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Publications and consultations

Welcome to the publications section.

We produce a range of publications, most of which are aimed at healthcare professionals or people working in the device or pharmaceutical industries. Some are available in full text as pdf documents.


Latest publications

07 Feb 2012 | Class 4 Drug Alert: Updated information for our alerts EL(11)A/32 of 21 December 2011 and EL(12)A/01 of 11 January 2012 - EL(12)A/05

Following our alerts EL(11)A/32 issued on 21 December 2011 and EL(12)A/01 issued on 11 January 2012, B.Braun Medical Ltd  have advised us that they need to release additional batches of  the above NuTRIflex Lipid products which may contain particulates and should be subject to the same additional filtration process previously recommended during infusion.

06 Feb 2012 | Monthly list of MDAs 2012

A month-by-month list of Medical Device Alerts that we have issued in 2012.

06 Feb 2012 | Public consultation (ARM 81): Request to reclassify Imodium Instants (loperamide hydrochloride) 12 tablet pack size from Pharmacy (P) to General Sales List (GSL)

Consultation ARM 81 seeks your views on the reclassification of Imodium Instants (loperamide hydrochloride) 12 tablet pack size from Pharmacy (P) to General Sales List (GSL). Comments are invited by 5 March 2012.

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Corporate publications

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This section includes all our corporate publications, including our annual reports, corporate plans, business plans and our framework document.

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Consumer publications

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This section includes publications to provide guidance to consumers on the safe use of medicines and medical devices.
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Safety guidance

Guidance documents

This section includes the wide range of documents we produce which provide guidance on safety issues concerning medicinces and medical devices.

Regulatory guidance

Guidance documents

This section includes the wide range of publications we produce to provide guidance to industry on the regulation of devices and medicines.

Consultations

People being consulted at a meeting
The MHRA formally consults organisations representing public and professional interests, trade associations and industry on proposed statutory changes and other matters of importance.

Public Assessment Reports (PARs)

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The MHRA makes assessment reports available for all new licences for medicines granted after 30 October 2005, albeit with commercially or personally confidential information removed.

Posters and leaflets

Nurse looking at a leaflet with a patient
This section includes our range of posters and leaflets which complement our more comprehensive guidance documents.
Page last modified: 12 July 2011