Quality Assurance

LIBYTEC PHARMACEUTICAL S.A. has developed a Quality Management System and it is implemented in the activities “Import, Trading of Pharmaceutical Products, Medical Devices and Cosmetics/ Supervision of the Production, Storage and Distribution of the above Products”.

The Quality System implemented by the Company has been developed taking into account the requirements of both ISO 9001:2015 and ISO 13485 Standards, Ministerial Decision of 2016 (National Identifier ΔΥ8δ/Γ.Π. οικ./1348, Governmental Gazette 32 16.01.2004): Principles and guidelines for good practice in the distribution of medicinal devices, as well as the applicable legislation and regulations governing the operation of the Company and the products that the Company trades.

The Quality Policy is linked with the Company’s philosophy and the market needs, as well as the requirements of both the clients and the applicable legislation.

The quality policy provides the framework for establishing quality objectives, includes a commitment to meeting the applicable requirements, and includes a commitment to continual improvement of the Quality Management System.

The primary goals of the Quality Management System include the observance of the obligations governing the Company’s relationship with clients, the compliance of the products distributed and the services provided with clients’ quality requirements, as well as the optimisation of the financial result.