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Whether you are developing a new product, improving an existing product, require assistance with the EU or FDA, or are simply trying to comply with the myriad of regulation and standards, Li-Med’s services will accelerate your company’s success and profitability.

Since 2007, we have been working with different medical device companies them quality assurance and regulatory consulting as well as process outsourcing.

You should speak to us if you would like to:

Build from scratch or streamline your quality system

Have a clear regulatory strategy that will bring your device to market following the shortest possible route

Be helped with regulatory submissions

Ready your company for an upcoming audit, such as ISO, FDA, CE-marking, Canadian Medical Devices Conformity Assessment System (CMDCAS), UL’s electrical medical device certification , or else

We work with you every step of the way and tailor solutions and scale our services to meet your specific needs

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