Coronavirus disease (COVID-19): For health professionals

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What health professionals need to know

Health professionals in Canada have a critical role to play in identifying, reporting and managing potential cases of COVID-19.

Coronaviruses are a large family of viruses, some of which infect only animals, and others that can infect humans. Seven strains of coronavirus are now known to cause illness in humans.

The strain of coronavirus found in Wuhan is the most recent of 7 known strains. Of the 6 others, 4 cause only minor respiratory symptoms similar to those of a cold, and 2, severe acute respiratory syndrome (SARS CoV) and Middle East respiratory syndrome (MERS CoV), have been associated with more serious and life-threatening diseases.

Those who are infected with COVID-19 may have little to no symptoms. Symptoms, similar to a cold or flu, may take up to 14 days to appear after exposure to COVID-19. Current studies are investigating if the virus can be transmitted to others if someone is not showing symptoms. Symptoms include:

In severe cases, infection can lead to death.

The World Health Organization (WHO) is actively monitoring the situation and has issued updated information on the outbreak, including a risk assessment, advice on public health measures and infection prevention and control, and enhanced surveillance.

The Public Health Agency of Canada (PHAC) is also monitoring the COVID-19 situation closely and providing updates as new information becomes available.


Current epidemiologic information suggests that human-to-human transmission of COVID-19 can occur when an individual is in close contact with a symptomatic case. Human coronaviruses are most commonly spread from an infected person through: respiratory droplets; close, prolonged personal contact; and touching an infected area, then touching mouth, nose or eyes before washing hands.

Epidemiological information

PHAC is collaborating with provincial and territorial public health partners to collect information on COVID-19 cases in Canada. A detailed epidemiologic summary is available.

Detecting and reporting

Diagnostic testing and medical devices

PHAC's National Microbiology Laboratory (NML) has capacity to identify COVID-19, and is developing and implementing new diagnostic tests, based on the genetic sequence of COVID-19 made available by China on January 10, 2020. Laboratory testing should be initiated in consultation with the respective provincial Public Health Laboratory (PHL). The PHL will then coordinate the submission of specimens to the National Microbiology Laboratory for further testing, as necessary. Refer to Protocol for Microbiological Investigations of Severe Acute Respiratory Infections for details on specimen collection and handling, and regarding consultation with the PHL microbiologist on-call. Refer also to additional laboratory guidance provided by PHLs.

An Interim Order has also been signed to help ensure quicker and more flexible approval of the importation and sale of medical devices that are necessary for Canada's response to COVID-19, including test kits. We have published a list of commercial diagnostic tests authorized for sale in Canada.

An interim order is one of the fastest mechanisms available to the Government of Canada to help make health products available to address larger scale public health emergencies.

If you wish to submit an application for authorization under the Interim Order please contact the Medical Devices Directorate via email or call 613-324-7842.

Health care professionals can obtain COVID-19 diagnostic test kits or supportive devices not yet approved for sale through the Medical Devices Special Access Program.

For general inquiries about the licensing or authorization of medical devices in Canada; you can contact the Medical Devices Directorate at 613-957-7285 or


Health care professionals can refer to the Interim National Surveillance Guidelines for Coronavirus Disease (COVID-19), and the Interim National COVID-19 Case Report Form, to aid with the detection and reporting of COVID-19 in Canada.

Recommendations to public health care professionals

Infection prevention and control

Reprocessing of N-95 Respirators

Healthcare professionals providing direct care to patients across the country above all need access to the personal protective equipment (PPE) they need for each and every shift.

The COVID-19 pandemic has created unprecedented demand for certain supplies, including PPE. The Government of Canada is using a range of strategies to respond to this increased demand by

Reprocessing of devices intended for single use only is not a new concept. It has been done successfully with other devices used in Canada and similar technology can be applied to N95 respirators.

A list of all authorized N95 respirators and all authorized equipment used in the reprocessing of N95 respirators is available on Health Canada's website. A notice to Health Care Professionals is posted on Health Canada's website that provides further information about Health Canada's evidence requirements and basis for the approach.You can also find guidance we have provided to industry on the minimum requirements that must be met to receive an authorization for equipment used in the reprocessing of N95 respirators originally intended for single use only.

Find out more about personal protective equipment for use against COVID-19.


There is currently no vaccine against or specific treatment for COVID-19. Treatment is supportive and should be tailored to the patient's condition.

Refer to the interim guidance on clinical management of patients with moderate to severe COVID-19.

Health Canada publishes a list of all COVID-19 clinical trials in Canada.

Drugs and Vaccines

When a vaccine or drug is developed to prevent or treat COVID-19, we will take appropriate action to ensure availability.

Measures include fast-tracking through the:

Other measures include the:

Special Access to Remdesivir for COVID-19 in Canada

Gilead is transitioning the provision of emergency access to remdesivir from individual compassionate use via Health Canada's Special Access Program requests to access through clinical trials. This approach will both accelerate access to remdesivir for severely ill patients and enable the collection of data from all participating patients. These programs are currently under rapid development in conjunction with national regulatory authorities worldwide including Health Canada. More details on how to participate in clinical trials will be forthcoming.

During this transition period, Gilead is unable to accept new individual Canadian compassionate requests via Health Canada's Special Access Program due to an overwhelming demand.

Gilead is focused now on processing previously approved requests and anticipate the clinical trial will initiate in a similar expected timeframe that any new requests for compassionate use via the Special Access Program would have been processed.

Exceptions will be made only for pregnant women or children less than 18 years of age with confirmed COVID-19 and severe manifestations of disease.


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