Name: Latest FDA Proposed Changes to the Process and Bullet Proof 510(k) Seminar
Start: 2016-09-22T09:00:00-04:00
End: 2016-09-23T18:00:00-04:00
Location: Courtyard Seattle Sea-Tac Area

Course "Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:
This Two-day course is a primer and overview to the premarket notification process, i.e., a 510(k). 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.

For more than 30 years, the 510(k) process has consistently done a good job of protecting patients against unsafe products. The process is well designed to assess the safety and effectiveness of low and moderate risk medical devices whose risks are well understood from experience with similar devices. Various industry trade groups and associations are now somewhat concerned that the number and scope of FDA's recently proposed 510(k) changes could negatively impact the agency's mission to ensure American patients have timely access to safe and effective medical technologies.

In comments submitted to FDA in response to the agency's release in August 2010 of more than 60 proposals to change the 510(k) process, industry has advocated that instead of implementing an extensive list of potentially disruptive proposals, FDA should focus on the proposals the agency has advanced that enjoy broad agreement and consensus, such as: increased reviewer training, development of specific and relevant guidance documents, and enhancements or improvements to the de novo review pathway, among other suggestions. This 1-day primer and course will provide an update to these proposals as appropriate and where we stand but more importantly, provide direction, guidance and clarity on preparing for, executing and submitting your 510(k) application.

Who will benefit:

CEOs &CFOs in medical device companies
VPs, Directors and Heads of Regulatory Affairs
VPs, Directors and Heads of Clinical Affairs
Senior and line Marketing and Sales Management
Regulatory Consultants
Risk Managers
Engineering & R&D
Professionals involved with premarket notification to the FDA
R&D personnel involved in approving the design of medical devices
Medical device sales and marketing personnel
Production & Operations

Objectives:

This seminar will provide an overview and in-depth snapshot of the process for preparing for and managing an FDA inspection efficiently, effectively and successfully. You will learn and understand how FDA trains its investigators and inspectors so that you can prepare and always be in a state of readiness. Attendees who will benefit include all levels of management and departmental representatives from key functional areas and those who desire a better understanding or a "refresh" overview of the FDA inspectional process, strategy, the tools to be used to assess and gauge state of preparation and readiness, including:

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

Agenda: Day 1 Schedule

Lecture 1: 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.

Lecture 2: 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

Day 2 Schedule

Lecture 3: Interactive Q&A, Wrap-Up and Adjourn

Q&A with all participants and 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 and participants should be prepared to address any issues and challenges as experienced on behalf of their company in this open-forum and interactive session

Speaker: David R. Dills

Regulatory Affairs & Compliance Consultant,

David R. Dills, Global Regulatory Affairs & Compliance Consultant, has an accomplished record with more than 26 years of experience within regulatory affairs, compliance and quality consultative services for early-stage/established Class I/II/III medical devices, IVDs, and bio/pharmaceutical manufacturers on the global landscape. Previously employed, with increasing responsibilities by device manufacturers and consultancies, including a globally recognized CRO, has worked directly with and for manufacturers engaged in compliance remediation activities involving consent decrees, CIA's, FDA warning letters, and customer generated compliance events, provides Strategic GxP Compliance and Regulatory Consulting, handles all aspects of global regulatory submissions and dossiers, including 510(k), PMA, Design Dossiers, Technical Files, CMC, NDA, and IDE submissions, currently serves as a U.S. Agent, works with stakeholders and Center Reviewers regarding submission meetings/negotiations, clinical affairs, and provides regulatory submissions and post-market project leadership/guidance covering different therapeutic and medical specialties based on classification. His background encompasses broad capabilities in regulatory and compliance oversight and governance, including CAPA, Design Controls, Validation, Software Quality with regulatory oversight, FDA Mock Inspections, remediating documentation management systems, Supplier Quality, Adverse Event Reporting, Product Complaints, GxP Training, interpretation and applicability of FDA and international regulations and standards, postmarketing surveillance, ISO 13485 and CE Mark, Medical Device/IVD/Active Implantable Directives. Mr. Dills leads and manages efforts involving multi-country product registrations and licensing in Asia Pacific, EMEA and The Americas from premarketing to postmarketing, and works with the Regulatory Authorities and strives to provide consistent, practical compliance solutions that work with reduction of regulatory compliance risk.

Location: Seattle, Washington Date: September 22nd & 23rd, 2016 and Time: 09:00 AM to 06:00 PM

Venue: Courtyard Seattle Sea-Tac Area

Address: 16038 West Valley Highway Tukwila Washington 98188 USA

Price: Register now and save $200. (Early Bird)

Price: $1,295.00 - Without Stay

Until August 10, Early Bird Price: $1,295.00 from August 11 to September 20, Regular Price: $1,495.00

Price: $1,695.00 - With Stay

Until August 10, Early Bird Price: $1,695.00 from August 11 to September 20, Regular Price: $1,895.00

Until August 10, Early Bird Price: $8,475.00 from August 11 to September 20, Regular Price: $8,675.00

Quick Contact: NetZealous DBA GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884