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  • International product registrations - Where do I begin?

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Wednesday - Jul 17, 2013 10:00 AM
  • End Time:
  • Wednesday - Jul 17, 2013 11:00 AM
  • Location:
  • Online
  • This webinar on international product registrations will discuss how to develop a plan, implement medical device and pharmaceutical registrations in a timely, efficient manner to help reduce your company's time to market. Best practices in document legalization will be covered too.

    Why Should You Attend:

    International product registration has changed with the advent of new regulations across the globe. Requirements have changed, more documentation is needed in some cases. In Hague convention member states and non-Hague member states, companies can lose revenue simply by not having the right legalized documents.

    The process for approval or clearance of devices outside the USA varies from regulatory body to regulatory body. In some cases, products achieve regulatory approval in an efficient and timely manner. In others, including the US FDA, companies may face a protracted and delayed approval process. Furthermore, recent scrutiny by US regulators and legal authorities is making it more uncertain for companies attempting to gain market access in foreign countries.

    This training will provide a guide to facilitate international registrations and reduce time to market by two months. Learning the relevant regulatory requirements and the appropriate document legalization path will speed up the pathway.

    Learning Objectives:

    Participants in this class will learn how to develop a plan, implement product registrations in a timely, efficient manner to help reduce their companies time to market.
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