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Israel Medical Device Market Country Report

The Israeli Ministry of Health's Department of Medical Devices (AMAR) is responsible for oversight of the country's medical device market. However, the Israeli medical device regulatory system is based on prior marketing authorization in and one of the five founding Global Harmonization Task Force countries: Australia, Canada, Europe, Japan or the United States.

Let Emergo assist you in evaluating the Israeli medical device regulatory framework as it applies to your device(s)

Leveraging our global network of consultants as well as industry and regulatory contacts, Emergo can provide in-depth analysis of multiple medical device markets, including Israel. The following topics are covered in our Global Regulatory Overview reporting service for the Israeli market:

  • Regulatory Background on AMAR and the Israeli Ministry of Health
  • Product Assessment
  • Authorized Representation Requirements in Israel
  • Medical Device Registration Requirements
  • Costs and Timeframes
  • Labeling and Language Requirements
  • Regulatory Roadmap for Israel

Please contact us for more information about our Regulatory Overview Report for Israel

Ask us for detailed information about Israel regulatory strategy services.

Learn about the process, costs and timelines.

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