Bio-med remains very vigilant towards Pharmacovigilance activities which are related to the
detection, assessment, understanding & prevention of adverse events (AE) / adverse drug
reactions (ADR) or any other vaccine-related problems to ensure safety of vaccines and their
use throughout the lifecycle.

Consumers or patients are advised to contact their doctor or healthcare professionals
in case of any emergency caused due to the use of vaccines manufactured by Biomed. /p p Customers / Healthcare Professionals can report any adverse events, side effects,
and/or product quality complaints using the links below:

Download Post Marketing Surveillance (PMS) Form

Download Offline AEFI Reporting Form

More Information on Pharmacovigilance & Biomed Policy

For Offline Form Submission:
Email:
pharmacovigilancebm@gmail.com |
saryugarg@yahoo.com
Fax: 0120-4340219
You will receive an acknowledgement on successful submission.