510(k) Updates: Trends, New Strategy and FDA Clearance



This webinar will provide an opportunity to get familiar with an FDA’s process to communicate with the industry early in the process for sustainable 510(k) preparation and submission including recent 510(k) trends and updates.

This webinar is intended to discuss how to put together a pre-submission (Q-submission) to obtain FDA feedback on your proposed questions, which will be helpful and useful for your device design, preclinical and clinical study plan and design, if applicable.

Based on speaker’s recent experience, he will discuss contents and format for a Q-submission, 510(k) preparation and submission compliant with the FDA’s eCopy and RTA policy, helping you streamline your dialogue with the FDA for maximum benefits while preparing for a successful 510(k) in a least burdensome, efficient and effective manner.

In this webinar, the speaker will share his PASS-IT solutions based on what he has learned from his own experience including his recent analysis of various different types of 510(k)s that have been recently cleared.

This webinar is a must for regulatory professionals working in medical device industry including those who are interested in the topic.

Areas to be Covered:

Statute(s) And Regulations
Device Classification
Identifying Predicates: Key Factors
510(k) Program
When a 510(k) Is Required
Applicable Regulatory Requirements: Biocompatibility, Software, Risk Management, etc.
Pre-Submission (Q-Submission) for a 510(k): Requirements, Contents and Format
Substantial Equivalence: Factors to Consider and Special Considerations
Addressing e-Copy And RTA Policy Requirements
Common Mistakes for RTA Policy Requirements
Applicable Standards and Guidance
510(k) Contents And Format
Common Pitfalls and How to Prevent Them
What to Ensure While Preparing Your Q-Submission and a 510(k) Application
Responding to FDA’s Request of Additional Information.
Resolving Different Opinions and Interpretations
Best Practices for a Q-submission
Best Practices for a 510(k) Preparation, Submission and Clearance
Speaker’s Practical, Actionable and Sustainable Solutions (PASS)

Who will Benefit:

Regulatory Affairs Teams
Research & Development Teams
Contractors / Subcontractors
Senior Management
Anyone interested in 510(k) matters

Dr. David Lim, Ph.D., RAC, ASQ-CQA. Dr. Lim is President and Principal of Regulatory Doctor (www.RegulatoryDoctor.us). As a leading industry speaker, Dr. Lim frequently presents global regulatory and quality compliance topics 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 eight 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 pharmacovigilance, medical device reporting, recalls and patient safety signals being conducted at the Regulatory Doctor. Dr. Lim currently serves as a member of the Advisory Board for Inspection Insider published by FDA News.


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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance