Our specialist team here at JensonR+ is experienced in regulatory affairs, product development, quality assurance, drug safety, medical information, copy approval, project management, training and market access.

Here we share insights into our ways of thinking in this changing landscape. Any questions please talk to us, we are happy to start the conversation.

CEE Bill

By |May 3rd, 2022|

Earth day may have past, but we should not lose sight of the need to protect and help the planet we all live on – our home. In the UK there is a Private Members Bill going through parliament - The Climate & Ecological Emergency Bill.

New guidance on borderline between medical devices and medicinal products

By |April 27th, 2022|

A significant and useful new guidance document on the borderline between medical devices and medicinal products under Regulation (EU) 2017/745 on medical devices has just been endorsed by the Medical Device Coordination Group (MDCG 2022-5 ).

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