December 17, 2018

Robin Stephens from Psephos Biomedica and Jacques du Preez from Mosaic Surgical presented an EU Medical Device & IVD Regulations - Strategy & Requirements Workshop on Wednesday 12th December in London. The new EU Medical Device Regulation (MDR) is in its implementation...

October 2, 2018

Psephos Biomedica would like to invite you to an evening with the inspirational Janette Benaddi.

Janette Benaddi is a business woman, international speaker and consultant to the life science industries. In 2015 Janette along with 3 other women became the first women to...

October 12, 2017

With the publication of the Medical Device and IVD Regulations earlier this year, as well as ongoing Brexit negotiations, this was definitely a timely event!

ABHI brought together some key speakers expert in their field from industry, Competent Authority and Notified Bo...

September 19, 2017

A strategic approach to developing and commercialising medical devices is becoming ever more valuable.  Not only are many regulatory, quality and clinical milestones significant value inflection points for any company or project, but their long-term success depends on...

August 23, 2017

In today’s global marketplace for medical devices two of the most important regulatory challenges for manufacturers are obtaining the CE Mark in Europe and complying with FDA requirements in the USA.

Psephos has always been able to bring strategic and practical input in...

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