Whitepaper documentation

Here you can find documentation files of our services and white paper of our company

Guide to the Software as a Medical Device (SaMD) Regulatory Requirements

By: Asaf Azulay, Rebecca Feldman, September 2020

Li-Med Brochure

Since 2007 Li-Med has been working with both domestic and international
customers to formulate and execute successful regulatory activities and quality assurance, exclusively serving the medical device industry

Feel free to contact us:

  • This field is for validation purposes and should be left unchanged.
Menu