USFDA completes inspections at Suven Pharma facilities with no form 483
Hyderabad: Suven Pharma has announced that the US Food & Drug Administration (US FDA) has completed the inspections at the Company's Pashamylaram facilities.The inspection was conducted from February 12, 2024, to February 23, 2024."This is to inform you that our Active Pharmaceutical Ingredients (API) and Formulations facilities (Unit-3 and Unit-5, respectively) in Pashamylaram,...
Hyderabad: Suven Pharma has announced that the US Food & Drug Administration (US FDA) has completed the inspections at the Company's Pashamylaram facilities.
The inspection was conducted from February 12, 2024, to February 23, 2024.
"This is to inform you that our Active Pharmaceutical Ingredients (API) and Formulations facilities (Unit-3 and Unit-5, respectively) in Pashamylaram, Hyderabad, India, have completed the PreApproval Inspections (PAI) and Good Manufacturing Practices (GMP) inspections by the US Food & Drug Administration (US FDA) today," the Company informed in a BSE filing.
Read also: Berhyanda gets DoP nod to acquire up to 76.1 percent stake in Suven Pharma
"We are pleased to inform you that no Form 483 has been issued as a result of the inspection," Suven added.
Read also: Foreign investment of up to Rs 9589 crore in Suven Pharma approved by Cabinet
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/treatment or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2024 Minerva Medical Treatment Pvt Ltd