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Most creative developers and entrepreneual companies in the medical device industry have spend most their energi on the innovative processes and end up with a device and/or application ready for use - but still long under its way to market approval - because essential requirements and regulatory terms have not been addressed along the creative path.

 

How is your situation - are you well prepared - or do you need assistance initially finding out how you deal with regulatory affairs and market approval ??

 

Contact us to find out more about our full range of services.

 

info@mhealth-consult.dk

mHealth-Consult

mHealth Medical devices - stand alone mobile app or in combination with hardware

 

A revolutionary technology changing Global Welfare and Health Care

 

Prepare your mobile application, software and medical device for Global Sales

 

Planning

of

Market Approval

Development Focus

to

Assuring Appropriate

Quality and Safety

Regulatory Affairs

and

Market Approval

mHealth-Consult

Helping you on your way from Idea til Market

 

Focus on Safety, Quality and meeting Regulatory Requirements

Faster way to bring your products on Market

 

 

mHealth-Consult

Denmark

info@mhealth-consult.dk

mHealth-Consult

Bring your product faster to market - Assisting medical device developers with documentation and regulatory requirements

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