Here we reproduce a letter written to an MP by a constituent.
The letter raises concerns about the potential risks of approving future mRNA vaccines under a “platform authorisation” model whereby updates are assumed to be safe because the underlying methodology is considered safe – the way seasonal egg based influenza vaccines were regulated. This means the Monkeypox mRNA vaccines and others need not be authorised on a product-specific basis as discussed in a May 2024 MHRA Board meeting, but can piggy back on the claims made about the safety of covid vaccines. What could possibly go wrong?