View source for CPR - WHMIS Manner of Establishing Classification
==WHMIS - Controlled Products Regulations: Manner of Establishing Classification (Section 33)== The legal text of the regulations in section 33 follows below: ==CPR: Section 33, Subsection 1: Manner of Establishing Classification== For the purpose of establishing that a product, material or substance is included in a class listed in Schedule II of the Act or falls into a division of a class, the supplier shall use, subject to subsection (2), *(a) results from testing that he has carried out with respect to the product, material or substance in accordance with sections 34 to 66, as applicable; or *(b) evaluation and scientific judgment based on test results with respect to **(i) the product, material or substance, or **(ii) where appropriate, a product, material or substance that has similar properties. ==CPR: Section 33, Subsection 2: Manner of Establishing Classification== For the purpose of establishing that a product, material or substance is or is not included in Class D — Poisonous and Infectious Material, the supplier may use information of which the supplier is aware or ought reasonably to be aware in place of the criteria set out in subsection (1). ==CPR: Section 33, Subsection 3: Manner of Establishing Classification== Where the test results referred to in paragraph (1)(b) are results from toxicological studies, the studies shall have been carried out in accordance with *(a) the applicable OECD Test Guideline referred to in this Part; or *(b) where there are no tests carried out in accordance with the applicable OECD Test Guidelines referred to in this Part, one of the following tests or methods: **(i) in the case of a 90 day test or a chronic test, a test or method described in U.S. Food and Drug Administration (FDA) guidelines or U.S. Environmental Protection Agency (EPA) guidelines, as published in the Federal Register and as amended from time to time, **(ii) in the case of a test for skin or eye irritation, the Draize Test as described in volume 82 of The Journal of Pharmacology and Experimental Therapeutics, dated 1944, at pages 377 to 390, **(iii) in the case of a test for teratogenicity, a test or method described in Principles for the Testing of Drugs for Teratogenicity, Technical Report Series Number 364, published in 1967 by the World Health Organization, **(iv) in the case of a test for mutagenicity, a test or method described by the U.S. Environmental Protection Agency (EPA) in “Proposed Guidelines for Registering Pesticides in the U.S.; Hazard Evaluation: Human and Domestic Animals”, as published in volume 43 of the Federal Register (No. 163), dated 1978, at pages 37,336 to 37,403, or **(v) any other test or method that is carried out in accordance with generally accepted standards of good scientific practice at the time the test is carried out. SOR/97-543, s. 20(E). ==WHMIS MSDS Reference Manual - Section 33== Health Canada's WHMIS MSDS reference manual for section 33 is available at: [http://www.hc-sc.gc.ca/ewh-semt/pubs/occup-travail/ref_man/cpr-rpc_33_e.html WHMIS Requirements of the HPA and CPR, CPR Section 33]. One of the important points they note is as follows: "A classification system based on cut-off presumes that a mixture is hazardous if it contains a hazardous ingredient at a concentration exceeding a specified cut-off. The use of cut-offs is administratively straightforward and can be applied by using available data on the toxicology of ingredients of the mixture. The cut-off values agreed to for WHMIS are:" "0.1% for teratogens, embryotoxins, carcinogens, reproductive toxins, respiratory tract sensitizers and mutagens; and" "1.0% for all other toxicological effects and tissue corrosivity." "Since WHMIS is an information system, the use of cut-off values appeared justifiable as a means of consistently communicating information about hazardous ingredients as contrasted with providing a hazard evaluation of an untested mixture. The numerical values of the cut-offs, however, are necessarily arbitrary and were chosen largely for consistency between Canada and the United States." ==Nexreg Compliance WHMIS Canadian MSDS Authoring Services== Nexreg Compliance can author a WHMIS compliant Canadian MSDS for your product. For more information on Nexreg's WHMIS MSDS authoring services, please [http://www.nexreg.com/en/nexreg_info/contact_us.php contact Nexreg Compliance] or visit the following links: *[http://www.nexreg.com/en/msds_authoring/whmis_msds_authoring.php Canadian WHMIS MSDS Authoring] (English) *[http://www.nexreg.com/de/msds_authoring/whmis_msds_authoring.php WHMIS Urheberrechtliche Überprüfung MSDS] (German) *[http://www.nexreg.com/es/msds_authoring/whmis_msds_authoring.php Creación de MSDS - Canadá] (Spanish) *[http://www.nexreg.com/fr/msds_authoring/whmis_msds_authoring.php Création WHMIS MSDS] (French) *[http://www.nexreg.com/ko/msds_authoring/whmis_msds_authoring.php 캐나다 MSDS 제작] (Korean) *[http://www.nexreg.com/ja/msds_authoring/whmis_msds_authoring.php カナダ MSDS の作成] (Japanese) *[http://www.nexreg.com/nl/msds_authoring/whmis_msds_authoring.php Schrijven WHMIS MSDS] (Dutch) *[http://www.nexreg.com/zh/msds_authoring/whmis_msds_authoring.php 加拿大物料安全数据表编写服务] (Chinese - Simplified) ==Canadian Goverment Links== *[http://www.hc-sc.gc.ca/ewh-semt/pubs/occup-travail/ref_man/cpr-rpc_33_e.html WHMIS Requirements of the HPA and CPR, CPR Section 33] ==WHMIS MSDS NexregWiki Links== *[[MSDS Authoring in Canada]] == Contact Nexreg Compliance == *'''Toll Free: (866)361-3032''' *E-mail: [mailto:email@example.com firstname.lastname@example.org] *Nexreg USA: (206)418-6663 *Nexreg Canada: (519)488-5126 *Nexreg UK: +44 020 7993 5893 [[Category:Canadian Regulations]] [[Category:MSDS Compliance|MSDS Compliance by Jurisdiction]] [[Category:WHMIS MSDS Compliance|WHMIS MSDS Compliance by Jurisdiction]]
CPR - WHMIS Manner of Establishing Classification
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