2012 - Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel

Overview: A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA.
There are three types of Premarket Notification 510(k)s that may be submitted to FDA: Traditional, Special, and Abbreviated. The Special and Abbreviated 510(k) methods were developed under the "New 510(k) Paradigm" to help streamline the 510(k) review process. Product modifications that could significantly affect safety and effectiveness are subject to 510(k) submission requirements under 21 CFR 807 as well as design control requirements under the Quality System (QS) regulation. Under the QS regulation, all Class II and III devices and certain Class I devices are required to be designed in conformance to 21 CFR 820.30 Design Controls. FDA provides guidance and this course will address key resources when making critical decisions.
Objectives:
Know the differences between the Traditional, Special and Abbreviated submissions
Understand Substantial Equivalence and how it is applied
Who is required to submit the application to FDA
Where to submit the 510(k) and what to expect with the review and approval process
When it is and is not required if you are a device company
Exemptions to the submission process and special considerations
How to locate a "predicate" device and go through the content and format of the 510(k)
Understand the De Novo process and the expectations for possibly marketing a low risk device
Understand the potential impact of FDA's proposed changes to the 510(k) process and why manufacturers need to pay attention
Detailed Agenda:
Introduction and Regulatory Background
There is no 510(k) form; however, 21 CFR 807 Subpart E describes requirements for a 510(k) submission.
Current trends with the 510(k) process.
The Process
Who is Required to Submit a 510(k)
When a 510(k) is Not Required
When a 510(k) is Required
Locating and justifying the Predicate
Substantial Equivalence and demonstration of SE to another legally U.S. marketed device
How to Prepare Submissions
510(k) Submission Methods
List of forms associated with Premarket Notification 510(k) submissions
Deciding When to Submit a 510(k) for a Change to an Existing Device
What happens if FDA requires additional information and data and your responsibilities
Interactive Q&A, Wrap-Up and Adjourn
Q&A with all attendees
Group discussion and review of recent 510(k) clearances and proposals and recommendations between FDA and industry
Discussion Points: some of the recommendations have included, but not limited to, redefining fundamental terms, limiting use of predicates, greater authority to rescind 510(k)s, etc.
510(k) Frequently Asked Questions
Attendees should be prepared to address any issues and challenges as experienced on behalf of their company in this open-forum and interactive session
Who will benefit: This course is appropriate to those involved in all aspects of the premarket notification, i.e., 510(k) process on behalf of medical device and In Vitro Diagnostic manufacturers. It is both a primer for personnel new to the FDA 510(k) process, or an excellent refresher course for those who need to revisit the basics and fundamentals for a better understanding on how to prepare and submit your application to ensure regulatory and compliance success.
Those who will benefit includs:
R&D
Quality Assurance
Quality Control
Production
Operations
Engineering
Compliance and Regulatory Affairs
All Levels of Management, including technical and laboratory personnel who desire to understand what it takes to prepare and submit a bulletproof 510(k) to FDA while at the same time are aware of the changing regulatory landscape regarding FDA's proposed changes to the 510(k) process.
Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
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