Medicines and Healthcare Products Regulatory Agency

An executive agency and a Crown Body, also called MHRA

1135 requests
Make a Freedom of Information request to this authority
Drugs reliance route statistics for the UK
Response by Medicines and Healthcare Products Regulatory Agency to Hin Chan on .

Awaiting classification

Dear Hin Chan, I am writing in response to your request for information, received 23rd May. Please find the response to your request attached. Y...
Medical devices reliance route statistics for the UK
Response by Medicines and Healthcare Products Regulatory Agency to Hin Chan on .

Awaiting classification

Dear Hin Chan, I am writing in response to your request for information, received 23rd May. Please find the response to your request attached. Y...
UK Miscarriage Data
Response by Medicines and Healthcare Products Regulatory Agency to Mark Huxley on .

Awaiting response

MHRA reference: FOI2025/00536 Dear Mark Huxley, Thank you for your information request, which we received on 30 May. We have understood your reque...
Previous decisions about whether an experiment is a CTIMP or a non-CTIMP #3
Response by Medicines and Healthcare Products Regulatory Agency to Will Lawn on .

Awaiting classification

MHRA reference: FOI2025/00605 Dear Will Lawn, Thank you for your information request, which we received on 14 June. We have understood your reques...
Detailed outcome data on the monitored pregnant women during Covid vaccination trial
Response by Medicines and Healthcare Products Regulatory Agency to Rob N on .

Successful

Dear Rob N, I am writing in response to your request for information, received 5th May. Please find the response to your request attached. Yours...
Previous decisions about whether an experiment is a CTIMP or a non-CTIMP #2
Response by Medicines and Healthcare Products Regulatory Agency to Will Lawn on .

Awaiting classification

MHRA reference: IR2025/00598 Dear Will Lawn, Thank you for your request for an internal review of your request FOI2025/00464, which we received on...
Re: ICH S12 Guideline and implementation status
Response by Medicines and Healthcare Products Regulatory Agency to Linda Birr-Pixton on .

Awaiting response

MHRA reference: FOI2025/00593 Dear Linda Birr-Pixton, Thank you for your information request, which we received on 14 June. We have understood you...
Banned drugs for treatment of Covid 19 and reasons
Response by Medicines and Healthcare Products Regulatory Agency to Tom Jefferson on .

Awaiting response

MHRA reference: FOI2025/00574 Dear Tom Jefferson, Thank you for your information request, which we received on 9 June. We have understood your req...
CellAED defibrillator
Response by Medicines and Healthcare Products Regulatory Agency to Kevin Furnish on .

Awaiting classification

Dear Kevin Furnish, I am writing in response to your request for information, received 30th April. Please find the response to your request attach...
Informed consent content to those offered avian influenza H5 vaccines
Response by Medicines and Healthcare Products Regulatory Agency to Tom Jefferson on .

Successful

Dear Tom Jefferson, I am writing in response to your request for information, received 28th March. Please find the response to your request at the...
When did the MHRA classify the Electroconvulsive Therapy devices as a Class II device?
Response by Medicines and Healthcare Products Regulatory Agency to Sarah Price Hancock on .

Awaiting classification

Dear Sarah Hancock, I am writing in response to your request for information, received 31st January. Please find the response to your request atta...
Batch Data Compliance Documentation for Pfizer BNT162b2
Response by Medicines and Healthcare Products Regulatory Agency to Carl Rawlingson on .

Partially successful

Dear Caroline Rawlingson, I am writing in response to your request for information, received 24th April. Please find the response to your request...
Money spent on management consultants
Response by Medicines and Healthcare Products Regulatory Agency to curious on .

Awaiting classification

Dear Customer, Thank you for your request. In order to log this request, we need you to provide us with your name. Once provided, we will be able to...
Production process of influenza seasonal and avian vaccines
Response by Medicines and Healthcare Products Regulatory Agency to Tom Jefferson on .

Partially successful

Dear Tom Jefferson, I am writing in response to your request for information, received 31st March. Please find the response to your request attach...
Previous decisions about whether an experiment is a CTIMP or a non-CTIMP
Response by Medicines and Healthcare Products Regulatory Agency to Will Lawn on .

Refused

Dear Will Lawn, I am writing in response to your request for information, received 31st March. Please find the response to your request attached....
Flash Glucose devices available in 2021?
Response by Medicines and Healthcare Products Regulatory Agency to RBeedham on .

Information not held

Our ref: FOI 23/689   Dear RBeedham,   Thank you for your request of 19 September 2023 under the Freedom of Information Act. You requested:...
Studies for new avian influenza vaccines showing bioequivalence to Aflunov
Response by Medicines and Healthcare Products Regulatory Agency to Tom Jefferson on .

Partially successful

Dear Tom Jefferson, I am writing in response to your request for information, received 29th March. Please find the response to your request attach...
Contact with tobacco industry
Response by Medicines and Healthcare Products Regulatory Agency to Allen Gallagher on .

Refused

Dear Allen Gallagher, I am writing in response to your request for information, received 14th March. Please find the response to your request atta...
EU and UK Health Authority approval
Response by Medicines and Healthcare Products Regulatory Agency to Roni on .

Awaiting classification

Dear Customer All publicly available information on registered devices can be found on our Public Access Registration Database, please utilise this si...
Melatonin switch from GSL to POM 1995
Response by Medicines and Healthcare Products Regulatory Agency to Dr. J.G.C. Omtzigt on .

Information not held

Dear Dr. J.G.C. Omtzigt,   Many thanks for your request for information dated 19 January 2024, where you asked the following: Up until 1995, mel...
F&P SleepStyle Approval
Response by Medicines and Healthcare Products Regulatory Agency to Roni on .

Partially successful

Dear Customer All publicly available information on registered devices can be found on our Public Access Registration Database, please utilise this si...
Regulatory status for novel Microbime Test
Response by Medicines and Healthcare Products Regulatory Agency to Natasha on .

Waiting clarification

Dear Natasha K Thank you for your email. In order to help assist with request we are grateful if you could provide us with your full name and also if...
FOI 21/936-FOI 21/1129 Graphene Oxide in medicines
Response by Medicines and Healthcare Products Regulatory Agency to Bob on .

Waiting clarification

Dear Bob,   Thank you for your email. Section 8 of the FOI Act sets out the requirements for a valid request. One of these is for the requester to...
Request 1089 - Diabetes 2 eyes and Metformin
Response by Medicines and Healthcare Products Regulatory Agency to M Hands on .

Waiting clarification

Dear M Hands, Before we log your request, we need to request further clarification. Please can you clarify what you mean by EU institutions and confi...
Covid vaccine emergency use authorization Update
Response by Medicines and Healthcare Products Regulatory Agency to Katon bouzalakos on .

Partially successful

Dear Katon Bouzalakos, I am writing in response to your request for information, received 13th March. Please find the response to your request att...

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