EVENT IS OVER

US FDA MedicalDevice 510(k)Submission-510(k)for aChange to anExistingDevice

Tuesday, Apr 11, 2017 at 10:00AM - 1:00PM
Fremont, CA

Event Details

Description
This webinar ensures your company gets a broader perspective of how and what to do to get a quick and non-debatable or questionable approval for your 510K product. All are different so this presentation will not just be specific for a specified Medical Device that is currently being marketed and your company wants the same opportunity to produce and sell that product.

Objectives Of The presentation
Medical device technology is constantly evolving, and the approval for another company to produce the same approved Medical Device product requires FDA's review and consent. The new FDA 510K recommendations are intended to provide guiding principles to help manufacturers determine when an intended product or minor change to a legally marketed medical device subject to premarket notification in compliance with the 510K requirements is significant enough to warrant FDA review and approval, including major changes or modifications to the intended use that could significantly impact safety and effectiveness (patient risk).
  • Whenever a manufacturer changes its device, it must take certain actions to comply with the QS regulation, 21 CFR Part 820, unless a regulatory exemption exists. The QS regulation which includes your CAPA procedure requires that design changes and production and process changes be documented and proven to be just as good and not generating any patient risk and notifying the FDA for this change from the original approval prior to implementation.
  • In evaluating whether a change requires a new 510(k), manufacturers have to consider whether there are any unintended consequences, needed clinical trials or effects of the device change. For example, changes in sterilization may unintentionally affect device materials, or changes to materials may unintentionally affect the performance of the device.
  • FDA Briefing Documents - The purpose of the pre-facility meeting is to provide detail and seek FDA's input regarding your company’s proposed new manufacturing facility or the new manufacturing process, single use disposable manufacturing technology and to confirm that the proposed approach will provide adequate comparability data between the product that was proven to be functional based on the clinical results and now as is going to be used for commercial manufacturing in the new facility since the product produced in the pilot facility and used for the initial Phase II/III clinical trials.
Why Should you Attend
Generate the technical comprehension and technical writing capabilities to eliminate corporate interpretations and translations of technical terms relative to the specifics of your specific process needed for a 510K submission. We always want to make the submission in a way that does not require any interpretation and delay. In order to get a quick approval the FDA should read the documents & come to the same conclusion that we did to generate the production process for this product ensuring we are not generating any patient risk.

Who will Benefit
  • Regulatory Affairs Managers, Directors and VPs
  • Clinical Affairs Managers, Directors and VPs
  • Quality Managers, Directors and VPs
  • Compliance Managers and Directors
  • Complaint Handling and Risk Management Managers and Directors
  • Site Managers, Directors, and Consultants
  • Legal Counsel
  • Quality Assurance
  • Product Development
  • Executive Management, such as CEO, Owner, President, Vice President
  • Regulatory specialists who compose 510(k) applications for software
  • Manufacturers of medical devices
  • Project managers and documentation specialists
  • Medical writers
For Registration
http://onlinecompliancepanel.com/webinar/US-FDA-MEDICAL-DEVICE-510k-508586/APRIL-2017-ES-EZEVENT

Note: Use Promo code DE5YU and get 10% off on registration (Valid till APRIL 30th 2017)

Organization Details

Online Compliance Panel (OCP) creates and delivers comprehensive industry relevant training sessions. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Live interactions on compliance training make the process holistic and effective. OCP largely emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices and market trends.

We strive to incorporate high standards in developing a culture facilitating exchange of ideas resulting in functional excellence. OCP believes in nurturing ideas and thought processes through innovative e-learning methodologies. Our products and services are designed to offer customized solutions to industry and market. We bridge the gap between experience and knowledge thus delivering original and creative content.

Our objectives of employing interactive mediums ensure effective communication and mutual exchange of ideas. OCP closely follows best practices and regulatory trends in the global compliance scenario. We also observe and communicate trends witnessed in FDA, ISO regulations, process and design validation. All updates and additions to important laws can be accessed by our customers in real time.

Our mission is to empower compliance professionals through effective online training sessions. Our world class training methodologies stem from comprehensive understanding of client requirements. The content conforming to FDA and ISO standards is developed by well qualified and experienced industry leaders. Our offerings will exceed expectations and add value to your investment.

The content in various categories such as medical devices, pharmaceuticals and biotechnology will raise the bar in terms of quality already on offer .We hope to contribute to the creation of responsible organizations creating benchmarks in quality, integrity and transparency.

Online Event
38780 Tyson Lane, Apt 210
Fremont, CA 94536

Starts April 11, 2017 at 10:00AM - 1:00PM

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Contact Information

Organization: Online Compliance Panel LLC

Event Contact: OCP Panel

Phone: 15108575896