1

General Enquiries

Contact Information

📞
📠
Fax
+383 38 721 214
📍
Address
Rr. Marigona Residence
10500 Preoce, Graçanicë
Republic of Kosovo

Office Hours

Monday – Friday08:00 – 16:00
SaturdayClosed
SundayClosed

Activities

⚠️

Për çdo informacion ose shqetësim në lidhje me sjelljen e keqe, mund të na kontaktoni në +383 38 721 212 ose office@meditech-ks.com.
For any information or concerns regarding misconduct, please contact us using the details above.


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Pharmacovigilance / Farmakovigjilenca

Regulatory Affairs & Pharmacovigilance Department

Report an Adverse Event / Raporto një Efekt Anësor

Meditech SH.P.K. is committed to monitoring the safety of all medicinal products it represents. Safety information may be reported at any time — 24 hours a day, 7 days a week.

📱
Mobile (24/7)
📍
Address
Marigona Residence, 10500 Preoce – Graçanicë, Kosovo
Available 24 hours a day, 7 days a week / E disponueshme 24/7

What to Report

  • Adverse events (side effects)
  • Lack of efficacy
  • Overdose
  • Medication errors
  • Exposure in pregnancy
  • Misuse or abuse
  • Quality complaints

Çfarë të Raportohet

  • Efektet anësore
  • Mungesa e efikasitetit
  • Mbidozimi
  • Gabime në përdorim
  • Ekspozimi gjatë shtatzënisë
  • Keqpërdorimi
  • Ankesa për cilësinë

Who Can Report

  • Patients / Pacientët
  • Healthcare Professionals
  • Pharmacists / Farmacistët
  • Caregivers / Kujdestarët
  • Distributors
  • Any other reporter

Adverse Event Report Submitted

Your reference number is:

Please save this number. Our Pharmacovigilance Department will process your report in accordance with applicable regulations.

Adverse Event Report Form


📎

Click to upload or drag and drop

PDF, Word, Excel, Images — max 10MB

🔒 Pharmacovigilance Privacy Notice — PV-PRN-001 | v1.0 | 01.07.2026 Personal data collected during PV activities are processed solely for pharmacovigilance purposes.

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Report a Concern / Raporto një Shqetësim

🔒

Whistleblower Channel — Kanali i Sinjalizimit

Meditech SH.P.K. is committed to the highest standards of business ethics and compliance. This channel allows employees, contractors, suppliers, business partners and any third parties to report concerns confidentially and securely.

Implemented in accordance with Law No. 06/L-085 on Protection of Whistleblowers (Republic of Kosovo).

🛡

No Retaliation

Meditech strictly prohibits any retaliation against individuals who report concerns in good faith.

👤

Anonymous Option

You may submit a report anonymously. Your identity is never required unless you choose to provide it.

Response Time

All reports are acknowledged within 5 business days and investigated within 15 business days.

Report Submitted Successfully

Your case reference number is:

Please save this number. You will receive an acknowledgment within 5 business days and a substantive response within 15 business days.

Whistleblower Report Form
📎

Click to upload or drag and drop

PDF, Word, Excel, Images — max 10MB



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General Contact Form / Formulari i Kontaktit

Send us a message / Dërgoni një mesazh
Name
Meditech SH.P.K. — Regulatory Affairs

Pharmacovigilance / Farmakovigjilenca

1

Report an Adverse Event

Meditech SH.P.K. is committed to monitoring the safety of the medicinal products it represents. If you or a patient have experienced an adverse event, please report it as soon as possible.

2

What Should Be Reported?

  • Adverse Events (Side Effects)
  • Lack of efficacy
  • Overdose
  • Medication errors
  • Exposure during pregnancy
  • Misuse or abuse
  • Product quality complaints
3

How to Report?

Pharmacovigilance Department
📱
Mobile (24/7)
📍
Address
Marigona Residence, 10500 Preoce – Graçanicë, Kosovo
Available 24/7
4

Reporting Availability

Safety reports are accepted 24 hours a day, 7 days a week. Reports received outside business hours will be processed in accordance with Meditech PV procedures and applicable regulatory requirements.
5

Privacy Notice

🔒

Personal data collected during pharmacovigilance activities are processed solely for PV purposes in accordance with applicable data protection legislation. Document: PV-PRN-001 | v1.0 | 01.07.2026

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Why Report?

You do not need to be certain that the medicinal product caused the adverse event before reporting. Every report helps identify potential risks and ensures the safe and effective use of medicines for all patients.