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Home » Topics » Regulatory » Health Canada

Health Canada
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Regulatory front for Feb. 11, 2021

Feb. 11, 2021
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: MITA announces new health care supplier standard; Laggardly patient record response costs provider $75k; New med-tech resource platform now includes logistics; Spectrascience the subject of speculation, SEC action; HC nudging along with regulatory modernization plan.
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Woman stands in front of COVID-19 screening system

Health Canada approves Monitio’s COVID-19 screening system

Jan. 29, 2021
By David Godkin
TORONTO – Startup CEOs may sometimes be forgiven a little exuberance on learning their technology has received the high sign from regulatory officials. So it was when the head of Monitio Intelligence Inc. Ben Su sifted through his email at his office in Coburg Ontario and saw the Health Canada logo at the top of the letter. “I was actually jumping up and down when I received that authorization letter. I was very excited,” Su said. Since then Su has been overseeing installation of an automated COVID-19 screening system.
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Regulatory front for Jan. 27, 2021

Jan. 27, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Health Canada updates list of recognized standards; FTC posts draft consent agreement for Flo Health; Two more snared in PGx testing scam.
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Regulatory front

Klobuchar worried about data security for Amazon Halo

Dec. 14, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: USTR seeking input on nations with poor IP protections; NICE sticks with ABI to evaluate PAD; Health Canada to extend COVID-19 flexibilities.
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Health Canada approves Lynparza as treatment of BRCA or ATM gene-mutated mCRPC

Nov. 26, 2020
Regulatory front

TGA hits pause on two consultations

Nov. 18, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: HQO recommends home UVB therapy; Health Canada announces testing advisory panel.
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Regulatory front

Health Canada posts notice for UV decontamination

Nov. 12, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA eyes grant of license for spectrometer for SARS; HQO eyes TAVI/TAVR for low-risk patients; ACLA says testing capacity beginning to strain.
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Product image

Songbird flying high with Health Canada approval of double biomarker COVID-19 test device

Oct. 2, 2020
By David Godkin
TORONTO – Health Canada has approved a portable COVID-19 test kit which began as a testing regime for identifying pathogens, microbes and viruses in the European food and natural products industry. The Hyris Bcube developed by Guelph, Ontario-based Songbird Life Science Inc., in partnership with London, U.K.’s Hyris Ltd., is described as a portable DNA-based “laboratory in a box” for coronavirus testing in large urban spaces as well as more remote, indigenous communities in Canada’s north.
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Allergan withdraws uterine fibroid drug Fibristal from Canadian market

Oct. 1, 2020
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The Virtual Medtech Conference

Maisel: FDA developing plans for EUA devices for post-pandemic review

Sep. 30, 2020
By Mark McCarty
The COVID-19 pandemic has not run its course, but the U.S. FDA is already working on a plan for handling devices in the period after the public health emergency ends. Bill Maisel, chief medical officer at the FDA’s Center for Device and Radiological Health (CDRH), said the agency is thinking through what would have to appear in a guidance for a transition that may span a number of months, providing industry with some much-needed breathing room.
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