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The European Commission’s (EC’s) Directorate-General for Health and Food Safety recently published a survey of notified bodies. This was conducted between April and May 2023, eliciting responses from all 39 notified bodies designated under the Medical Devices Regulation (MDR) and 10 Notified bodies designated under the In Vitro Diagnostic Regulation (IVDR).
From July 1, tourists travelling to Thailand will only need to show a vaccination certificate or a negative Covid-19 test, the government announced on Friday, along with a decision to lift the requirement to wear a face mask in public spaces.
In a post shared on Reddit, a hall ticket read the following words in its instruction section: Do not remove your face mark when inside the examination centre.
The DNA sequencing giant Illumina has launched a new in vitro diagnostic test in Europe designed to profile various cancer mutations and help direct patients to targeted therapies.
Following an LFA verification of a Recipient’s procurement, the QA Team would like to bring to the attention of the procurement community that certain Personal Protective Equipment (PPE) products and medical devices, and related documents, prominently display the CE mark logo whereas the products have not been verified as meeting European procedures.