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Service Provider - Labelling device

Service Provider
  1. GREGOR. PRZEDSIĘBIORSTWO WIELOBRANŻOWE

    Poland

    The company GREGOR. PRZEDSIĘBIORSTWO WIELOBRANŻOWE, is a Multi-Category, which operates in the Cash registers, automatic industry. It also operates in the Cash registers, Cash registers, Cash registers for the retail trade, price label units, and Hand labelling devices industries. It is based in Włocławek, Poland.

  2. PACKAGING SERVICE CENTER

    Belgium

  3. 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

  4. THERMAL PRINTER SERVICES

    United Kingdom

    At Thermal Printer Services we specialism in the supply of new and reconditioned thermal printers, including Zebra Printers, Data max Printers and other top brand thermal label printers at competitive prices. We also offer a full range of support services for thermal label printers, bar code label printers, ID card printers, handheld bar code scanners and EPOS equipment, repairs and maintenance contracts to suit your requirements. Our best selling printer consumables include printer labels: thermal transfer labels and direct thermal labels, printer ribbons and thermal printheads, for our range of Thermal Printers, ID Card Printers & EPOS Equipment.We also offer a range of in-house and on-site repair and maintenance services to suit your individual business requirements including thermal printer repairs, handheld device and EPOS equipment repairs.

  5. SYNCHRONICA PLC

    United Kingdom

    Synchronica plc is a leading developer of next-generation mobile messaging solutions. Mobile Gateway, Synchronica's flagship product, provides push email, synchronization, instant messaging (IM), and social networking services to any mobile phone currently in use. Synchronica's patented transcoding engine uses advanced streaming to download email attachments and can dramatically reduce the consumption of network bandwidth by as much as 90 percent. Mobile operators and device manufacturers from emerging and developed markets rely on Synchronica's white-labelled product for providing mass market messaging services across the entire customer base, diversifying revenues and reducing churn. Headquartered in England, Synchronica also maintains a development center in Germany and the Philippines in addition to a regional presence in Canada, the USA, Hong Kong, Spain, and Dubai.

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  1. MEDIQUASAR CONSULENZA

    Italy

    With the experiences I acquired the following skills: to make/prepare the Clinical Evaluation Based On The Literature, to extension of an existing clinical evaluation ; to resolve the issues concerning the regulatory aspects of: classification of the specific type of the product, CE, marketing authorizations, import / export permits, verify the accuracy of labeling, compliance with the requirements of 'U.S. FDA 510 (k) Medical Device Submissions Requirements, preparation of the technical documentation for medical devices, etc.; to know the requirements on Clinical Investigations; to know the ISO 14155: 2012; to translate.