Please include data about NHS use of biocides as sealer's when mercury amalgam was used in 1996

Medicines and Healthcare Products Regulatory Agency did not have the information requested.

Dear Medicines and Healthcare products Regulatory Agency,

Please provide details about the physical and chemical/metal/alloy properties of Mercury amalgam used by the NHS in 1996 as a restorative material in dental surgical procedures.

Please include data about NHS use of biocides as sealer's when mercury amalgam was used in 1996:

1.The name of manufacturer(s)
2.The name of each substance in the product including the name of it's active substance and the amount of each substance as a percentage of the whole.
3.The classification of the biocidal/heavy metal/alloy product.
4.Particulars of any likely direct or indirect adverse side
effects.
5.Procedures to be followed and measures to be taken in the case of spillage or leakage of the biocidal product and the active substance contained in that biocidal product.
6. Safety data sheets for mercury amalgams and
biocidal/paraformaldehyde based sealer's.
7. Data and registry of recorded adverse acute and chronic ill health associated with mercury amalgams and/or any other dental medical materials and substances.
8. Please list all biocides and heavy metals and alloys used today in the NHS as dental restorative materials and sealer's.

Kind regards

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
results of which will be published on our Customer Services webpage in
early 2014. 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:
[11]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
 

This email and any files transmitted with it are confidential. If you are
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If you are not the intended recipient, please notify the sender
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Communications via the GSi may be automatically logged, monitored and/or
recorded for legal purposes.

References

Visible links
1. http://www.mhra.gov.uk/Contactus/Custome...
2. http://www.mhra.gov.uk/Howweregulate/Med...
3. http://www.mhra.gov.uk/Howweregulate/Dev...
4. http://www.mhra.gov.uk/Howweregulate/Med...
5. http://www.mhra.gov.uk/Howweregulate/Dev...
6. http://www.mhra.gov.uk/Safetyinformation...
7. http://www.mhra.gov.uk/Safetyinformation...
8. http://www.mhra.gov.uk/Howweregulate/Med...
9. http://www.mhra.gov.uk/Safetyinformation...
10. http://www.mhra.gov.uk/Safetyinformation...
11. https://www.surveymonkey.com/s/MHRACusto...

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 14/100
       
Dear Granito,
       
RE:  REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000
       
Thank you for your enquiry which we received on 10 March 2014. 
       
I confirm that your request is being handled under the Freedom of Information Act and you should receive a reply within 20 working days from our date of receipt.

If you need to contact us again about this request, please quote the reference number above.
       
Kind Regards,

Customer Services
External Relations
Medicines and Healthcare Products Regulatory Agency
Tel: 020 3080 6000

show quoted sections

Dear MHRA Customer Services,

Thank you for your time.

Kind regards

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
results of which will be published on our Customer Services webpage in
early 2014. 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:
[11]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
 

This email and any files transmitted with it are confidential. If you are
not the intended recipient, any reading, printing, storage, disclosure,
copying or any other action taken in respect of this email is prohibited
and may be unlawful.

 

If you are not the intended recipient, please notify the sender
immediately by using the reply function and then permanently delete what
you have received.Incoming and outgoing email messages are routinely
monitored for compliance with the Department of Healths policy on the use
of electronic communications.

 

For more information on the Department of Healths email policy, click

http://www.dh.gov.uk/DHTermsAndCondition...

show quoted sections

Communications via the GSi may be automatically logged, monitored and/or
recorded for legal purposes.

References

Visible links
1. http://www.mhra.gov.uk/Contactus/Custome...
2. http://www.mhra.gov.uk/Howweregulate/Med...
3. http://www.mhra.gov.uk/Howweregulate/Dev...
4. http://www.mhra.gov.uk/Howweregulate/Med...
5. http://www.mhra.gov.uk/Howweregulate/Dev...
6. http://www.mhra.gov.uk/Safetyinformation...
7. http://www.mhra.gov.uk/Safetyinformation...
8. http://www.mhra.gov.uk/Howweregulate/Med...
9. http://www.mhra.gov.uk/Safetyinformation...
10. http://www.mhra.gov.uk/Safetyinformation...
11. https://www.surveymonkey.com/s/MHRACusto...

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Dear Granito,
 
Enquiry under the Freedom of Information Act (2000) – MHRA Ref: FOI 14/100
 
Please see below our response to your specific questions:
 
Please provide details about the physical and chemical/metal/alloy
properties of Mercury amalgam used by the NHS in 1996 as a restorative
material in dental surgical procedures.
The MHRA does not hold this information
 
Please include data about NHS use of biocides as sealer's when mercury
amalgam was used in 1996:
 
1.The name of manufacturer(s)
The MHRA does not hold this information.
 
2.The name of each substance in the product including the name of it's
active substance and the amount of each substance as a percentage of the
whole.
The MHRA does not hold this information.
 
3.The classification of the biocidal/heavy metal/alloy product.
Dental amalgams are classified as Class IIa medical devices.
 
4.Particulars of any likely direct or indirect adverse side effects.
The MHRA does not hold this information.
 
5.Procedures to be followed and measures to be taken in the case of
spillage or leakage of the biocidal product and the active substance
contained in that biocidal product.
The MHRA does not hold this information.
 
6. Safety data sheets for mercury amalgams and biocidal/paraformaldehyde
based sealer's.
The MHRA does not hold this information.
 
7. Data and registry of recorded adverse acute and chronic ill health
associated with mercury amalgams and/or any other dental medical materials
and substances.
The MHRA has not received any medically confirmed adverse acute or chronic
ill health associated with mercury amalgams and/or any other dental
medical materials and substances.
 
8. Please list all biocides and heavy metals and alloys used today in the
NHS as dental restorative materials and sealer's.
The MHRA does not hold this information.
 
If you have a query about this email, please contact the MHRA. If you are
unhappy with our decision, you may ask for it to be reviewed. That review
will be undertaken by a senior member of the Agency who has not previously
been involved in your request. If you wish to pursue that option please
write to the Communications Directorate, 4th Floor, Medicines and
Healthcare Products Regulatory Agency, 151 Buckingham Palace Road,
Victoria, London, SW1W 9SZ at the above address quoting the above
reference.
After that, if you remain dissatisfied, you may ask the Information
Commissioner at:
 
The Information Commissioner's Office
Wycliffe House
Water Lane
Wilmslow
Cheshire
SK9 5AF
 
to make a decision on whether or not we have interpreted the FOIA
correctly in withholding information from you.
 
Yours Sincerely,
Customer Services
External Relations
Medicines and Healthcare products Regulatory Agency
Tel: 020 3080 6000
 
 
 
 

show quoted sections

Dear MHRA Customer Services,

1. Who or what agency does have the information requested by me?

2. If it is not the HSE then what other agency because they sent me to you?

3. Are not Government ministers supposed to legally sign off all drug and medicine licenses in order for them to be deemed safe and tested for public use?

4. How do you know how these toxic materials are impacting on public health if you do have a national register such the 1 now being put in place by Dr Poulter & Jeremy Hunt after faulty breast implants caused chronic ill health in a number of women in the UK?

Thank you for your time

Granito

Yours sincerely,

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
result is now published on our Customer Services webpage at
[11]http://www.mhra.gov.uk/Contactus/Custome.... 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:
[12]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
Our offices are currently closed for the public holiday on 5 May 2014 and
we will re-open on Tuesday 6 May 2014 at 9am. 
 
 
 

show quoted sections

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Dear Granito,
       
Thank you for your email of 5 May 2014.

We are sorry we are unable to assist with your enquiry and would suggest that you contact the General Dental Council (GDC) who may be able to assist or signpost you. Their contact details are below:

Email: [email address]
Tel: +44 20 7887 3800
       
Yours Sincerely,

Customer Services
External Relations
Medicines and Healthcare products Regulatory Agency
Tel: 020 3080 6000

show quoted sections

Dear MHRA Customer Services,

Thank you for your reply. However, the General Dental Council was the first agency I contacted in 2011. It's supposed 'investigations' were pathetically lacking and i was informed that if i wanted data about medical devices used by a previous NHS dentist I would have to take civil action to get it! Now that is not right is it?

The GDC relied on incomplete record keeping of vital data and my dental records were refused until the GDC got involved at my request. Although, it was a complete waste of time and the only people they are protecting is the dentists. It seems that when the public [myself]wish to hold government to account they [[me] are treated with contempt. So it appears my concerns have come full circle, which is no surprise as this is a common way of denying the public data which is currently secret [if it exists at all]. Why should I have to take out civil action in court to find out what 'medical devices' ( mercury/a highly toxic hazardous material) was used to treat me? In light of the Minamata Treaty, which states:

'Significantly, this treaty includes a specific article related to human health (Article 16) with measures and activities that can be undertaken to assess and protect human health from mercury. It outlines an important requirement that information related to mercury and human health must not be kept confidential thereby underscoring the public Right To Know about mercury impacts on their health.'

The related health clause under Article 17 which concludes, “For the purposes of this Convention, information on the health and safety of humans and the environment shall not be regarded as confidential” may provide leverage for those who wish to seek information from government on known sources and impacts of mercury on men, women and children in the UK. Information that has previously been classified may be released and publicised, raising awareness about mercury pollution in communities.

The hazards associated with mercury added products cannot be underestimated. The potential for mercury to be released at every stage from manufacture through useful life and disposal phase means that the potential for exposure during daily use of these products is high.

Thank you for your time,

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
result is now published on our Customer Services webpage at
[11]http://www.mhra.gov.uk/Contactus/Custome.... 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:
[12]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
 
 

show quoted sections

Dear Medicines and Healthcare products Regulatory Agency,

Please pass this on to the person who conducts Freedom of Information reviews.

I am writing to request an internal review of Medicines and Healthcare products Regulatory Agency's handling of my FOI request 'Please include data about NHS use of biocides as sealer's when mercury amalgam was used in 1996'.

[I wish to see proof of safety for mercury amalgam and biocidal sealer's used routinely by the NHS and what exactly was being used as restorative material in 1996 in NHS hospitals and NHS dentists ]

A full history of my FOI request and all correspondence is available on the Internet at this address: https://www.whatdotheyknow.com/request/p...

Thank you for your time,

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
result is now published on our Customer Services webpage at
[11]http://www.mhra.gov.uk/Contactus/Custome.... 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:
[12]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
 
 

show quoted sections

Dear Medicines and Healthcare products Regulatory Agency,

Please pass this on to the person who conducts Freedom of Information reviews.

I am writing to request an internal review of Medicines and Healthcare products Regulatory Agency's handling of my FOI request 'Please include data about NHS use of biocides as sealer's when mercury amalgam was used in 1996'.

[ my concerns are not being addressed ]

A full history of my FOI request and all correspondence is available on the Internet at this address: https://www.whatdotheyknow.com/request/p...

Thank you for your time,

Granito

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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 all requests within the Department of Health’s target response
time of 18 working days. Further information on how we handle different
requests can be found on our website at the link below:
 
[1]http://www.mhra.gov.uk/Contactus/Custome...
 
Our website contains a wealth of information which may assist with your
enquiry. Some of our popular pages are:
 
Clinical Trials of medicines:
 
[2]http://www.mhra.gov.uk/Howweregulate/Med...
       
Clinical Trials of medical devices:
 
[3]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Manufacturer’s and wholesale dealer’s licences:

[4]http://www.mhra.gov.uk/Howweregulate/Med...
 
Registration of medical devices, opticians and dental laboratories:

[5]http://www.mhra.gov.uk/Howweregulate/Dev...
 
Reporting a side effect to a medicine:

[6]http://www.mhra.gov.uk/Safetyinformation...
 
Reporting an adverse incident involving a medical device:
 
[7]http://www.mhra.gov.uk/Safetyinformation...
 
Does my product need a licence?:

[8]http://www.mhra.gov.uk/Howweregulate/Med...
 
Reporting a counterfeit medical product:
 
[9]http://www.mhra.gov.uk/Safetyinformation...
 
Buying medicines over the internet:
 
[10]http://www.mhra.gov.uk/Safetyinformation...
 
We’d like to thank you if you participated in our recent survey, the
result is now published on our Customer Services webpage at
[11]http://www.mhra.gov.uk/Contactus/Custome.... 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:
[12]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
External Relations
Medicines and Healthcare Products Regulatory Agency
 
Please note this is an automated reply; please do not respond to this
message.
 
 
 

show quoted sections

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

2 Attachments

Dear Granito,
       
Thank you for your email.

Attached is the response to your review request.

       
Kind Regards,

Customer Services
External Relations
Medicines and Healthcare Products Regulatory Agency

Tel: 020 3080 6000

 

show quoted sections