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How to Achieve 510(k) Application Success for Device Software: Avoid Pitfalls that Could Delay Your Market Entry
With countless forms and steps necessary to get a medical device approved, many organizations become frustrated when a device is rejected from entering the market. And then, the whole approval process starts all over again.
Learn what you need to do to pass your 510(k) submission the first time and avoid costly delays that can wreak havoc on your business.
Regulatory affairs expert Cheryl Wagoner clears up any confusion you may have regarding your application for devices that contain software in How to Achieve 510(k) Application Success For Device Software: Avoid Pitfalls that Could Delay Your Market Entry webinar CD and transcript set.
Calling on her 20 years of experience, Cheryl takes you by the hand and walks you calmly, carefully and expertly through the steps you need to take to move your application forward as quickly as possible. You'll learn answers to key questions, such as:
Most importantly, you'll take home Cheryl's all-inclusive checklist of items you must include in your application … items that will help ensure the software section of your 510(k) is complete and reviewer friendly.
Put an end now to the frustration of spending endless hours filling out countless forms only to find that your submission has been rejected and you're back to square one.
Instead, turn to an acknowledged expert whose experience — and checklist —will take the guesswork out of your 510(k) application process.
Cheryl Wagoner has 20 years of experience in quality assurance and regulatory affairs. She currently is the Principal Consultant/Owner of Wagoner Consulting LLC, where she provides consulting services to medical device and pharmaceutical companies. Previously, she has held various positions in Quality, Regulatory, Clinical and Compliance in the medical device and pharmaceutical industries.
Cheryl is a member of Regulatory Affairs Professionals (RAPS), Association for the Advancement of Medical Instrumentation (AAMI), Medical Device Manufacturers (MDMA) FDA Working Group, and the MDMA Compliance Working Group. She completed the RAPS Executive Development Program at the Kellogg School of Management.
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