Deposits |
||
Government of Canada |
106,176.2 |
|
Members of Payments Canada |
303,453.9 |
|
Other deposits |
9,010.4 |
|
418,640.5 |
||
Securities sold under repurchase agreements |
1,087.0 |
|
Derivatives — Indemnity agreements with the Government of Canada |
— |
|
Other liabilities |
1,094.6 |
|
524,423.4 |
||
Equity |
||
Share capital |
5.0 |
|
Statutory and special reserves |
125.0 |
|
Investment revaluation reserve |
467.4 |
|
597.4 |
||
Total Liabilities and Equity |
525,020.8 |
I declare that the foregoing statement is correct according to the books of the Bank.
Ottawa, November 18, 2020
Coralia Bulhoes
Chief Financial Officer and Chief Accountant
I declare that the foregoing statement is to the best of my knowledge and belief correct, and shows truly and clearly the financial position of the Bank, as required by section 29 of the Bank of Canada Act.
Ottawa, November 18, 2020
Tiff Macklem
Governor