Cheryl Grainger Exposes MHRA Pregnancy Data Fight | Stellify Podcast episode artwork

EPISODE · Mar 16, 2026 · 1H 44M

Cheryl Grainger Exposes MHRA Pregnancy Data Fight | Stellify Podcast

from Stellify Podcast · host Ant Critchley

In this episode of the Stellify Podcast, Ant Critchley sits down with Cheryl Grainger, a pharmaceutical training consultant who spent decades teaching within the pharmaceutical industry about clinical trials, immunology, pharmacology and drug development.During the COVID era Cheryl began asking questions about the scientific and regulatory processes surrounding the vaccine rollout. What followed was a two-year legal battle with the UK medicines regulator (MHRA) to obtain data relating to pregnancy outcomes and adverse reactions.In this conversation Cheryl explains:• Her background inside the pharmaceutical industry• Why the COVID response raised serious scientific concerns for her• Her Freedom of Information requests to the MHRA• The tribunal process to obtain pregnancy monitoring data• What the Yellow Card Vaccine Monitor revealed• How regulators interpret safety data• Why transparency and scientific scrutiny matter in public health decisionsAnt opens the episode with a personal tribute to a friend who recently passed away, highlighting why conversations around medical transparency and patient safety remain important.This episode aims to create space for open dialogue about science, regulation and accountability, allowing listeners to explore the evidence and form their own conclusions.00:00 Tribute and opening message03:45 Introducing Cheryl Grainger06:10 Cheryl’s background in the pharmaceutical industry12:30 Why the COVID response raised scientific concerns20:15 Understanding the MHRA and regulatory oversight29:40 The Freedom of Information requests begin40:05 The two-year tribunal battle for pregnancy data52:00 The Yellow Card Vaccine Monitor explained01:06:40 Serious adverse reactions and data interpretation01:18:00 Why Cheryl believes transparency is essential01:33:00 The broader questions around pharmaceutical regulation01:42:00 Final thoughts and reflections on accountability---Join the Stellify Community! Dive deeper into hidden truths, shadow work, and spiritual awakening — free + exclusive member content now live!Visit: https://www.becomingstellify.co.ukJoin the FREE private community: https://www.patreon.com/becomingstellifyLet’s awaken and rise — together.Join this channel to get access to perks:https://www.youtube.com/channel/UCzTHjL5iaMZwuW2YVkKqkjw/joinI would be extremely grateful if you bought me a coffee to support the work I do : https://buymeacoffee.com/stellifyJoin this channel to get access to perks:https://www.youtube.com/channel/UCzTHjL5iaMZwuW2YVkKqkjw/join

In this episode of the Stellify Podcast, Ant Critchley sits down with Cheryl Grainger, a pharmaceutical training consultant who spent decades teaching within the pharmaceutical industry about clinical trials, immunology, pharmacology and drug development.During the COVID era Cheryl began asking questions about the scientific and regulatory processes surrounding the vaccine rollout. What followed was a two-year legal battle with the UK medicines regulator (MHRA) to obtain data relating to pregnancy outcomes and adverse reactions.In this conversation Cheryl explains:• Her background inside the pharmaceutical industry• Why the COVID response raised serious scientific concerns for her• Her Freedom of Information requests to the MHRA• The tribunal process to obtain pregnancy monitoring data• What the Yellow Card Vaccine Monitor revealed• How regulators interpret safety data• Why transparency and scientific scrutiny matter in public health decisionsAnt opens the episode with a personal tribute to a friend who recently passed away, highlighting why conversations around medical transparency and patient safety remain important.This episode aims to create space for open dialogue about science, regulation and accountability, allowing listeners to explore the evidence and form their own conclusions.00:00 Tribute and opening message03:45 Introducing Cheryl Grainger06:10 Cheryl’s background in the pharmaceutical industry12:30 Why the COVID response raised scientific concerns20:15 Understanding the MHRA and regulatory oversight29:40 The Freedom of Information requests begin40:05 The two-year tribunal battle for pregnancy data52:00 The Yellow Card Vaccine Monitor explained01:06:40 Serious adverse reactions and data interpretation01:18:00 Why Cheryl believes transparency is essential01:33:00 The broader questions around pharmaceutical regulation01:42:00 Final thoughts and reflections on accountability---Join the Stellify Community! Dive deeper into hidden truths, shadow work, and spiritual awakening — free + exclusive member content now live!Visit: https://www.becomingstellify.co.ukJoin the FREE private community: https://www.patreon.com/becomingstellifyLet’s awaken and rise — together.Join this channel to get access to perks:https://www.youtube.com/channel/UCzTHjL5iaMZwuW2YVkKqkjw/joinI would be extremely grateful if you bought me a coffee to support the work I do : https://buymeacoffee.com/stellifyJoin this channel to get access to perks:https://www.youtube.com/channel/UCzTHjL5iaMZwuW2YVkKqkjw/join

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Cheryl Grainger Exposes MHRA Pregnancy Data Fight | Stellify Podcast

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This episode was published on March 16, 2026.

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In this episode of the Stellify Podcast, Ant Critchley sits down with Cheryl Grainger, a pharmaceutical training consultant who spent decades teaching within the pharmaceutical industry about clinical trials, immunology, pharmacology and drug...

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