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