• europages
  • >
  • COMPANIES - SUPPLIERS - SERVICE PROVIDERS
  • >
  • reports

Results for

Reports

GermanyStuttgart, Freiburg and Baden-Wurtemberg
  1. DÜRR NDT GMBH & CO. KG

    Germany

    Verified by europages badge

    DÜRR NDT offers comprehensive digitisation solutions for the nondestructive testing (NDT) industry: Networked, digital radiography systems combined with innovative software. These include high-resolution image plate scanners (CR) and flat panel detectors (DDAs), software for image capture and analysis, standards-compliant digital archiving tools and the integrated NDT workflow management and reporting platform DRIVE NDT. The innovative systems from DÜRR NDT are always at the cutting edge of technology and continue to set new standards in terms of resolution, user-friendliness and durability. We are still the only CR manufacturer with a BAM-certified 30 μm basic local resolution worldwide! In almost 20 years, DÜRR NDT's X-ray inspection systems have established themselves in a variety of industrial applications, both mobile and stationary, and are used in more than 80 countries.

    All the products for "reports"
  2. ESCOMAG GMBH

    Germany

    Verified by europages badge

    ESCOMAG GmbH – consulting, services, seminars and process support for quality management, environmental management, risk management, quality assurance, quality control, management systems. We offer practice-oriented management consulting, system support, interim managers for the development or further development of your management systems for all common standards, for the automotive industry, medical technology, aerospace and the defence industry as well as in mechanical engineering. We are specialists in quality and environmental management with a focus on the implementation of integrated management systems, organisational development, support in quality assurance, screening inspections and reworking as well as in the training and coaching of employees. We support you with qualified employees and certification auditors. Our services in detail: – System audits (IATF 16949, DIN EN ISO 9001, DIN EN ISO 14001), process audits according to VDA 6.3 as well as CQI-Rules (CQI-9, CQI-12, CQI-14, CQI-23) and supplier audits. – Help with complaint management (automotive core tools 8D problem solving), complaint management, 8D systematics, Ishikawa, 5 Whys, problem analysis, problem solving method, root cause analysis, warranty processing, damaged parts analysis field, 8D report evaluation. – FMEA error possibilities and impact analysis. – Quality inspections, screening inspections, reworking. – Documentation, forms, certification preparation. – Training

  3. MECHASYS GMBH

    Germany

    mechaSYS GmbH is your DEVELOPMENT PARTNER in prototypes, samples and small series in sheet metal as well as electrical sheet metal. Prototype construction and small series production are the clear focus. Thus, we are not in competition with our customers, who usually produce themselves and can thus concentrate on their series processes/manufacturing as well as tool production. After all, nothing is more unsuitable for a toolmaker and/or plant manufacturer than when a customer has placed an order and then needs another 500 or 5000 prototypes before series production. Most of the time, it does not really fit into the production or the capacities are already planned with increasingly shorter delivery times. Possible consequence: Delayed deadlines or additional expenses. Our field of activity is to support you here. Contact Larkis of Dob Against this background, our entrepreneurial goal is: To grow together with our customers in the long term. www.mechaSYS.de

    All the products for "reports"
  4. COGNEX CORPORATION

    Germany

  5. MAXCERT LTD

    Germany

    Maxcert can provide the strategic and technical guidance to develop an appropriate project plan, as well as assist with the implementation of any stage of the MDR certification process. QMS / Risk Management - Strategy for Regulatory Compliance - MDR-Specific QMS Changes - Classification & Conformity Assessment - Other EU MDR Directives & Regulations - Risk Management Evaluation Criteria - Benefit Risk Analysis - MDR Readiness Audits Clinical Evidence - Guidance on New Clinical Evidence Requirements - Legacy Product Data Review - Performance Evaluation Plan / Report (PEP/PER) - Analytical Performance Report - Clinical Performance Plan / Report - Clinical Performance Study Plan (CPSP) - Scientific Validity Report Labelling & UDI - Intended Purpose / Claim Review - Labels & Instructions for Use Requirements - Applicable Standards - UDI Requirements & Symbols Technical Documentation - Technical Documentation Review & Preparation - GSPR Gap Assessments & Traceability Matrices - Test, Hardware, Software Requirements Post-Market Surveillance / Vigilance - Post-Market Surveillance Plan / Report - Post-Market Follow-up (PMPF) Plan / Report - Incident Reporting - Periodic Safety Update Report (PSUR) Economic Operators / EUDAMED - Person Responsible for Regulatory Compliance (PRRC) - Registration of EO’s & Devices - Control of Suppliers (Process/Method) To speak to an MDR expert, or if you don’t see the services you are looking for, contact us