INTERESTED IN TILLOMED CIDOFOVIR NON-INTERVENTIONAL POST AUTHORISATION SAFETY STUDY? REGISTER NOW

Contacts

For General Enquiry about the company, contact Tillomed either by :

using the Form opposite or Emailing:

infouk@tillomed.com or customer.service@tillomed.com

Or calling:

 +44 (0)1480 402 400

To speak to the Tillomed Medical Information Team:

 medical.information@tillomed.com

+44 (0)1480 402 400

To Report an adverse event (side effect):

An adverse event (or side effect) is any unwanted medical occurrence in a patient who has been given a pharmaceutical product. This can be any unfavourable and unintended sign, symptom, or disease associated with the use of the product. Adverse events should be reported.

If you experience an adverse event, please inform your healthcare professional straight away.

Adverse event associated with Tillomed product should also be reported to Tillomed. Please report any adverse event to Tillomed using the relevant contact details below. 

 PVUK@tillomed.com

 +44 (0)800 9706115

Please note that Tillomed will not be able to provide medical advice regarding your treatment. Please consult your doctor or pharmacist who are in the best position to advise you about the suitability of a particular treatment.

Our Privacy Policy outlines how Tillomed handles the processing of personal information when dealing with your enquiry, complaint or adverse event report.

    Tillomed are conducting a non-interventional Post Authorisation Safety Study for the safety of Cidofovir through a patient registry. For registration and more details, please refer https://www.cidofovir.com/

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