Effective Preparation for Audits and Inspections in a Regulated Environment (FDA Validation)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Nov 17, 2011 End Date/Time: Nov 17, 2011
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Why Should You Attend:

Many companies fail to prepare adequately for regulatory audits. Since inspectors can also appear unannounced, it is imperative to develop a compliance mindset so your facility is ready at all times for audits.

Are you prepared for a surprise inspection?
Do your employees know how to conduct themselves during an audit?
Are you confident in your ability to respond to difficult questions related to your manufacturing process?
Successful inspections require a well-thought out strategy and employees specifically trained on how to handle such inspections.

This webinar will teach specific techniques to ensure your organizations are ready for regulatory inspections. We will focus on ideas that will help identify areas of improvement before the formal inspection occurs. Further, you will learn techniques that will enhance your effectiveness during the audit execution. We will also examine applicable warning letters and 483s so that your company doesn’t make the same mistakes as other organizations. By building compliance into every aspect of your operation, you can concentrate on getting more quality product out the door.


Online Event
2600 E. Bayshore Road
Palo Alto
United States