An adverse event (AE) is any unintended medical occurrence in a patient or clinical trial participant who has been given a pharmaceutical product, supplement, medical device, or treatment-regardless of whether it is causally related to that product or treatment.
Pharm-D is committed to ensuring the safety and quality of our products. If you have experienced an adverse event, have a product-related enquiry, or wish to report a complaint, please complete the form below.
Your report helps us monitor product performance and take appropriate action where necessary.
Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.
Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.
Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.
Once submitted, our Regulatory/ Quality/ Pharmacovigilance team will review your report. You may be contacted for additional information. We aim to respond within 3 working days.
