Hacking Risk Management:
3 Ways to Easily Build Risk into Your Processes
Tuesday, October 7th, 11:00 am Pacific / 2:00 pm Eastern
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We hear it all the time in our professional lives – “Risk Management”. We know we need to do it, but often the challenge becomes where to start, and what it all entails. Risk Management and Risk Assessment can be complex for many industries, but it doesn’t have to be. The concepts behind Risk are actually very basic and common to businesses today. Chances are, many compliance professionals are already conducting some level of Risk Assessment and may not even know it.

In this webinar, we are going to dissect the whole concept behind Risk Management and break it down into the most basic terms – “What is the Risk Management process, and how does it factor into existing processes?” Next we will look at three levels in which you can take your processes and enhance them with Risk elements:

Level 1: Decision Trees – We will review the most basic type of Risk Assessment that can easily be managed, tracked and consumed by all personnel.

Level 2: Risk Matrix and Risk Assessments – Taking it a step further, we will look at how you can incorporate more calculated levels of risk that measure multiple factors to give you a systematic and objective decision.

Level 3: Risk Reporting and Trending – Finally, we will look at how Risk can be used not only to help make in-process decisions, but also report and discover trends that can lead more proactive risk-based planning.

Join us on October 7th at 2pm EDT where Glen Fraser, Product Manager for VERSE Solutions will uncover the secrets of Risk Management in Compliance systems, and bring to light all the steps necessary to build Risk into your compliance program. 

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Implementing a CAPA System
Tuesday, September 23, 2014, 11:00 am Pacific / 2:00 pm Eastern
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Corrective and Preventive Action (CAPA) is one of the most challenging quality system elements that companies face during inspections and audits. CAPA is a fundamental management tool that should be used as such in every quality system by implementing better metrologies and applying effective risk-based filters. A robust and effective CAPA program is especially important for medical device manufacturers. An effective CAPA system that identifies and eliminates (potential) non-conformities enables both regulatory compliance and at the end cost savings. Join TÜV SÜD America for their webinar CAPA E-ssentials to learn more about the importance, requirements, and essential elements of a CAPA program. The webinar will also discuss common pitfalls and guidance on how to implement a CAPA system. Click here to register.

Making the Case for Tying Business Systems to Quality: Creating a Compliance Hub for Your Enterprise
Tuesday, July 29, 2014 11:00 am Pacific / 2:00 pm Eastern
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As businesses grow and expand, they often see an increase in complexity. This comes from a global market, rapid pace of business and consumer demand, and more and more business systems to keep up with the pace of business. Amidst this complexity, compliance and quality are at a premium--companies need to keep up with their demand, and maintain a high level of compliance. Many leading organizations are seeking ways to improve operations, while keeping compliance as the central "hub" for their business.

In this webinar you will learn more about how companies are building solutions to create a central hub for quality and compliance and the common processes and business systems that tie into this hub.

Kimberly-Clark will present how they were able to achieve an integrated system by linking their Quality Complaint Handling system to their Salesforce.com platform. See how this enabled them to increase visibility, response times, and connection from post-market events to quality and compliance processes.

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