When Risk is Not an Option: A Look at FDA 483's

As pharmaceutical manufacturers continue to develop new technologies and processes become more complex, it's critical to understand the most common regulatory ļ¬ndings to assess and manage risks. Did you know you can you view inspection observations from the Food & Drug Administration (FDA) to help you manage your risks? The FDA’s Office of Regulatory Affairs (ORA) inspection observations are listed on an FDA Form 483. Take a glance at the number of some of their risk findings dating through 2015 for cleaning and microbial control industries at the link below.

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