Li-Med’s Training

Founded in 2007. Li-Med provides domestic and international regulation administration as well as quality assurance services. By implementing its expertise and understanding of QA & RA system requirements, Li-Med has been successful in assisting medical companies pass the FDA, CE, and other application processes.

CE Mark – IVDR

In Vitro Diagnostics and the IVDR HomePagesWhat are In Vitro Diagnostics?In Vitro Diagnostics (IVDs) are devices and accessories that perform tests on specimens derived from the human body such as…

Sterilization Validation

Sterilization Validation HomePagesEO sterilization validationMedical device sterilization validation is one of the most important elements of medical device Validation & Verification plan, since compromised state of sterility of medical device…

Clients

Li-Med’s Clients HomePagesWe at Li-Med understand the vital importance of getting a medical device product to market swiftly.  Our services are tailored to suit your business needs to provide you…

Become PRRC

Person Responsible for Regulatory Compliance (PRRC) HomePagesEnsure EU regulatory compliance through the Person Responsible for Regulatory Compliance (PRRC)The Person Responsible for Regulatory Compliance (PRRC) is a new requirement of the…

Medical Device

Medical Device HomePagesWhat is the definition of a medical device? Each regulatory body or regulation such as the FDA or the European Regulation (MDR) will have its own definition of…

Integrate QA & Development

Integrate QA & Development HomePagesWhy should Quality Assurance (QA) and development be integrated?The fierce and intense cut-throat market requires companies to release their products to the market as quickly as…

HIPAA

HIPAA HomePagesHIPAA complianceThe Health Insurance Portability and Accountability Act (HIPAA) was enacted in 1996 by the US government to protect personal healthcare data from leaking out of the healthcare and…

IEC 62304

 IEC 62304 HomePagesIEC 62304 complianceThe IEC 62304 is an international standard outlining product life cycle processes pertaining to the development of software used with medical devices. It was developed by…

Strategize Regulation

Strategize Regulation HomePagesWhy do I need a regulatory strategy?Speed to market is important to your return on investment (ROI), particularly when trying to introduce an innovative medical product. The quicker…

ISO 27001

ISO 27001 HomePagesWhat is ISO 27001?ISO/IEC 27001:2013 (or ISO 27001) is an international standard that provides a foundation for establishing an information security management system (ISMS) in organizations. Its goal…

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