CLINICAL TRIALS MASTERCLASS: Start with the end in mind Monday 2 September 12 pm - 4 pm Boardroom | BioCity, Nottingham Presented by NICE, Arthur Gallagher and Remap Consulting If you are a biotech company thinking about selling to a larger pharmaceutical company or going to market alone, it is important that early clinical plans […]

MediWales is collaborating with the West of England Academic Health Science Network (AHSN) to deliver this conference which will focus on monitoring and supporting patients outside the hospital setting (at home, in nursing and care homes) to specifically enable the measurement of vital signs to calculate a Nation Early Warning Score (NEWS) which is used […]

Join Nikki Whitfield, VP, CDMO Services at Quotient Sciences and Claire Thompson, CEO, Agility Health Tech and discover how to transition from your candidate selection process and how to utilize a data driven approach to develop the right dosage forms to achieve proof-of-concept. This webinar will explore screening techniques, integrated approaches and phase-appropriate development strategies. […]

Are you ready for the imminent new medical devices regulations applicable from May 2020? Implementation of the new regulations needs to be a priority for industry. In less than 10 months, medical device regulations are set to change. With such a short timeline, organisations need to act now to ensure minimal disruption to their organisation […]

WHO Patient Safety Day is an annual event on 17th September. For 2019, Loughborough University HFE Hub is collaborating with the Healthcare Safety Investigation Branch (HSIB) to offer this free networking event. Healthcare staff, decision-makers, commissioners, managers and politicians are all invited. 10: 00 Tea/Coffee 10.30 Welcome and Introduction - Sue Hignett & HSIB Director […]

Legal Manufacturers of In Vitro Diagnostic products need to be aware of the scope and implications of the new European In Vitro Diagnostics Regulations 2017/746. Organisations must be realistic and prepared. Not only for the impact of changes in the short-term, but for the long-term implications to the development and maintenance of diagnostic products in […]

Wednesday 16th October 2019 Hill Dickinson, Broadgate Tower, 20 Primrose Street, London EC2A 2EW, 10:30 – 16:00 SEHTA members fee - £250 + VAT per delegate SEHTA non-members fee - £300 + VAT per delegate Why attend Clinical strategy, evidence and evaluation are central to product approval and market access. Through clinical data a company […]

This seminar will provide you insights into the key regulatory changes of the IVDR, to help you to prepare your organisation and your devices for IVDR compliance. Cost: SEHTA members fee: £240 + VAT / Non-Members: £280 + VAT per delegate Not a member of SEHTA? It's free to join - just click here The […]

UK HealthTech brings together key speakers to discuss the major strategic issues and policy developments facing the life science and health technology sector. This years themes will include sessions relating to: - Regulatory updates - Investor Workshops - Finance and Funding seminars - Support for spin out and early stage companies - NHS Access talks […]

Are you an innovator working in mHealth? SEHTA and ORCHA are organising our 2nd mHealth of 2019 on App Development on Wednesday 11th December in London. This workshop aims to give developers clear guidance on exactly what mHealth innovators will need to do as an organisation to prepare for and conform to these regulations to ensure the transition is as […]