Faculty: Kenneth Christie
A successful audit is dependent on understanding what we could expect from regulators. This can be observed by looking at the focus of recent inspections within the industry. Such case studies will help companies to analyze their own practice and address similar issues in advance. This ensures we will be better prepared for an FDA audit resulting in fewer errors. Furthermore, audit techniques used by the FDA has evolved over the years, anticipating what to expect helps to establish a more focused training program as part of the preparation. This 90 minute online session will focus on the changes in FDA Audit Practices and the current method used to determine audit frequencies by using a system of risk assessments. The word – “AUDIT” creates anxiety for the pharma, biotechnology and medical devices industry. This intensifies if you are unaware of how your company’s practices and procedures compare to the rest of the industry. Understanding the most valid regulations, the audit approaches used by regulators, and the common areas of industry deficiencies are part of getting through a successful regulatory inspection. In addressing all these key elements,
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