Pharmacovigilance

Report

Monitor

Analyze

Comply

Protect

Adverse Event Reporting

Collecting and documenting adverse drug reactions, safety concerns, and product quality complaints from healthcare professionals and patients.

Safety Monitoring

Continuously monitoring local and global safety data to identify potential risks and emerging safety signals throughout a product's lifecycle.

Regulatory Compliance

Ensuring timely safety reporting and full compliance with pharmacovigilance regulations and reporting requirements.

Patient Safety

Evaluating risks, implementing mitigation strategies, and promoting the safe and effective use of medicines to protect patient health.

If you wish to directly notify us about a suspected adverse reaction related to our drugs, please fill in the form below:

Or you can download the yellow form, fill up and send us at- pv@zascorporation.com

24X7 Pharmacovigilance (PV) Contact Number: +880 1888-816936

Pharmacovigilance

Person Details (Who filled up the form):

Patient Details (Who experienced the adverse event):

Product Details

In processing your personal data, ZAS Corporation will fully comply with internationally recognized standards of data protection. In doing so, ZAS Corporation ensures compliance of its staff with strict standards of security and confidentiality.