As you work to achieve your goal for compliance and regulatory operational readiness, it can be challenging to ensure you are meeting the necessary regulations and standards. In this session we will look at each category of the operational readiness model to break out the compliance elements for each category to help guide your readiness plan and priorities.
- Harry Benson, CAI Director of Human Performance
- Cheryl Bondurant, CAI Principal Consultant
Free to attend. Advance registration required HERE. After registering, look for confirmation email.
Cheryl is a professional with 41 years of experience working in FDA and ISO regulated environments. She has implemented effective compliant quality systems for medical devices, biologics, in-vitro diagnostics and electronics.
Cheryl is an instructor of FDA regulations and ISO standards and implementation for Quality Systems for Medical Devices and Current Good Manufacturing Practices for Finished Pharmaceuticals.
A former nuclear-trained submarine officer and Master Training Specialist, he is an expert in organizational effectiveness, performance improvement, human error reduction, and learning design and delivery with over 25 years of experience in driving results-based performance improvements within a variety of highly technical environments.