Vitro S.A has a management system that integrates quality and environment, R&D&I and information security certified and/or accredited in accordance with various prestigious international regulations and whose certificates can be downloaded on this page.
Aware of the importance of guaranteeing the security of the information we manage for our clients, especially all information related to health data, we have reinforced our commitment to guarantee CID (confidentiality, integrity and availability) for all our activities. To achieve this, we have implemented and certified an information security management system under the ISO 27001 standard.
With the aim of meeting all requirements and achieving the satisfaction of our customers and interested parties, guaranteeing environmental protection, we are certified under ISO 9001 and 14001 standards. In compliance with both standards Vitro, S.A. informs its suppliers that their evaluation is carried out based on an indicator based on the detection of incidents regarding the requirements and specifications that we establish for the products and/or services requested, as well as to comply with the requirements of the environmental management system. of the organization.
Likewise, our commitment to manufacturing and offering products of the highest quality and guarantee has led us to implement a quality management system certified under the ISO 13485 standard that ensures compliance with the legal requirements applicable to our medical products. At an international level, Vitro has also obtained recognition of its good manufacturing practices by health authorities, achieving the GMP certification issued by ANVISA.
The Clinical Diagnostic Laboratory of Master Diagnostics has obtained accreditation by the National Accreditation Entity ENAC, complying with the requirements established by the ISO 15189 Clinical Laboratories standard. Particular Requirements for Quality and Competence, for carrying out the studies whose scope is defined in its technical annex.
Our environmental management system has the objective of making the development of our business compatible with the preservation and respect for the Environment. We identify and measure the environmental aspects of our activity to understand and minimize the impact they have on the Environment. It is Vitro S.A’s commitment to communicate information related to its environmental performance, the achievement of its objectives and the improvement of results of its environmental indicators.
Additionally, as part of its commitment to improving environmental performance, Vitro has identified all the direct sources of Greenhouse Gases (GHG) over which it has control and has estimated the calculation of the organization’s carbon footprint, based on to the GHG Protocol standard. The report has been verified, with a limited level of assurance, by European Quality Assurance Spain, S.L. (EQA), accredited as a Report Verifier of the European Greenhouse Gas Emissions Trading Scheme (EN ISO 14065:2013, Implementing Regulation (EU) 2018/2067 as amended by Implementing Regulation (EU) 2020/2084 and EA-6/03), with no. 1/VV028 (previously no. 6/VCDE010).
The company’s R&D&I Vision and Strategy is available to all interested parties who request it. You can download our certificates and the Policy on which our management system is based here.
The policy is available to any interested party who requests it.
Over 30 years of experience in developing and manufacturing reagents for immunohistochemistry, molecular diagnostic products, instruments and software.
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