Independent termination as Notified Body for MDR (Medical Device Regulation EU 2017/745) per 31st of October 2019
On behalf of the European Commission, Notified Bodies for medical devices are subject to Joint Assessments with the aim of
On behalf of the European Commission, Notified Bodies for medical devices are subject to Joint Assessments with the aim of
The ISO 22000:2018 standard was published in June 2018. It will replace ISO 22000:2005. Existing certificates according to ISO 22000:2005
We have the pleasure, to inform you the accreditation of ISO 13485: 2016 is valid now.
Beware of fake certificates, not issued from QS Zürich AG, distinguishing feature is the e-mail address: info@latcert.com. We do not work