Pharmacovigilance and drug safety
At Cureviapharma, patient safety is our highest priority. We are committed to ensuring the safe use of the pharmaceutical products we represent. Our Pharmacovigilance and Drug Safety team monitors, evaluates, and manages all information related to the safety of our products, in line with global regulatory standards.
Whats Pharmacovigilance?
Our Commitment
24/7 Safety Monitoring: Continuous surveillance of the products we market to promptly identify and evaluate potential risks.
Reporting Adverse Events: We encourage healthcare professionals, patients, and caregivers to report any side effects or unexpected events related to our products.
Regulatory Compliance: We strictly adhere to local and international pharmacovigilance regulations and collaborate closely with health authorities.
Education & Awareness: We actively provide updated safety information and training to healthcare providers and partners.
Reporting an Adverse Event
If you experience or become aware of any side effect, medical complaint, or issue related to one of our products, please contact our Pharmacovigilance Department immediately.
You can report an adverse event by:
Email: info@cureviapharma.ae
Please provide as much information as possible, including:
Patient initials (if applicable)
Description of the event
Name of the product
Batch number (if available)
Contact details for follow-up
All reports are handled confidentially and in accordance with data protection regulations.
Why Reporting Matters
Your reports help us:
Better understand the safety profile of our products
Update product information when necessary
Protect patients by taking timely actions when needed
Comply with our regulatory obligations