Pharmacovigilance (according to WHO) is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem. This concerns intolerance to drugs, misuse or abuse, therapeutic errors, drug dependence, antibiotic resistance, therapeutic failure, effects on pregnant women or effects on children…
In the same way, materiovigilance makes it possible to prevent incidents and risks of serious incidents involving medical devices from occurring or reoccurring, by taking appropriate preventive and/or corrective measures.
At Arwa Medic, patient safety is our priority. This is ensured through the monitoring and management of product-related adverse events, which are reported by healthcare professionals and patients.
This monitoring allows us to measure the effectiveness of a medicine and to promote its rational use. We contribute to this by educating, training and awareness of the involved parties.
The scientific and regulatory monitoring that we carry out at Arwa Medic allows us to collect information and pharmacovigilance cases that are recorded and processed by our teams within the regulatory timeframe, in agreement with Health Authorities.
We therefore place at your disposal, the declaration form below.We invite you to fill it in if you wish to report an adverse event.