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Pharmacovigilance
Pharmacovigilance
Risk Management Plans
Our tailored strategies ensure the utmost safety in medical interventions, providing comprehensive insights for healthcare professionals and patients.
Report a Side Effect
Helps us gather real-world data to assess the safety profile of drugs and medical devices post-approval by providing valuable feedback on any adverse effects or unexpected reactions encountered during treatment.
Advanced medicine COLLABORATE WITH THE HEALTH PRACTITIONERS
Advanced medicine COLLABORATE WITH THE HEALTH PRACTITIONERS
To put patient safety in our first priorities
We Advanced medicine collaborate with the health practitioners to put patient safety in our first priorities to provide Integrated health care based on high quality through the concept of Pharmacovigilance which is seeking to monitor, evaluate & prevent any adverse event or any other drug problems through reporting.The Saudi Food & Drug Authorities (SFDA) & Ministry of Health (MOH) in Saudi Arabia & other Competent authority in Gulf Country & All the World have some Legal requirements that control how to deal with the adverse event of medicinal products.
Who can report adverse drug reaction?
Who can report adverse drug reaction?
All health practitioners and members of society can report adverse events.
How to report adverse drug reaction?
How to report adverse drug reaction?
You can use the electronic way through our website and once you click “send”, it will go to pharmacovigilance department in Advanced medicine.Alternatively, contact us through the below details and we will fill the form on behalf of you.
Pharmacovigilance Department
Pharmacovigilance Department
- +966 920001432 Ext. 107
- +966 546030507
- Advancedmedicine@.com
