Quality and Compliance

We know that precision and quality are the decisive criteria for our customers, and we offer them the best and most reliable solutions for their needs

Global QM System

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All locations around the world use a quality management system to EN ISO 13485 or EN ISO 9001. LAP processes are globally harmonized and certified, to ensure efficient collaboration and smooth processes between our locations.

As a medical product manufacturer certified to EN ISO 13485, we meet the industry's rigorous standards. In medical products, quality is essential, as it directly impacts patients' safety and well-being. We regularly and successfully undergo audits by our customers.

Our processes are constantly being refined and optimized to achieve further improvement in our performance.

Product Approvals and Registrations

  • Our products have all the necessary approvals and registrations almost everywhere in the world (including CE, FDA, SFDA, CFDA/NMPA).
  • Product testing is done by an independent, world-leading organization to internationally recognized standards.
  • Advantage for LAP customers: our products meet local regulatory requirements and can be imported without complications.

Manuals

  • Manuals per EN 82079 are provided for each product. From installation to use to service call, all phases are described clearly and practically.
  • We can provide manuals in any required national language (ISO 17100). Users can thus quickly learn how to operate the products efficiently and safely.

Compliance

  • Our Code of Conduct documents the principles and values we adhere to in all interactions with our employees, customers, suppliers, society, and the environment as we engage in daily business.
  • We are conscious of our responsibility to use conflict-free materials in our products. The use of these resources is specified in our Sourcing Guideline with respect to conflict materials.

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