Factor VIII Aplication 84/85

JJ Evans made this Rhyddid Gwybodaeth request to Commission on Human Medicines

This request has been closed to new correspondence from the public body. Contact us if you think it ought be re-opened.

Gwrthodwyd y cais gan Commission on Human Medicines.

Dear Commission on Human Medicines,

Please supply copies of all Factor VIII Product License Applications received in 1984 & 1985. Many Thanks,

Yours faithfully,

JJ Evans

MHRA Customer Services, Commission on Human Medicines

Dear Enquirer,
 
Thank you for your enquiry to the Medicines and Healthcare products
Regulatory Agency. This automated response confirms that we have received
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If you have not heard from us after 18 working days then please contact us
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Kind regards
 
The Customer Services Team
Communications division
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU
Telephone: 020 3080 6000
Email: [8][Commission on Human Medicines request email]
Stay connected: [9]mhra.gov.uk/stayconnected
 
Please note this is an automated reply; please do not respond to this
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dangos adrannau a ddyfynnir

Dear Commission on Human Medicines,

I hope you are well. This is a reminder that a response to this FOI request is due today. Many Thanks,

Yours faithfully,

JJ Evans

MHRA Customer Services, Commission on Human Medicines

Dear Enquirer,
 
Thank you for your enquiry to the Medicines and Healthcare products
Regulatory Agency. This automated response confirms that we have received
your email and that it will be dealt with as quickly as possible.
 
You can expect a reply from us within a few days for a straightforward
request, however where a more detailed response or contribution from a
specialist is required this is likely to take longer.  We endeavour to
respond to requests within the Department of Health’s target response time
of 18 working days; or 20 working days if your request is a Freedom of
Information request; one month if you are making a request for access to
your personal data under the General Data Protection Regulation 2018.
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical trials of medicines and Clinical investigation for a medical
device:

[1]https://www.gov.uk/medicines-medical-dev...
       
Manufacturer’s and wholesale dealer’s licences:

[2]https://www.gov.uk/apply-for-manufacture...
 
Registration of medical devices, opticians and dental laboratories:

[3]https://www.gov.uk/register-as-a-manufac...
 
Reporting a problem with a medicine or medical device:

[4]https://www.gov.uk/report-problem-medici...
 
Deciding if your product is a medicine or a medical device:

[5]https://www.gov.uk/decide-if-your-produc...
 
Reporting a counterfeit medical product:
 
[6]https://yellowcard.mhra.gov.uk/counterfe...
 
We are continuously looking to make improvements to the service offered by
our Customer Services team, so if you have any feedback please don’t
hesitate to get in touch with us either on the number below or by
completing the form at the link below:
[7]https://www.surveymonkey.com/s/MHRACusto...
 
If you have not heard from us after 18 working days then please contact us
on 020 3080 6000.
 
Kind regards
 
The Customer Services Team
Communications division
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU
Telephone: 020 3080 6000
Email: [8][Commission on Human Medicines request email]
Stay connected: [9]mhra.gov.uk/stayconnected
 
Please note this is an automated reply; please do not respond to this
message.
 
 
 

dangos adrannau a ddyfynnir