Biocon gets EU GMP certification for Bengaluru drug product facility

Published On 2018-07-07 05:00 GMT   |   Update On 2018-07-07 05:00 GMT

New Delhi: Biotechnology major Biocon said it has received EU GMP certification for its sterile drug product manufacturing facility in Bengaluru.


The facility was inspected by the European agencies in March 2018, Biocon said in a filing to BSE.


"This facility is used for the manufacture of Biocon's portfolio of biosimilars," a company spokesperson said.


Earlier in May, in a regulatory filing, Biocon had said it had received a preliminary report from the European Regulator post inspection of its sterile drug product facility in Bengaluru in March 2018.


"The report lists six major observations with no observation classified as critical. We will submit a corrective and preventive action plan to the European inspection agency within the stipulated time period," a company spokesperson had said.

Article Source : PTI

Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News