This week on The Pharmcast, we explore best practices and common pitfalls in FDA 483 Responses.
In 2015, there were an average of 175 inspections and 10 warning letters issued per month by the Center for Devices and Radiological Health alone. Regulatory inspections and 483 findings are a part of being a life sciences company. However, how companies respond can have a major impact on patient safety and business performance.
To share best practices, we held a special presentation with two of our top medical device experts, Victor Chance and Judy Meritz, to outline what they’ve learned over the course of their 20+ year careers in the medical devices industry.
