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Document preparation

3 Companies

32 Products

ESCOMAG GMBH

Germany

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

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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

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MDR Technical Documentation

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GERBU BIOTECHNIK GMBH

Germany

GERBU Biotechnik GmbH is an established company working in the biotechnology sector since 1986. We specialise in high-quality products for microbiology, cell research and analysis worldwide. Our experienced team offers a customised service and a wide range of products. We have been guaranteeing reliability, safety and unbeatable value for money for over 30 years. We are constantly expanding our portfolio through continuous improvement and co-operation with renowned partners. We are also committed to social responsibility and protecting the environment. You can rely on our careful product selection, transparent quality and fair prices for your research and development projects.

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ExoIsolator Exosome Isolation Kit

11-AMINO-1-UNDECANETHIOL Hydrochloride

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3 Companies