Contact us

Do you visit us?

Avenue Thomas Edison, 32
1402 Thines (Nivelles)
Belgium 

T : +32 (0)2 374 02 53 
F : +32 (0)2 374 68 81

For any questions regarding nutrivigilance, pharmacovigilance and materiovigilance, please contact us by e-mail : pv@trenker.be 

For any other question :info@trenker.be

Nutrivigilance

Post-marketing surveillance system for dietary supplements.
To report any undesirable side effects, please fill in the following information:

  • Your surname and first name
  • Your identity (pharmacist, doctor, manager of a health food store, wholesaler, user, etc.)
  • The date of the day of reporting
  • A contact email address or telephone number
  • A contact email address or telephone number
  • The name of the dietary supplement concerned + batch no. & expiry date
  • How and when the dietary supplement was taken
  • How long the dietary supplement had been used
  • Any other products taken simultaneously
  • Any information deemed relevant

Pharmacovigilance

Post-marketing surveillance system for pharmaceuticals.
To report any undesirable side effects, please fill in the following information:

  • Your surname and first name
  • Your identity (pharmacist, doctor, user, etc.)
  • The date of birth of the patient 
  • A contact email address or telephone number
  • A contact email address or telephone number
  • The name of the pharmaceutical concerned + batch no. & expiry date
  • How and when the pharmaceutical was taken
  • How long the pharmaceutical had been used
  • Any other products taken simultaneously
  • Any information deemed relevant

Materiovigilance

Post-marketing surveillance system for medical devices.
To report any undesirable side effects, please fill in the following information:

  • Your surname and first name
  • Your identity (pharmacist, doctor, user, etc.)
  • The date of birth of the patient (if you are a pharmacist or a doctor)
  • The date of the notification of the side effect(s)
  • A contact email address or telephone number
  • The name of the medical device concerned + batch no. & expiry date
  • How and when the medical device was taken
  • How long the medical device has been used
  • Any other products taken simultaneously
  • Any information deemed relevant
     

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