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ISO 9001

ISO 9001 - Quality management systems

The quality management systems is a standard that focuses on process management of the company, meet the requirements of the customer, ensuring specified parameters, provision and management of suppliers so as to ensure that input will be of the required quality.

The term process management, respectively. processes can be understood in all the activities, which make up the functioning of the entire company (purchasing, management, document and records management, personnel management, metrology, manufacture, inspection and maintenance of machinery, occupational health and safety management, etc.).

When we say that the process we make with a controlled manner means that we eliminate the chance of potential errors and shortcomings in these processes. The idea of standards is therefore in process control in such a way that results are in the maximum customer satisfaction.

The standard is very compatible and variable, so it is possible to implement it (introduce) for any type of organization (production, service provision, commerce, etc.). In production is most important to know traceability of the product itself, from initial customer requirements through the purchase of goods from a supplier, receiving goods from a supplier, placing, removal, entering into production, the actual movement of goods / product after manufacture, inspection required parameters of the product, packing and preparing for shipping, delivery to the customer, billing and after its screening of satisfaction.

EN ISO 14001

The requirements of this standard covers the complete management system of the organization in order preventive action on the impacts to the environment, and at the same time minimizing the impact of existing products and the organization's environment. Among other things, the standard is directed at fulfilling the legislative requirements and their regular assessment of compliance, which is mainly provided to help prevent from fines or sanctions from public authorities.

The standard is very compatible and variable, so it is possible to implement it (introduce) for any type of organization (production, service provision, commerce, etc.), It is important to properly identify and manage environmental aspects of the organization.

OHSAS 18001

Requests are routed to allow the organization to manage risks associated with occupational health and safety, and improve their own performance. Funds contributed to the implementation and certification of an effective safety management system leads to reducing the incidence of occupational diseases and industrial accidents, to minimize the costs associated with workplace accidents and reduce the likelihood of penalties for violation of legislation on health and safety at work.
The standard is very compatible and variable, so it is possible to implement it (introduce) for any type of organization (production, service provision, commerce, etc.). Fulfillment of legal requirements applies to any legal person.

ISO/IEC 27001

Information security management system according to ISO 27001 is documented system proving that the identified assets are protected, information security risks are managed, measures are in place with the required level of assurance and controlled. The aim is to reduce risks arising from the analysis of the organization, and have in place measures to ensure that risks are tolerated far managed and controlled. For assets are considered not information occurring within the organization (customer, technology, financial flows organizations on product / service organization, etc.), But also a physical tangible assets affecting the security of the organization as such (eg. Key mode organizations , security and protection of the organization's use of allocated objects organization (PC, mobile), and so on.).
The standard is very compatible and variable, so it is possible to implement it (introduce) for any type of organization (production, service provision, commerce, design and development of software, etc.). Norma takes equally into account the requirements of stakeholders, external and internal contexts and demands of customers, owners, suppliers that need to be incorporated into the internal control system.

ISO/TS 16949

Production site is defined as a workplace where manufacturing takes place with value-added processes. Production is defined as the process of creating production materials, parts or assemblies, heat treatment, painting or finishing.

The aim is to provide the overall improvement of the organization, what were previously difficult to manage will be monitored and controlled with "transparent" manner and with a "stable quality „ and organization discipline. Furthermore, important aspects of quality management is to focus on the specific requirements of automotive customers and the commitment of top management of the organization at all levels. The specificity of this standard is that it is necessary to specify customer requirements for quality in terms of product, process and system.

The technical requirements of ISO / TS 16949 is designed for organizations providing mass production of spare parts in the automotive industry, of any material.

ISO 50001

The intention is to enable an organization to follow a systematic approach to achieving continual improvement of energy efficiency, energy efficiency, energy use and consumption in the organization. ISO 50001 can be implemented in the organization itself, or even integrated, for example. with ISO 9001 or ISO 14001 is intended for all types of organizations that wish to have a set energy policy and the public be proved by a certificate. ISO 50001 is based on the model of management system of continuous improvement, where one of the monitoring parameters is also continuous improvement of energy management, resulting in financial savings.

EN ISO 11137

ISO 22000

ISO 22000 integrates the principles of the Hazard Analysis and Critical Control Point (HACCP) and steps to implement it developed the Codex Alimentarius Commission. ISO 22000 at the same time takes into account the requirements of ISO 9001 so that both standards are mutually compatible. ISO 22000 can be applied within the organization itself or as part of an integrated quality management system.
Certification to ISO 22000 brings a comprehensive, dynamic and efficient risk monitoring the hygiene of foodstuffs, based on hazard analysis and good manufacturing practice and enhancement of food safety throughout the chain store business.

ISO 13485

As it is a sector largely treated worldwide law, is a fundamental objective of ISO 13485 harmonize the legal requirements of the quality management systems of medical devices. ISO 13485 is a standard which is based on ISO 9001, but includes some particular requirements for medical devices such as: risk analysis, sterile manufacturing and Traceability. Standard omits some of the requirements of ISO 9001 that are not necessary as legal requirements. Because of these gaps can not be an organization certified to ISO 13485 compliance with ISO 9001.

Continuity of legal requirements for approval of medical devices.
For manufacturers of medical devices is a fundamental legal approach to product market. National regulations often refer to the ISO 13485 and require it as part of the approval process for medical devices, such as the EU Directive on medical devices (Directive on medical devices 93/42 / EEC, Directive diagnostic agents in vitro 98/79 / EC, Active implantable medical devices 90/385 / EEC). The company DNV is also appointed by the notified bodies on the implementation of the conformity assessment under Annex II, IV and V of the Directive medical devices 93/42 / EEC. Manufacturers certified according to ISO 13485: 2003 fulfill the requirements for a quality management system in all classes of this Directive.

EN ISO/IEC 17025

This International Standard specifies the general requirements for the competence to carry out tests and / or calibrations, including sampling. It covers testing and calibration performed by standard methods, non-standardized methods, and laboratory-developed methods.

ISO 16363

ISO IATF 16949

ISO / TS 16949, a quality management system for the automotive industry, was first developed in 1999 in cooperation with the International Automotive Task Force (IATF) and ISO / TC 176 Technical Quality Standards (ISO). Since then, it has become one of the most used international standards in the automotive industry, which aims to harmonize the diverse assessment of certification systems in the global automotive supply chain.

IATF announced that it will publish a new International Standard IATF 16949: 2016 in October 2016, replacing the current ISO / TS 16949: 2009. The new IATF 16949: 2016 will be in line with the latest version of ISO 9001: 2015 and will fully respect its structure and requirements . This standard will not be a separate quality management standard, but will be introduced as a complement to ISO 9001: 2015.

IATF works closely with the ISO organization through its participation in ISO / TC 176. This ensures compliance with ISO 9001.

It is important to note that IATF 16949: 2016 will fully respect the ISO 9001: 2015 structure and for this reason the same time is set for both standards - 3 years, which was launched by issuing the ISO 9001 standard in September 2015 and ending in September 2018.

ISO 3834

Concerning the increased demands for quality and safety of these products it is important to ensure that welding processes were carried out efficiently using all appropriate instruments of control. From the perspective of customers and stakeholders, it is a significant part of management system, as non-compliance of the requirements of the welding process can have far-reaching effects on health, wealth and ecology.

Your benefits at a glance

to exercise its products in areas where filling ISO 3834 in production becomes an essential condition for the selection
procedures (eg the area of pressure equipment, building steel constructions, etc.).
gaining a tool to support the fulfillment of the requirements of standards and regulations that apply to welded structures
increase business competitiveness
increase the credibility and reliability to customers

EN ISO 10006

EN ISO 10006

ISO 22716

ISO/IEC 20000-1

This part of ISO / IEC 20000 is a service management system (SMS) standard. Defines the requirements for the service provider to plan, set up, implement, operate, monitor, assess and improve SMS. Requirements include the design, transition, delivery and improvement of services to meet service requirements. Figure 2 shows the SMS, including service management processes. Different service providers may implement service management processes and process relationships in different ways. The type of relationship between the service provider and the customer affects how the service management processes are implemented.

ISO/IEC 27018

This document establishes commonly accepted control objectives, controls and guidelines for implementing measures to protect Personally Identifiable Information (PII) in line with the privacy principles in ISO/IEC 29100 for the public cloud computing environment. In particular, this document specifies guidelines based on ISO/IEC 27002, taking into consideration the regulatory requirements for the protection of PII which can be applicable within the context of the information security risk environment(s) of a provider of public cloud services.

ISO 37001

This document specifies the requirements and provides guidance for establishing, implementing, maintaining, reviewing and improving the anti-corruption management system. The system can be stand-alone or integrated into the overall management system. In connection with the organization's activities, this document focuses on the following areas: corruption in the public, private and non-profit sectors; for corruption committed by the organization; for corruption by the staff of the organization acting on behalf of or for the benefit of the organization; for corruption by the organisation's partners acting on behalf of or for the benefit of the organization; to corrupt the organization's personnel in relation to the organisation's activities; to corrupt the material partners of the organization in relation to the activities of the organization; for direct and indirect corruption (for example, for a bribe offered or received through a third party or a third party). This document only covers corruption.

ISO 45001

This document specifies the requirements for an occupational safety and health management system (OSH) and provides guidance on their use to enable organizations to provide safe and healthy workplaces with the prevention of accidents at work and health deterioration, as well as proactively improving its OSH performance. This document is applicable to any organization that wants to create, implement and maintain a health and safety management system to improve occupational safety and health, eliminate hazards and minimize health and safety risks (including system deficiencies), take advantage of health and safety management opportunities and manage health and safety management system mismatches. which are connected with its activities. This document helps the organization achieve the intended results of its OSH management system. In accordance with the organization's OSH policy, the intended results of the OSH management system include: continuous improvement of OSH performance; compliance with legal and other requirements; achieving health and safety objectives.

ISO 14021:2016

Environmental labels and declarations — Self-declared environmental claims (Type II environmental labelling)

PMES Technologies s.r.o.

PMES Technologies s.r.o.

AS Engineering

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IRISA, výrobní družstvo

EU POLYMER CZ, odštěpný závod

VH-FB EURO, s.r.o

Grupa Azoty Polyolefins S.A.

Plast-invest EU, s. r. o.

KONTINENT PLAST s.r.o.