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:

Online Side effects (SE) reporting form

Online Adverse effect following immunization (AEFI) reporting form

Download offline Side effects reporting form to fill and send by Courier/Post/Email/Fax

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

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 pharmacovigilancebm@gmail.com or saryugarg@yahoo.com

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

Procedures for PSUR

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.