Doc Malik #333 - Safe and Effective? Cheryl Grainger on mRNA, Regulators, and Real Risks
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ABOUT THIS CONVERSATION:
In this episode, I speak with Cheryl, who brings insider experience from the pharmaceutical world and a deeply analytical mind to everything that’s unfolded over the past few years.
We dive into the role of the MHRA, the UK’s drug regulator, and explore whether it’s truly serving public health or merely rubber-stamping products handed to it by pharmaceutical companies. Cheryl shares her concerns about the lack of transparency, the failures of pharmacovigilance, and how freedom of information requests have revealed troubling gaps in regulatory oversight, especially in relation to the COVID-19 vaccine rollout.
We talk about mRNA technology, gene therapy, and the disturbing trend of pushing products to market without adequate long-term safety data. Cheryl also highlights the yellow card system, supposedly in place to track adverse effects, which is shockingly underused and almost unknown to most doctors.
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I hope you enjoy this episode.
Much love, as always.
Doc Malik
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