Live event: Wednesday, February 1 at noon New York time

Today, registering products is subject to local language requirements and commercial bylaws. You need to appoint a local authorized representative and few manufacturers have the resources, knowhow, or expertise required to obtain marketing licenses beyond a few major markets.

Looking for help, the industry resorts to distributors or remote third party consultants. This is bad because the license is then owned by the distributor who controls the market – not you.

In this presentation, you’ll learn about a readily available cloud-based solution to:
• Expedite product clearances;
• Process multiple registrations in multiple countries on one platform on a fixed budget;
• Keep ownership of your product; and,
• Allow in-market sales and marketing activities sooner.

The content is timely because many regulatory agencies around the world established or are implementing public health policies concerning medical device pre-market approvals. Manufacturers are placing more effort to enter new markets and industry growth relies on global markets rather than solely the traditional US, EU, and Japanese markets.

Benny Arazy will present the live webinar on Wednesday, February 1 at noon New York time. Register even if you can’t make the live event because we will record the broadcast and share the slides with all who register.

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