Explain the key elements that were introduced in the 2020

Reference no: EM133435518

Question: In 2020, Health Canada introduced a new temporary market authorization pathway for COVID-19 vaccine and drug manufacturers. Explain the outlining the 2020 COVID-19 drug authorization process a Canadian manufacturer of COVID-19 drugs and vaccines could use, as well as the necessary regulatory submission to maintain market authorization in 2021.

Explain the key elements that were introduced in the 2020 authorization pathway to increase authorization efficiency (describe at least 3)

Reference no: EM133435518

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