Bio-med remains very vigilant towards Pharmacovigilance activities which are related to the detection, assessment, understanding & prevention of adverse event (AE)/Adverse drug reaction (ADR) or any other vaccine related problems to ensure safety of vaccine & its uses throughout the lifecycle. Thus Biomed is keen in continuous monitoring and management of the safety profile of all its products through its drug safety data collection worldwide.

All consumers or patients are thus advised to contact their doctor or healthcare professionals in case of any emergency caused due to use of vaccines manufactured by Biomed.

Customers/Healthcare Professionals can report ‘Any Adverse Events / Side Effects’ and/or product quality complaints experienced with BIO-MED Products and report to us vide links below:

Download Post marketing Surveillance (PMS Form) to fill and send by Email/ Courier/ Post

Download offline AEFI reporting Form to fill and send by Courier/Post/Email

More Information on Pharmacovigilance terminologies and Biomed’s policy on the same


For Offline Form Submission :  After completion of reporting form you can submit it to our email or

You can also fax us on – 0120-4340219 . On successful submission, you will get an acknowledgement on your email address.

Procedures for Reporting Side Effects and AEFI


Company information

Bio-Med (P) Limited was established with an abiding faith in the wisdom enshrined in the age-old saying………….
“Prevention is better than cure”
It was with this objective that Bio-Med embarked on its noble mission of producing world-class vaccines essential to the needs of a developing country-India.