Pharmacovigilance

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.

Biomed is keen on continuous monitoring and management of the safety profile of all its
products through global drug safety data collection.

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.

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.