Psephos Biomedica

Irfan Hassan is looking forward to attending @ls_barts HealthTech SME Project Showcase tonight. @ls_barts has provided free support to over 150 small & medium-sized enterprises, helping them to navigate the NHS & HealthTech landscape. Enjoy the evening! info@psephos.com

Join us for our next 1/2 day workshop with @SEHTA_UK to unlock Global Market Access: Navigating US FDA and EU CE Marking & demystify the path to #regulatory #compliance for your products. 👉 1st April 2025, London - FREE TO ATTEND bit.ly/4flUEJU #medtech #healthtech

Join us for our next 1/2 day workshop with @SEHTA_UK to unlock Global Market Access: Navigating US FDA and EU CE Marking & demystify the path to #regulatory #compliance for your products. 👉 1st April 2025, London - FREE TO ATTEND bit.ly/4flUEJU #medtech #healthtech

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. info@psephos.com

Irfan Hassan is looking forward to the @MHRAgovuk Innovation Showcase at techUK today. MHRA will be showcasing their most innovative work across areas like cyber security with a focus on their AI prototypes in the regulatory lifecycle. Contact info@psephos.com to find out more.

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? rep@psephos.com

Join us for our next 1/2 day workshop with @SEHTA_UK to unlock Global Market Access: Navigating US FDA and EU CE Marking & demystify the path to #regulatory #compliance for your products. 👉 1st April 2025, London - FREE TO ATTEND bit.ly/4flUEJU #medtech #healthtech

Well done to Irfan Hassan & the panel who delivered the final @ls_barts 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 info@psephos.com #regulatorycompliance

Join @ls_barts 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

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 info@psephos.com #clinicalinvestigations #regulatory

Join us for our next 1/2 day workshop with @SEHTA_UK on ‘Concept to Compliance – A Roadmap to EU & FDA Approval’ to show you how to achieve #regulatory #compliance for your #medicaldevice 👉 1st April 2025, London - FREE TO ATTEND bit.ly/4flUEJU #medtech #healthtech

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. info@psephos.com

Join us for our next 1/2 day workshop with @SEHTA_UK on ‘Concept to Compliance – A Roadmap to EU & FDA Approval’ to show you how to achieve #regulatory #compliance for your #medicaldevice 👉 1st April 2025, London - FREE TO ATTEND bit.ly/4flUEJU #medtech #healthtech

Join @ls_barts 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

Join us for our next workshop ‘Concept to Compliance – A Roadmap to EU and FDA Approval’ to show you how to achieve regulatory compliance for your medical device. Thurs 27th Feb 2025. 10:00-13:00 in London. FREE to attend. REGISTER now bit.ly/4flUEJU

Visit our website to read our final newsletter of 2024: psephos.com/newsletters We wish you all a happy festive season and look forward to continuing our work with our clients and partners in 2025. #medtech #medicaldevices #regulatory #regulatorycompliance #QMS #clinical

Join us for our next workshop ‘Concept to Compliance – A Roadmap to EU and FDA Approval’ to show you how to achieve regulatory compliance for your medical device. Thurs 27th Feb 2025 10:00-13:00 in London. FREE to attend REGISTER now bit.ly/4flUEJU

Join us for our next workshop ‘Concept to Compliance – A Roadmap to EU and FDA Approval’ to show you how to achieve regulatory compliance for your medical device. Thurs 27th Feb 2025 10:00-13:00 in London. FREE to attend REGISTER now bit.ly/4flUEJU

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 info@psephos.com for more.

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