Overcoming Regulatory Hurdles for Devices

7 Dec 2017 12:30pm

The Entrepreneurs’ Programme Learning Event brings together two experts in the field that will be able to assist SMEs to understand from a regulatory and operational perspective what is required to ensure ISO13485 compliance.

This workshop will be valuable to both companies that have this accreditation but also those making transitions and aspire to operate in the medical device sector.

 

Andrew Batty
Andrew is an experienced MedTech CEO that has developed, executed and managed business strategies to commercialise innovative and emerging technologies. Andrew has secured ISO13485 certification for manufactured devices and recruited distributors for overseas markets.

Seamus Orr
NSW Manager for PharmOut, a rapidly growing international consultancy offering GMP compliance, qualification and validation, TGA regulatory, engineering and architectural consulting services.

 

Date:  Thursday, 7 December 2017
Time:  12.30pm 0 4.00pm
Where:  Deloitte Office Melbourne, 550 Bourke Street, Melbourne

 

For more information on this event, please contact Julie-Anne White on 0412 357 891.

 

 

 

 

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Deloitte Office Melbourne