QUALITY POLICY

DK Diagnostics™ has as Quality Policy the FOCUS ON THE CUSTOMER

DK Diagnostics™, manufacturer of in vitro diagnostic products, has its Quality Management System in accordance with market requirements, continuous improvement of customer-focused processes, fully based on compliance with ISO 13485 and RDC 16 requirements. ANVISA. It also complies with the requirements of Directive 98/97/EC on medical devices and in vitro diagnostics.

Rigorous controls are applied since the selection of our suppliers and throughout the production chain in order to guarantee and ensure the quality of all our products.

PLEASE REQUEST OUR CERTIFICATES

SCIENTIFIC ADVISORY SERVICES
DK offers different and complete support to technicians and users regarding any doubts or technical-scientific details that may arise.

CERTIFICATION
QUALITY MANAGEMENT SYSTEM
CERTIFICATE ISO 13485