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Blog MHRA Inspectorate
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Medicines and Healthcare products Regulatory Agency
MHRA Inspectorate

Michelle Yeomans

I joined the Inspectorate in 2005 and have worked across the GXP teams as an Inspector, Senior Inspector and GMDP Operations Manager. In October 2017, I took on a full time project based role focusing on business process improvement and to lead the Inspectorate inputs to the Agency's Operational Transformation Programme and Digital Transformation projects going forward.

Inspector Recruitment – Part Two

Posted by: , Posted on: - Categories: Good clinical practice, Good distribution practice, Good laboratory practice, Good manufacturing practice, Good pharmacovigilance practice, Inside the Inspectorate, Wider MHRA

In part 1 of the inspectorate recruitment posts, we provided information on the inspector role and recruitment process, part 2 provides more information on the benefits and opportunities available to MHRA inspectors.

Inspector Recruitment -Part One

Posted by: , Posted on: - Categories: Good clinical practice, Good distribution practice, Good laboratory practice, Good manufacturing practice, Good pharmacovigilance practice, Inside the Inspectorate, Wider MHRA
A plaque with the words 'Come in we're hiring'

Have you ever thought about becoming an MHRA inspector but wanted to know more about the role, the application process, or the benefits associated with joining a talented and dynamic team protecting public health? Part one of this two-part blog will hopefully give you the information you need to consider for applying for future roles.

Transitional QPs for Investigational Medicinal Products (IMPs) - Update

Posted by: , Posted on: - Categories: Compliance matters, Good clinical practice, Good manufacturing practice
QP update

We are aware there is some concern for UK business and personal careers, over the status of transitional QPs that were recognised under the transitional arrangements provided in SI 2004/1031, when the Clinical Trials Directive was implemented in 2004. The …

Notification to MS licence holders due to compliance concerns

Posted by: , Posted on: - Categories: Compliance matters, Good manufacturing practice
Dropper dropping liquid into a bottle

In January 2015, MHRA published guidance to ‘specials’ manufactures, to provide an interpretation of the good manufacturing practice (GMP) requirements for specials manufacturers. The GMDP Inspectorate have been concerned that some Specials manufacturers have not always been receiving written orders …

Transitional QPs for investigational medicinal products (IMPs)

Posted by: , Posted on: - Categories: Compliance matters, Good clinical practice, Good manufacturing practice
QP using laptop in office

We are aware there is some concern for UK business and personal careers, over the status of transitional QPs that were recognised under the transitional arrangements provided in SI 2004/1031, when the Clinical Trials Directive was implemented in 2004. The …

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This blog shares the work of the Medicines and Healthcare products Regulatory Agency (MHRA) Inspectorate, by inspectors and those the Inspectorate works with.

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