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Found 10 records similar to Occupational Health and Safety orders report

Provincial

The Ministry of Labour inspects workplaces to monitor compliance with occupational health and safety legislation and regulations. These are considered to be proactive field visits. The ministry focuses on workplaces and/or sectors of the economy that have a history of poor compliance or high levels of work-related injuries. Data from the Ministry of Labour reflects Occupational Health and Safety (OHS) and Employment Standards (ES) information at a point in time and/or for specific reporting purposes.

Last Updated: Jul. 21, 2022
Date Published: Jan. 11, 2020
Organization: Government of Ontario
Formats: CSV HTML
Keywords:  Justice and Public Safety, Education and Training, Government
Provincial

A claim is a complaint made by a person who believes their employer has violated the Employment Standards Act, 2000. Where an Officer finds a violation of the Act, they assess money owing. This data is regularly updated and is subject to change. Data from the Ministry of Labour reflects Occupational Health and Safety (OHS) and Employment Standards (ES) information at a point in time and/or for specific reporting purposes.

Last Updated: Jul. 21, 2022
Date Published: Jan. 11, 2020
Organization: Government of Ontario
Formats: CSV HTML
Keywords:  Education and Training, Economy and Business, Government
Provincial

This dataset provides total numbers of events that have been reported to the Ministry of Labour. Events are categorized as work refusals, complaints, incidents, illnesses, occurrences, disputes or work stoppages registered with the ministry regarding health and safety issues. Data from the Ministry of Labour reflects Occupational Health and Safety (OHS) and Employment Standards (ES) information at a point in time and/or for specific reporting purposes. As a result, the information above may not align with other data sources From 2011/2012 to 2014/2015, the date range collected is based on the 'event date' data field from the Ministry of Labour Case Management System.

Last Updated: Jul. 21, 2022
Date Published: Jan. 11, 2020
Organization: Government of Ontario
Formats: CSV HTML
Keywords:  Justice and Public Safety, Education and Training, Government
Provincial

The numbers reflect incidents that were reported to and tracked by the Ministry of Labour. They exclude death from natural causes, death of non- workers at a workplace, suicides, death as a result of a criminal act or traffic accident (unless the OHSA is also implicated) and death from occupational exposures that occurred in the past. Data from the Ministry of Labour reflects Occupational Health and Safety (OHS) and Employment Standards (ES) information at a point in time and/or for specific reporting purposes. As a result, the information above may not align with other data sources.

Last Updated: Jul. 21, 2022
Date Published: Jan. 11, 2020
Organization: Government of Ontario
Formats: CSV HTML
Keywords:  Justice and Public Safety, Education and Training, Government
Provincial

A field visit occurs when a ministry inspector visits a workplace to assess compliance with the Occupational Health and Safety Act (OHSA) and regulations. A workplace is considered any land, premises, physical location or thing at, upon, in or near which a worker work. An inspector may visit the same workplace multiple times. During the field visit, the inspector can issue orders to different companies ("contraveners") at a workplace to achieve compliance with OHSA and regulations.

Last Updated: Jul. 21, 2022
Date Published: Jan. 11, 2020
Organization: Government of Ontario
Formats: PDF CSV HTML XLSX
Keywords:  Education and Training, Jobs and employment
Federal

This guidance document provides source establishments with assistance on how to comply with adverse reaction reporting obligations under the Food and Drugs Act and the Safety of Human Cells, Tissues and Organs for Transplantation Regulations

Last Updated: Jun. 1, 2021
Date Published: Nov. 19, 2020
Organization: Health Canada
Formats: HTML
Keywords:  guidance document, source establishments, reporting adverse reactions, safety, human cells, tissues, organs
Federal

Regulated parties must comply with the CCPSA, including the GPs, at all times. Accordingly, regulated parties must always ensure that their consumer products do not pose a danger to human health or safety and must do so proactively, without waiting for communications from Health Canada. This document describes how Health Canada proposes to apply the GP in particular contexts and sets out Health Canada's expectations for regulated parties.

Last Updated: Feb. 14, 2022
Date Published: May 5, 2020
Organization: Health Canada
Formats: HTML
Keywords:  Canada Consumer Product Safety Act, CCPSA, regulated parties, enforcement approach, General Prohibitions, GP
Federal

To provide sponsors of new drug submissions with the information necessary to comply with Sections C.08.002(2)(h), C.08.002.1(2)(c)(ii) and C.08.003(3) of the Food and Drug Regulations (Regulations) with respect to comparative bioavailability studies used in support of the safety and efficacy of a drug.

Last Updated: Jun. 1, 2021
Date Published: Sep. 1, 2018
Organization: Health Canada
Formats: HTML
Keywords:  guidance document, conduct and analysis, comparative bioavailability studies, pharmaceutically equivalent, data requirements and criteria
Federal

To ensure that sponsors of new drug submissions have the information necessary to comply with Sections C.08.002(2)(h), C.08.002.1(2)(c)(ii) and C.08.003(3) of the Food and Drug Regulations with respect to comparative bioavailability and comparative pharmacodynamic studies used in support of the safety and efficacy of a drug.

Last Updated: Jun. 1, 2021
Date Published: Mar. 1, 2018
Organization: Health Canada
Formats: HTML
Keywords:  guidance document, comparative bioavailability standards, comparative pharmacodynamic studies, Food and Drug Regulations, safety of a drug
Federal

This guidance document will help anyone who is involved in the conduct of clinical trials of drugs in humans to understand and comply with Part C, Division 5 of the Food and Drug Regulations (the Regulations).

Last Updated: May 4, 2021
Date Published: Aug. 21, 2019
Organization: Health Canada
Formats: HTML
Keywords:  Guidance, Part C, Division 5, Food and Drug Regulations, Drugs for Clinical Trials, Clinical Trials Involving Human Subjects, GUI-0101
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