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Pass Your Medical Device Audit with Confidence

When the auditor comes knocking on your door, will you be ready?

For medical device manufacturers, surviving an audit can be nerve-racking. In the back of your mind, you know the stories of how companies on the FDA watch-list frighten away potential customers and investors. And you’re not alone. The audit process can be scary for established medical device companies too.

On Tuesday, April 4, join Apical Instruments’ Director of Regulatory Affairs/Quality Assurance Kim Khoe and Arena’ Director of Compliance Yelena Bolton for a webinar that will walk you through a real-world example of how to pass an audit exam with flying colors.

In this 45 minute webinar, you’ll learn:

• How to show the auditor you do what you say

• How Arena helps medical device companies with FDA compliance and audits

• How product-centric QMS solutions enable medical device companies to achieve and maintain regulatory compliance and reduce project/compliance cost

We are a huge fan of Apical’s brilliant Kim Khoe whom we are thrilled to be having speak at this webinar. She’ll share how Arena helped streamline Apical Instruments ECO processes, eliminated expensive IT teams, and improved compliance approval success. You’ll also discover how Apical’s ECOs went from months to days and how they saved $10,000 from eliminating manual sharing of files and $100,000 by removing IT costs.

“I always insisted upon Arena,” says Khoe. “Arena can do it all: manage your bill of materials (BOM), quality system, documents, device returns, nonconformance, and your entire CAPA.”

To listen to this webinar, click here.

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