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Jeff Kasoff

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• DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them -...

  By GlobalCompliancePane on March 26, 2012 - To be in substantial compliance with FDA and ISO regulations, there are many documents that must be maintained by your firm. ... [+]

  Read more
  DHF       dhr       DMR       FDA and ISO regulations       Jeff Kasoff       Regulatory Documents Explaine       Seminar Pennsylvani

• Live webinar on The 510(k) Submission: Requirements, Contents, and Options

  By Compliance2go on January 19, 2012 - 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 dev Read more
  510       510 k       fda       Jeff Kasoff

Jeff Kasoff

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