#333 - Safe and Effective? Cheryl Grainger on mRNA, Regulators, and Real Risks

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About this episode:
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.

We discuss the rise in disability claims, the blurred line between drug innovation and reckless experimentation, and how public health is being steered by corporate interests and political agendas rather than genuine medical ethics.

Cheryl speaks calmly, rationally, and with facts to back her concerns. This isn’t about hysteria, it’s about truth, informed consent, and demanding accountability from the very institutions we’re told to trust.

If you think the system is broken, this episode might help you understand why.

I hope you enjoy this episode.

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Much love, as always.

Doc Malik

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About Doc Malik:Orthopaedic surgeon Ahmad Malik is on a journey of discovery when it comes to health and wellness. Through honest conversations with captivating individuals, Ahmad explores an array of topics that profoundly impact our well-being and health

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