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Thinking Regulatory? Think Li-Med! 


Whether you are developing a new product, improving an existing product, need assistance with the EU, 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.

Li-Med helps medical device companies navigate the challenging and ever-changing regulatory maze -- achieving product approvals and ensuring that quality systems pass even the most rigorous inspection.

We have worked with numerous Israeli medical device companies, offering them quality and regulatory consulting as well as process outsourcing.


You should speak to us if:

  •       You would like to build and manage your quality system more effectively.
  •       You would like a clear regulatory strategy that will bring your device to market by the shortest possible route.
  •      You need help with Technical Files (TF) and submissions to Notified Bodies (NB) and prefer to do it with outsourced resources.
  •      You want to be as ready as possible for an upcoming external udit (for ISO, CE, CMDCAS, UL or FDA).

 See the comprehensive list of services that we offer medical devices companies including biocompatibility testing through our partnership with Eurofins.


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