MANCHESTER, England and DEERFIELD, N.H., July 21, 2016 /PRNewswire/ -- MAE Consulting
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With expertise in commercializing medical and in vitro diagnostic devices, MAE Consulting markets products globally and across the Atlantic -- in either direction.
The new MAE office in Manchester, England is strategically located to take full advantage of the UK government's Northern Powerhouse initiative supporting innovation and the MedTech community in northwest England.
UK advantages include its centrality to Europe and the USA, a growing economy, and a highly educated and technically skilled talent pool.
The American marketplace is challenging to companies seeking to bring products to market, and to export and import them, particularly in the tough regulatory environment surrounding medical and diagnostic devices.
"With MAE Consulting, there's no need to 'mind the gap.' Our specialists have expertise navigating the alphabet soup of regulatory acronyms, from FDA (Food and Drug Administration) to the BIS (Bureau of Industry and Security) and the EAR (Export Administration Regulations) to the ISO 13485 Certification necessary to deliver MedTech innovations to the global marketplace," said Janet Kwiatkowski, President of MAE Consulting Group LLC.
The world of import and export licensing and compliance is complex. Trade compliance and medical regulations vary from the USA to the EU and the UK. With MAE Consulting's presence in England, clients are ensured that their intellectual property, sensitive medical devices, and technical imports and exports reach the global marketplace in full regulatory compliance.
Kwiatkowski added, "The UK has a vibrant and growing global MedTech ecosystem. MAE's team of professional consultants is proud to offer signature specialist support to companies seeking to strategically market their innovative MedTech devices to the USA and the world."
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SOURCE MAE Consulting Group
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