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    Attaining Your CE Mark for Your Medical Device in the EU

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    Website https://www.complianceonline.com/ce-mark-medical-device-webinar-training-706543-prdw?channel=Ourgloc | Want to Edit it Edit Freely

    Category

    Deadline: November 08, 2020 | Date: November 18, 2020

    Venue/Country: U.S.A

    Updated: 2020-10-05 15:46:53 (GMT+9)

    Call For Papers - CFP

    The letters ‘CE’ appear on many products that are traded on the single market in the European Economic Area (EEA). By placing the CE mark on a product, a manufacturer is declaring, on his sole responsibility, conformity with all of the legal requirements necessary to achieve CE marking status. With that mark, the manufacturer is ensuring validity for that product to be sold throughout the EEA. CE marking does not mean that a product was made in the EEA, but states that the product is assessed before being placed on the market. It means the product satisfies the legislative requirements to be sold there.

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.