The SOA certification is the compulsory certification for participation in tenders for the execution of public works contracts, i.e. a document necessary and sufficient to prove, during the tender, the company's ability to execute, directly or by subcontracting, public works with a base amount higher than € 150,000.00; it certifies and guarantees the possession by the company in the construction sector of all the requirements provided for by the current regulations on Public Works Contracts.
UNI EN ISO 9001:2015.
The standard specifies the requirements for a quality management system for an organization that: a) needs to demonstrate its ability to consistently deliver a product that meets customer and applicable mandatory requirements; b) wishes to enhance customer satisfaction through the effective application of the system, including processes to continuously improve the system and ensure compliance with customer and applicable mandatory requirements.
UNI EN ISO 13485:2012
The standard specifies requirements for quality management systems that enable an organization to demonstrate its ability to provide medical devices and related services that comply with customer requirements and regulatory requirements applicable to those medical devices.
Clearance to mark 93/42/EEC.
Enabling of 93/42/EEC marking (medical gas supply units - bedhead beams). The EEC Directive 93/42 on medical devices (abbreviated as MDD 93/42), published in the Official Journal of the European Union in June 1993, is a document that sets out the general criteria to be used in the design and manufacture of certain categories of medical devices, in force in the countries of the European Union. It imposes the obligation of CE marking for the marketing of these devices (MD); to obtain the CE marking, essential requirements must be met.
Certification 93/42/EEC (H@H).
Qualification for 93/42/EEC marking (H@H Device). The EEC Directive 93/42 on medical devices (abbreviated as MDD 93/42), published in the Official Journal of the European Union in June 1993, is a document that sets out the general criteria to be used in the design and manufacture of certain categories of medical devices, in force in the countries of the European Union. It imposes the obligation of CE marking for the marketing of these devices (MD); to obtain the CE marking, essential requirements must be met.
EN ISO 14001:2004.
The standard specifies the requirements for an environmental management system (EMS). It is the result of a company's voluntary choice to establish/implement/maintain/improve its own environmental management system. Being certified UNI EN ISO 14001:2004 demonstrates that the organization has a management system suitable to keep under control the environmental impacts of its activities, and systematically seeks to improve in a consistent, effective and above all sustainable way.
OHSAS 18001:2007 Certificate
In many industries, an efficient management system for risk prevention is essential. The system focuses on risk control factors, and an occupational health and safety management system, identifies and assesses the possibility of workplace accidents. OHSAS 18001:2007 is an Occupational Health and Safety Management (OH&S) standard designed to offer a response to this need; certification to this standard allows companies to implement responsible risk control and continuously increase workplace safety and health to protect staff from hazards.
DESIGN, REALIZATION AND MAINTENANCE OF REMOTE MANAGEMENT AND CONTROL NETWORKS OF GAS PLANTS
MEDICAL AND TECHNOLOGICAL SYSTEMS. PROVISION OF TELEMEDICINE SUPPLIES AND SERVICES AND RELATED MANAGEMENT ACTIVITIES. RESEARCH AND DEVELOPMENT ACTIVITIES IN THE TECHNOLOGICAL AND BIO-MEDICAL FIELD.
INSTALLATION OF GAS-MEDICAL SYSTEMS.INSTALLATION OF TECHNOLOGICAL SYSTEMS.RESEARCH AND DEVELOPMENT ACTIVITIES IN THE TECHNOLOGICAL AND MEDICAL FIELD.