Introduction: Learn about the International Railway Industry Standard (IRSI) according to ISO/TS 22163 in order to understand and implement the specific requirements for Obsolescence Management, Reliability-Availability-Maintainability (RAM), Life Cycle Considerations (LCC) and Initial Type Inspection (FAI) as well as the general requirements of these standards. Trainer competence: Several years of experience in the railway industry and in the implementation of ISO/TS 22163 distinguish our trainers for this seminar. Objective: Participants understand the specific requirements of ISO/TS 22163 and are able to implement them in their company. Content: o   Railway industry and quality management o   legal and official framework conditions o   Customer requirements, risk and project management o   Audit planning and execution according to ISO 19011:2018 o   Normative requirements of ISO/TS 22163:2017 and ISO 9001:2015 (IRIS - International Railway Industry Standard) o   Certification process according to ISO/TS 22163:2017 Requirements: none Target group: Persons from the railway and supplier industry who are to introduce a QM system or carry out internal audits in accordance with ISO/ TS 2216 Duration: 2 days Literature: Seminar documents Price per participant open training:               1.100,00 EUR Price per company internal event:                 6.600,00 EUR  

Introduction: Learn about the International Railway Industry Standard (IRSI) according to ISO/TS 22163 in order to understand and implement the specific requirements for Obsolescence Management, Reliability-Availability-Maintainability (RAM), Life Cycle Considerations (LCC) and Initial Type Inspection (FAI) as well as the general requirements of these standards. Trainer competence: Several years of experience in the railway industry and in the implementation of ISO/TS 22163 distinguish our trainers for this seminar. Objective: Participants understand the specific requirements of ISO/TS 22163 and are able to implement them in their company. Content: o   Railway industry and quality management o   legal and official framework conditions o   Customer requirements, risk and project management o   Audit planning and execution according to ISO 19011:2018 o   Normative requirements of ISO/TS 22163:2017 and ISO 9001:2015 (IRIS - International Railway Industry Standard) o   Certification process according to ISO/TS 22163:2017 Requirements: none Target group: Persons from the railway and supplier industry who are to introduce a QM system or carry out internal audits in accordance with ISO/ TS 2216 Duration: 2 days Literature: Seminar documents   The price includes the seminar documents, lunch and coffee breaks during the 2-day seminar.

Introduction: Learn about the International Railway Industry Standard (IRSI) according to ISO/TS 22163 in order to understand and implement the specific requirements for Obsolescence Management, Reliability-Availability-Maintainability (RAM), Life Cycle Considerations (LCC) and Initial Type Inspection (FAI) as well as the general requirements of these standards. Trainer competence: Several years of experience in the railway industry and in the implementation of ISO/TS 22163 distinguish our trainers for this seminar. Objective: Participants understand the specific requirements of ISO/TS 22163 and are able to implement them in their company. Content: o   Railway industry and quality management o   legal and official framework conditions o   Customer requirements, risk and project management o   Audit planning and execution according to ISO 19011:2018 o   Normative requirements of ISO/TS 22163:2017 and ISO 9001:2015 (IRIS - International Railway Industry Standard) o   Certification process according to ISO/TS 22163:2017 Requirements: none Target group: Persons from the railway and supplier industry who are to introduce a QM system or carry out internal audits in accordance with ISO/ TS 2216 Duration: 2 days Literature: Seminar documents   The price do not include travel cost such as hotel, flight etc. for the trainer. The cost for training rooms and catering during the inhouse event will be carried by the client.

SAP ADDON MIC/3:DIRECT CONNECTION OF MEASUREMENT EQUIPMENT TO SAP QMThe measurement equipment interface connector MIC/3 is a cost-effective add-on for direct online measurement value recording via the SAP interface and transaction. MIC/3 allows direct connection of measurement equipment via diff erent interface systems to the SAP QM application and is also incorporated directly into SAP results recording.MIC/3 supports all common interface systems for interface boxes, e.g. Steinwald, Bobe, Mitutoyo, Ibrit, Elias, Brecht, etc.. Alternatively, measurement equipment can be connected directly to the PC easily via the COM/USB interface – in this case, no interface box is required.A free demo version is available.

Introduction: The purpose of quality management is to create trust for the customer in the performance of a company. This trust is of particular importance when medical products are involved and consumers rely on the effectiveness of the medical products. Acquire competence in the implementation of quality management for medical devices and comprehensive knowledge of the requirements of the standard DIN EN ISO 13485:2016. Through clear practical examples and exercises, you will learn about the special focuses, legal and regulatory requirements and advantages that this standard offers your company. Trainer competence: Several years of experience in the production of medical devices and projects for the implementation of DIN EN ISO 13485 in companies distinguish our trainers for this seminar. Goal: Participants understand the specific requirements of DIN EN ISO 13485:2016 and are able to implement them successfully in their company. Content: o   Sense, purpose and advantages of quality management for medical devices -       Requirements of interested parties o   Identification of legal and regulatory framework conditions -       European directives and medical devices law -       Risk management according to DIN EN ISO 14971 ·   Requirements for risk management and market monitoring ·   Required documented information -       Placing medical devices on the market -       Medical Device Safety Plan Ordinance o   Requirements and implementation of a quality management for medical devices according to DIN EN ISO 13485:2016 and DIN EN ISO 9001:2015 o   Conformity assessment and declaration o   Duties, rights and cooperation with consultants and security officers o   Market monitoring and reporting system o   Control of the processes by means of key figures o   Organization of audit activities in the quality management system for medical devices o   Evaluation of the effectiveness of the quality management system o   Competence check or final examination Requirements: none Target group: Persons and managers who are involved in the production of medical devices and who want to introduce and implement a quality management system. Duration: 5 days Literature: Seminar documents and relevant legal texts Price per participant open training:               2.600,00 EUR Price per company internal event:                 16.500,00 EUR

Introduction: The purpose of quality management is to create trust for the customer in the performance of a company. This trust is of particular importance when medical products are involved and consumers rely on the effectiveness of the medical products. Acquire competence in the implementation of quality management for medical devices and comprehensive knowledge of the requirements of the standard DIN EN ISO 13485:2016. Through clear practical examples and exercises, you will learn about the special focuses, legal and regulatory requirements and advantages that this standard offers your company. Trainer competence: Several years of experience in the production of medical devices and projects for the implementation of DIN EN ISO 13485 in companies distinguish our trainers for this seminar. Goal: Participants understand the specific requirements of DIN EN ISO 13485:2016 and are able to implement them successfully in their company. Content: o   Sense, purpose and advantages of quality management for medical devices -       Requirements of interested parties o   Identification of legal and regulatory framework conditions -       European directives and medical devices law -       Risk management according to DIN EN ISO 14971 ·   Requirements for risk management and market monitoring ·   Required documented information -       Placing medical devices on the market -       Medical Device Safety Plan Ordinance o   Requirements and implementation of a quality management for medical devices according to DIN EN ISO 13485:2016 and DIN EN ISO 9001:2015 o   Conformity assessment and declaration o   Duties, rights and cooperation with consultants and security officers o   Market monitoring and reporting system o   Control of the processes by means of key figures o   Organization of audit activities in the quality management system for medical devices o   Evaluation of the effectiveness of the quality management system o   Competence check or final examination Requirements: none Target group: Persons and managers who are involved in the production of medical devices and who want to introduce and implement a quality management system. Duration: 5 days Literature: Seminar documents and relevant legal texts   The price does not include travel cost such as hotel, flight etc. for the trainer. The cost for rooms and catering during the inhouse event will be carried by the client.

Introduction: The environment in which we all live is shaped not least by industrial companies and is becoming increasingly important in our society. Acquire competence in the implementation of environmental management and comprehensive knowledge of the requirements of the DIN EN ISO 14001:2015 standard. Through clear practical examples and exercises, you will become familiar with the special focuses, legal and official requirements and advantages that this standard offers your company. Trainer competence: Several years of experience in industry and projects for the implementation of DIN EN ISO 14001 in companies distinguish our trainers for this seminar. Goal: Participants understand the specific requirements of DIN EN ISO 14001:2015 and are able to implement them successfully in their company. Content: o   Sense, purpose and advantages of an environmental management system -       Requirements of interested parties o   Identification of legal and regulatory framework conditions -       Structure of environmental law -       Waste/cycle management, water law, emission control -       Law on hazardous substances and chemicals -       Environmental liability and criminal consequences o   Requirements and implementation of an environmental management system according to DIN EN ISO 14001 o   Communication on the project for the introduction and maintenance of the environmental management system o   Planning of emergency preparedness and hazard prevention o   Evaluation of relevant environmental topics on the basis of key figures o   Organization of audit activities in the environmental management system o   Evaluation of the effectiveness of the environmental management system o   Competence Check      Requirements: none Target group: Persons from environmental management and executives who want to introduce an environmental management system or integrate it into the existing quality management. Duration: 4 days Literature: Seminar documents and relevant legal texts Price per participant open training:               1.800,00 EUR Price per company internal event:                 11.500,00 EUR

Introduction: The environment in which we all live is shaped not least by industrial companies and is becoming increasingly important in our society. Acquire competence in the implementation of environmental management and comprehensive knowledge of the requirements of the DIN EN ISO 14001:2015 standard. Through clear practical examples and exercises, you will become familiar with the special focuses, legal and official requirements and advantages that this standard offers your company. Trainer competence: Several years of experience in industry and projects for the implementation of DIN EN ISO 14001 in companies distinguish our trainers for this seminar. Goal: Participants understand the specific requirements of DIN EN ISO 14001:2015 and are able to implement them successfully in their company. Content: o   Sense, purpose and advantages of an environmental management system -       Requirements of interested parties o   Identification of legal and regulatory framework conditions -       Structure of environmental law -       Waste/cycle management, water law, emission control -       Law on hazardous substances and chemicals -       Environmental liability and criminal consequences o   Requirements and implementation of an environmental management system according to DIN EN ISO 14001 o   Communication on the project for the introduction and maintenance of the environmental management system o   Planning of emergency preparedness and hazard prevention o   Evaluation of relevant environmental topics on the basis of key figures o   Organization of audit activities in the environmental management system o   Evaluation of the effectiveness of the environmental management system o   Competence Check      Requirements: none Target group: Persons from environmental management and executives who want to introduce an environmental management system or integrate it into the existing quality management. Duration: 4 days Literature: Seminar documents and relevant legal texts   The price includes the seminar documents, lunch and coffee breaks during the 4-day seminar.

Introduction: The environment in which we all live is shaped not least by industrial companies and is becoming increasingly important in our society. Acquire competence in the implementation of environmental management and comprehensive knowledge of the requirements of the DIN EN ISO 14001:2015 standard. Through clear practical examples and exercises, you will become familiar with the special focuses, legal and official requirements and advantages that this standard offers your company. Trainer competence: Several years of experience in industry and projects for the implementation of DIN EN ISO 14001 in companies distinguish our trainers for this seminar. Goal: Participants understand the specific requirements of DIN EN ISO 14001:2015 and are able to implement them successfully in their company. Content: o   Sense, purpose and advantages of an environmental management system -       Requirements of interested parties o   Identification of legal and regulatory framework conditions -       Structure of environmental law -       Waste/cycle management, water law, emission control -       Law on hazardous substances and chemicals -       Environmental liability and criminal consequences o   Requirements and implementation of an environmental management system according to DIN EN ISO 14001 o   Communication on the project for the introduction and maintenance of the environmental management system o   Planning of emergency preparedness and hazard prevention o   Evaluation of relevant environmental topics on the basis of key figures o   Organization of audit activities in the environmental management system o   Evaluation of the effectiveness of the environmental management system o   Competence Check      Requirements: none Target group: Persons from environmental management and executives who want to introduce an environmental management system or integrate it into the existing quality management. Duration: 4 days Literature: Seminar documents and relevant legal texts   The price does not include travel cost such as hotel, flight etc. for the trainer. The cost for rooms and catering during the inhouse event will be carried by the client.

Introduction: Sustainable action, including the use of energy, is becoming increasingly important in our society. Acquire competence in implementing energy management and comprehensive knowledge of the requirements of this standard. Particular focal points of this standard on energy efficiency are clearly explained. Trainer competence: Several years of experience in the energy industry and projects for the implementation of DIN EN ISO 50001 in companies distinguish our trainers for this seminar. Aim: Participants understand the specific requirements of DIN EN ISO 50001 and are able to implement them successfully in their company. Content: o   Legal and political background to energy management -       Renewable Energy Sources Act (EEG) -       Renewable Energies Heat Act (EEWärmeG) -       Energy Saving Act (EnEG) -       Energy Saving Ordinance (EnEV) o   Recording energy data and consumers o   Development of key figures for the evaluation of energy consumption and calculation of profitability o   Possible improvement approaches to reduce energy consumption o   Possibilities for energy recycling o   Development of an energy program taking into account the changes in the processes of the company and the behavior of the employees o   Purchasing strategies for energy procurement o   Audit of the energy management o   Applying for subsidies o   Competence Check      Requirements: none Target group: Persons from quality or energy cost management and executives who want to introduce an energy management system or integrate it into the existing quality management. Duration: 3 days Literature: Seminar documents Price per participant open training:               1.550,00 EUR Price per company internal event:                 9.500,00 EUR