No label defined (Q3542887)

From EU Knowledge Graph
Revision as of 23:12, 17 November 2021 by DG Regio (talk | contribs) (‎Created claim: summary (P836): High standards (Good Manufacturing Practice-GMP) and extensive legal requirements must be met in order to ensure the protection of patients and other users when manufacturing products for medical technology that can affect people’s health and quality of life in the broadest sense. Therefore, extensive training is necessary for the employees, who work in the cleanroom areas and monitor the production. These trainings include validation, qu...)
Jump to navigation Jump to search
Project Q3542887 in Germany
Language Label Description Also known as
English
No label defined
Project Q3542887 in Germany

    Statements

    0 references
    2,207.74 Euro
    0 references
    2,759.68 Euro
    0 references
    80.0 percent
    0 references
    7 May 2018
    0 references
    30 September 2018
    0 references
    Röchling Medical Neuhaus GmbH & Co. KG
    0 references
    0 references

    50°29'44.02"N, 11°7'4.48"E
    0 references
    98724 Neuhausam Rennweg
    0 references
    Bei der Herstellung von Produkten für die Medizintechnik, die im weitesten Sinn die Gesundheit und Lebensqualität von Menschen beeinflussen können, sind hohe Standards (Good Manufacturing Practice-GMP) und umfangreiche gesetzliche Vorgaben einzuhalten, um den Schutz der Patienten und anderen Anwender zu gewährleisten. Deshalb sind umfangreiche Schulungen für die Mitarbeiter notwendig, die in den Reinraumbereichen arbeiten und die Produktion überwachen. Diese Schulungen beinhalten u.a. die Validierung, Qualifizierung und Verifizierung der Bereiche und Produkte. Die hier geplante Maßnahme umfasst 4 Schulungstage. Der gewählte B-DKS wurde gewählt, weil er den Anforderungen am ehesten entspricht. (German)
    0 references
    High standards (Good Manufacturing Practice-GMP) and extensive legal requirements must be met in order to ensure the protection of patients and other users when manufacturing products for medical technology that can affect people’s health and quality of life in the broadest sense. Therefore, extensive training is necessary for the employees, who work in the cleanroom areas and monitor the production. These trainings include validation, qualification and verification of the areas and products. The action planned here covers 4 training days. The selected B-DCS was chosen because it is most likely to meet the requirements. (English)
    18 November 2021
    0 references

    Identifiers

    DE_TEMPORARY_ESF_138799
    0 references