FDA Issues Statement on Chiron Corporation Inspection
"We are pleased that the Chiron Corporation has taken steps to address issues at their facility in Liverpool as they prepare for the upcoming flu season," said Dr. Jesse Goodman, director of the Center for Biologics Evaluation and Research at the Food and Drug Administration (FDA).
"The letter that we issued to them this week is a positive development and shows significant progress on their part. However, additional work is needed to determine the amount of vaccine Chiron may be able to supply the U.S. market for the upcoming flu season. FDA will evaluate the implementation and effectiveness of their corrective actions going forward. In addition, any vaccine produced must pass all tests for safety and potency before it can be marketed in the U.S."
Source: FDA
IP LifeLine: Keeping it Together When Things Fall Apart: Maintaining Balance When Life Gets Messy
July 25th 2024Balancing personal struggles and professional responsibilities during crises requires self-awareness, self-compassion, healthy boundaries, and support networks. Embrace these strategies to navigate and overcome challenges.
