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Applications for production planning - Service Provider - Germany

GermanyService Provider
  1. TH DATA GMBH

    Germany

    The company TH DATA GMBH, is a Service Provider, which operates in the Software for industry industry. It also operates in the production planning, and applications for production planning industries. It is based in Berlin, Germany.

  2. SCHOTT SOFTWARE SOLUTIONS

    Germany

    The company SCHOTT SOFTWARE SOLUTIONS, is a Service Provider, which operates in the Software creation and development industry. It also operates in the applications for production planning industries. It is based in Ebersdorf B. Coburg, Germany.

  3. HORGES GMBH LAGERTECHNIK

    Germany

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    We are a manufacturer that supplies high-quality steel shelving at low prices. We have been operating as a manufacturer of high-quality shelving systems for over 25 years. We provide quality-tested steel shelving, storage shelves, compartment shelves and filing shelves for warehouses, workshops and archiving. Our shelving is available galvanised or with plastic coating. We develop solutions for clients in industry, commerce, trade and archiving. We design both bolted and boltless shelving to your specific requirements and usually dispatch it within 48 hours. We can provide you with special shelving solutions for storing almost any kind of material. We are also happy to plan your entire storage area. Our product range includes: Archive shelving, storage shelves, special shelving for a variety of applications, heavy-duty shelving systems, shelving systems and stainless steel laboratory shelving.

  4. 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