During the UK Covid-19 inquiry, Michael Gove faced allegations of attempting to bypass the regulatory process to secure NHS ventilator approvals for James Dyson. Gove, who was the chancellor of the Duchy of Lancaster, responded to claims asserting he pressured the Medicines and Healthcare products Regulatory Agency (MHRA) for swift approval. Evidence revealed the unrealistic urgency surrounding Dyson's product, leading to questions about safety oversight. Gove emphasized his role was not to interfere with the regulatory agency, despite having more involvement with Dyson's bid than others.
The effort to expedite the approval of Dyson's ventilators was criticized for a lack of understanding of safety risks, contrasting urgency with prudent oversight.
Gove denied any intention to bypass the regulatory framework and emphasized the untenability of a minister prioritizing deadlines over safety in healthcare.
Eyewitness accounts recounted the pressure from Gove’s office, which sought MHRA approval for Dyson's product despite acknowledging potential safety risks.
Gove admitted to having more involvement with Dyson’s bid than other applicants, yet firmly stated he could not dictate regulatory approvals.
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