EVENTS AND EXHIBITIONS
Join us for the following events to learn how our products and services will help you meet your go-to-market strategy for your IVD and medical devices in over 100+ global markets.
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.
We will host a webinar on advanced product registration techniques for faster global access several times over the coming weeks. 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.
Register for one of the webinars below.
Webinar: Advanced Product Registration Techniques for Faster Global Access, Webinar: Advanced Product Registration Techniques for Faster Global Access
April 26, 2017 at 10am PDT
Webinar: Advanced Product Registration Techniques for Faster Global Access,
May 3, 2017 at 3pm BST
May 10, 2017 at 10am PDT Webinar: Advanced Product Registration Techniques for Faster Global Access
May 17 , 2017 at 3pm BST
If you are not planning to attend any of the events or exhibitions listed above, you can request a personal demo with a member of our team online, any time.