CAPA is often overlooked as an integral component of a quality system. More often than not, the FDA can trace deficiencies in a system directly back to the CAPA system. However, an effective quality system needs more than just a rework of the outcome of the ineffective CAPA system. It needs a rework of the system itself. 

If you're struggling to get a hold on your CAPA system, need some FDA advice, or want to expand your knowledge on the issue, MassMEDIC and R&Q would like to help you.

MassMEDIC and R&Q will be hosting a "CAPA on CAPA" webinar Sept. 14th, from 12 to 1 p.m EDT and you can register here. The content will be presented by R&Q's own FDA expert Paul Robinson. As Senior Director of Regional Operations, Paul has 25+ years of domestic and international experience, and has maintained more than 20 manufacturing plants worldwide. Read about why he loves working for R&Q in our Boston Employee Spotlight. 

paul robinson regulatory and quality solutions for medical devices

Here's what you will learn in the webinar.

CAPA Regulations/Requirements
820.100
Ready for an audit? What does the FDA look for?

CAPA Process/System
Feeders
Procedures
Data Trending/Evaluation/Alerts
Risk Management
System Management

The CAPA
Root Cause Analysis
Statistical Tools
DELCS
Discipline, Engineering Logic, and Common Sense

Still not convinced? Did we mention free registration with the click of a button? Register now and reserve your spot. To reiterate, CAPA is not simply documentation to prove you've addressed an issue. It is a critical component of your quality system. 

Register for Free

We are passionate about your success. Tell us more about your regulatory and quality needs so we can help.

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