The start UP
Labfit's commitment to quality was defined in the company's genesis and, in 2014, it was recognized for the first time, through the certification of the Quality Management System by the ISO 9001 standard. This certification was the company's initial objective, consolidating its requirement in work methodologies and their position in the national and international context.
The Triple Certification
With the implementation of an integrated management system in 2015, Labfit consolidated its organizational structure, guaranteeing the quality of the services provided and extending the scope of the System to Research and Development activities and the particular requirements of Medical Devices, assuming the commitment to comply with the requirements of the normative references: ISO 9001 (Total Quality Management), NP 4457: 2007 (Research, Development and Innovation Management) and ISO 13485: 2003 (Medical Device Quality Management System).
The GLP in 2016
In the strategic guidelines for the coming year, the recognition of INFARMED, according to the OECD Principles of Good Laboratory Practices, constitutes a decisive milestone for the company, allowing Labfit to present itself as a reference in supporting safety tests in cosmetic and pharmaceutical products.
Additionally, Labfit is recognized by the National Innovation Agency as a suitable entity for R&D, thus covering its clients by SIFIDE (SYSTEM OF TAX INCENTIVES TO BUSINESS R&D).
THE SYSTEMS OF QUALITY, HIGH RIGOUR AND DEGREE OF REQUIREMENT IMPLEMENTED AT LABFIT ARE ITS INSTRUMENT TO MAKE QUALITY THE ROUTINE AND TO MAKE ROUTINE THE OPPORTUNITY FOR CONTINUOUS IMPROVEMENT IN THE PROSECUTION OF EXCELLENCE.