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    Webinar on The 510(k) Submission: Requirements, Contents, and Options

    View: 246

    Website http://bit.ly/1iChWKZ | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: June 17, 2014 | Date: June 17, 2014

    Venue/Country: usa, U.S.A

    Updated: 2014-04-22 14:05:14 (GMT+9)

    Call For Papers - CFP

    Overview:

    This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly. Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory and financial health.

    Your goal is to get the 510(k) through the review process as quickly as possible. This presentation will also distinguish between the standard, special and abbreviated 510(k)s, and explain when each is appropriate. This course will describe the submission process and the contents required by the FDA for a successful submission. It will also provide an understanding of the common pitfalls, delays, and possible preventive measures. Also described will be the type of activities a company can pursue while waiting for submission clearance.

    Areas Covered in the Session:

    When to submit a 510(k) for a new or modified product

    Types of 510(k) submissions and when to use each

    What is the submission process

    What is contained in a 510(k) submission package

    How to know whether clinical data is required

    How is the submission package assembled

    User fees and 510(k) submissions

    How to interact with the FDA and the reviewer

    Who Will Benefit:

    This webinar will provide valuable assistance to all medical device companies that prepare 510(k) submissions. The employees who will benefit include:

    Executive Management

    Regulatory Management

    Professionals involved with premarket notification to the FDA

    R&D personnel involved in approving the design of medical devices

    Sales personnel involved in approving the marketing of medical devices

    Quick Contact:

    GlobalCompliancePanel

    USA Phone:800-447-9407

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/1iChWKZ


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.