
Psephos Biomedica
@psephosbio
Psephos is an award winning medical device regulatory, clinical & quality consultancy. Working with clients worldwide we bring medical technologies to market.
ID: 849955067163705346
http://www.psephos.com 06-04-2017 12:00:54
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62 Following

If you are an SME looking for practical advice on navigating the NHS and the HealthTech landscape, join the next Barts Life Sciences NHS Navigation Day tomorrow, which will be online for the first time. To book your place, register here: bit.ly/3O4JcX2

Are you preparing for your Notified Body audits for 2025? Psephos are proud to say that the last 4 Notified Body ISO 13485 / EU MDR audits where we supported clients were completed with very positive outcomes including zero non-conformities. Contact [email protected] for more.





Join Barts Life Sciences for their Final NHS Navigation Day on 18th Feb in person at Queen Mary Enterprise. Irfan Hassan will be one of the experts offering practical advice on regulation for your medical device. Book here: bit.ly/40JRxXk #HealthTech #NHS #AI #MedTech


Visit our website today to read our first newsletter of 2025: psephos.com/newsletters As always, please contact us if you have any regulatory, quality or clinical queries to speak to one of our specialists. [email protected]


We started the year with multiple early-stage clinical investigation submissions, which continues to prove that the UK is a great place to do clinical submissions. Watch our 'Clinical Services' video below and contact us at [email protected] #clinicalinvestigations #regulatory

Join Barts Life Sciences for their Final NHS Navigation Day on 18th Feb in person at Queen Mary Enterprise. Irfan Hassan will be one of the experts offering practical advice on regulation for your medical device. Book here: bit.ly/40JRxXk #HealthTech #NHS #AI #MedTech

Well done to Irfan Hassan & the panel who delivered the final Barts Life Sciences NHS Navigation Day yesterday. It sounds like it was a great session. If you are a Healthtech SME or Innovator and have any regulatory questions, get in touch with us at [email protected] #regulatorycompliance


Non-UK based Medical Device & IVD manufacturers who want to sell in Great Britain (England, Wales & Scotland) must appoint UKRP. The role of a UKRP is to register your device(s) with MHRA, thus ensuring legal & easy access to the Great Britain market. Need a UKRP? [email protected]


Visit our website today to read our Spring newsletter, which includes the latest MHRA updates. psephos.com/newsletters As always, please contact us if you have any regulatory, quality or clinical queries to speak to one of our specialists. [email protected]



Irfan Hassan is looking forward to attending Barts Life Sciences HealthTech SME Project Showcase tonight. Barts Life Sciences has provided free support to over 150 small & medium-sized enterprises, helping them to navigate the NHS & HealthTech landscape. Enjoy the evening! [email protected]