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CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA

ComplianceOnline

Thursday, October 19, 2017 at 8:30 AM - Friday, October 20, 2017 at 1:00 PM (PDT)

CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to...

Ticket Information

Ticket Type Remaining Sales End Price Fee Quantity
Seminar One Registration (Early bird price)
For Registrations till September 5, 2017 - $1699
40 Tickets Ended $1,699.00 $70.92
Seminar One Registration 40 Tickets Oct 19, 2017 $1,799.00 $73.92
Seminar One Registration (With 2 Nights Stay) 40 Tickets Oct 19, 2017 $2,249.00 $87.42

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Event Details

CLIA Waiver applications declined significantly after FDA’s CLIA Waiver guidance was published on January 30, 2008. Between 2008 and 2012, FDA reviewed 34 applications for CLIA Waiver and approved 14, sometimes taking years to issue a denial. The cost of performing CLIA Waiver studies, combined with the lengthy review times and likelihood of failure, discouraged companies from bringing new innovations to this critical public health sector.

As a result of MDUFA III, passed by Congress in 2012, FDA began accepting and reviewing Dual 510(k) and CLIA Waiver by Applications, and more companies are taking advantage of this new Dual Pathway, which promises shorter review time and higher success rates. Additionally, the 21st Century Cures Act Directs FDA to revise the section on Accuracy in the CLIA Waiver Guidance by the end of 2017. How will these changes impact CLIA Waiver Application outcomes?

You will leave this one and one-half day workshop knowing how to submit either a CLIA Waiver Application or a Dual 510(k) Waiver Application that conforms to FDA’s CLIA Waiver guidance. You will learn how to design risk-based “flex” studies, and develop cost-saving product development and clinical study strategies. We will review FDA’s CLIA categorization criteria and examine ways to incorporate “simple” and “negligible chance of erroneous results” into product design. You will understand how CLIA Waiver requirements have evolved, how the FDA determines performance requirements for CLIA Waiver, what to expect during their review and how to maximize your chances for a successful CLIA Waiver application. Finally, you will gain insights on what to expect from the anticipated new, revised CLIA Waiver guidance.

Learning Objectives:

Upon completing this course participants should be confident in their ability to:

  • Understand and follow FDA’s 2008 CLIA Waiver Guidance
  • Prepare an effective Pre-Submission for a CLIA Waiver of Dual 510(k) Waiver
  • Use the CLIA test complexity scoring criteria
  • Integrate human factors into device design
  • Design and execute “Flex” studies based on risk analysis
  • Design and execute CLIA Waiver or Dual Path clinical studies
  • Design and execute studies to evaluate performance at clinical decision points
  • Perform and present statistical analysis of data, including ATE and LER
  • Develop compliant labeling for CLIA Waived products
  • Prepare a CLIA Waiver or a Dual 510(k) Waiver Application
  • Avoid costly mistakes
  • Maximize the chances for a successful CLIA Waiver application

Who will Benefit:

This course is designed for people who are planning to undertake CLIA Waived product development, and people who will be involved in the supporting studies and submission of applications for CLIA Waiver to FDA. The course will address all levels of interest, from executive to technical and clerical. Personnel who will benefit from attending this course include:

  • Executives and Senior managers
  • R&D
  • Design engineers
  • Regulatory professionals
  • Project managers
  • Risk management professionals
  • Clinical research professionals


 For Registrationhttp://www.complianceonline.com/how-to-get-a-clia-waiver-for-medical-device-seminar-training-80217SEM-prdsm?channel=eventbrite

 

Note: Use coupon code < REFERRAL10 > and get 10% off on registration.

Have questions about CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA? Contact ComplianceOnline

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When & Where


San Francisco

San Francisco, CA

Thursday, October 19, 2017 at 8:30 AM - Friday, October 20, 2017 at 1:00 PM (PDT)


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Organizer

ComplianceOnline

At ComplianceOnline, we are focused on:

Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.

Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.

Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA
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