This seminar is scheduled upon request.
- Scheduling for LIVE webinar can be made by email to firstname.lastname@example.org or email@example.com
- Duration: 60 Minutes
About the Seminar
This presentation will walk you through how to prepare and submit a traditional premarket notification [510(k)] for clearance from US FDA. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices (IVDs) in the US.
The section [510(k)] of the Federal Food, Drug, and Cosmetic Act (FD&C Act or the Act) describes statutory requirements for 510(k)s. The 510(k) premarket submission is made to US FDA to demonstrate that the subject device (to be marketed) is substantially equivalent (as least as safe and effective) to a legally marketed device (predicate device). In other words, a 510(k) must demonstrate that a proposed product is substantially equivalent to another, legally marketed medical device that is also lower-risk and is not subject to premarket approval (PMA).
Over the years, the 510(k) program has significantly evolved, affecting the 510(k) decision-making process. On July 28, 2014, FDA issued the finalized 510(k) guidance integrating a total of 400 comments received in response to the Draft Guidance issued on December 28, 2011. To expedite the process of bringing a product to market through the 510(k) program, it is imperative the medical device makers understand the recent changes, prepare and submit a quality 510(k) in a way to expedite the review process for fast and successful clearance.
In this 60-min presentation, the speaker will guide you through the details of the required elements in your 510(k) submission for successful clearance. You will have opportunities to bring great value and benefit to your firm’s 510(k) preparation, submission and clearance in an efficient and effective manner.
About the Areas to Be Discussed
- Applicable statute(s), regulations, and definitions
- Device classification
- FDA’s finalized 510(k) guidance, issued on July 28, 2014
- Who is subject to a 510(k)
- What actions require a 510(k) including three types of 510(k)s
- How to identify a predicate(s)
- 510(k) preparation compliant with eCopy and RTA policy (recent RTA items cited by FDA)
- 510(k) content and format
- Writing a cover letter: importance
- What to include and address in 510(k) submissions
- FDA de novo process – current good practices
- How to present scientific, technical, and/or clinical data
- How to demonstrate substantial equivalence (SE)
- How to increase 510(k) submission quality
- How to respond to FDA’s request of additional information
- How to resolve different opinions between the submitter and FDA reviewer(s)
- Speaker’s PASS-IT suggestions/recommendations
About the Benefits to Attend
- Gain and receive great guidance on 510(k) preparation, submission and clearance
- Get updated with the latest information and tips
- Learn the critical areas and common mistakes
- Improve your current practice
- Recognize what is important
- Become better aware of and get familiar with the 510(k) process
- Much more
About the Intended Attendee(s)
- Regulatory Affairs
- Clinical Affairs
- Legal Counsel
- Compliance Officers
- Senior Management
- Anyone interested in the topic.
About the Seminar Speaker
Dr. Lim is President and Principal of Regulatory Doctor. Dr. Lim frequently presents global regulatory and quality compliance topics including 510(k)s in various forums and meetings. Recently, Dr. Lim developed 510(k) templates ready for use compliant with e-Copy and RTA policy. In addition, Dr. Lim developed FDA inspection checklists for drug and medical device manufacturers based on his analysis of FDA inspectional observations cited in 483s for the past seven years. Dr. Lim provides his feedback to regulatory agency (e.g., US FDA) through public comments and also served as a panel member during the FDA’s transparency public meeting in 2009. Dr. Lim contributes to the Regulatory Affairs Professional Society (RAPS) as an author and speaker. Dr. Lim leads and directs all research projects including, but not limited to, pharmacovigilance, medical device reporting, recalls and patient safety signals being conducted at the Regulatory Doctor. Dr. Lim serves as a member of the Advisory Board for Inspection Insider published by FDA News.
Options to Request a LIVE 510(k) LIVE Online Seminar
- Option 1: you may send your “request to purchase” by email to Global Compliance Seminar
- Option 2: you may request an invoice by email to Global Compliance Seminar
- Option 3: you may purchase below using a credit card or PayPal below.
LIVE (one attendee): $199
LIVE (≤ 5 attendees): $599
LIVE (≥ 6 attendees): $999
LIVE & Recorded: $299
Last Updated: 2015-12-30