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 a webinar.

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Webinar: Advanced Product Registration Techniques for Faster Global Access,
June 28, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
July 5, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
July 12, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
July 19, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
July 26, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
August 2, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
August 9, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
August 16, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
August 23, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
August 30, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
September 6, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
September 13, 2017 at 10am PDT

Webinar: Advanced Product Registration Techniques for Faster Global Access,
September 20, 2017 at 3pm BST

Webinar: Advanced Product Registration Techniques for Faster Global Access,
September 27, 2017 at 10am PDT

2017 RAPS Regulatory Convergence, National Harbor at the DC Waterfront,
September 9-12,2017 (book meeting with us below)


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.

REQUEST A PERSONAL DEMO>

latest news
  • Jun 27 2017
    2017 RAPS: DON’T MISS INVALUABLE INSIGHTS ON REGULATORY STRATEGIES FOR MARKET ACCESS

    MedTech regulatory affairs professionals managing the launch of products in new markets and maintaining market approval globally will benefit from the invaluable insights shared during the ‘Regulatory Strategies for Market Access’ session at this year’s R...

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  • Jun 13 2017
    FDA TO REQUIRE NEW VALIDATION DATA FOR LIST OF REUSABLE MEDICAL DEVICES

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  • Jun 11 2017
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  • Jun 7 2017
    FDA EXTENDS UDI COMPLIANCE DEADLINES FOR LOW-RISK MEDICAL DEVICES

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  • Jun 5 2017
    AUSTRALIA: CONSULTATION ON COMPARABLE OVERSEAS REGULATORS FOR MEDICAL DEVICES OPENS

    Australia’s Therapeutic Goods Administration (TGA) is seeking comments from the MedTech industry and regulators on the use of marketing approval by comparable overseas regulators for medical devices in overseas markets to support the inclusion of them in ...

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VANCOUVER OFFICE

  • Phone +1 604.681.6888
  • Fax +1 604.681.6822
  • info@arazygroup.com
  •  
  • #350-1333 Johnston Street
  • Pier 32, Granville Island
  • Vancouver, British Columbia
  • Canada V6H 3R9

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