This one-day course is designed for those who need to better understand what medical device audit is, what it is trying to do, how to do it, and when it is required. You might be new to medical devices, about to get involved with internal audit, perhaps you are thinking of becoming an auditor? Perhaps […]
From September 30th this year, it is mandatory to use the PEPPOL standard for orders with the NHS, if you do not have this standard in place your NHS business will be impacted. PEPPOL is the system the NHS has mandated for e-Procurement and e-Invoicing, as well as the international GS1 standard, and enables the […]
Africa Health is the largest healthcare event in the continent and is enjoying year on year growth. The 2018 exhibition is expecting around 10,000 visitors from over 60 countries, including professionals within hospitals, clinics and the government.
Calling all Biotech companies and academia from the Midlands. Are you looking to enter new markets? Are you looking to increase your market share? Are you looking to collaborate with like-minded organisations and academia? Following a successful visit to BIO 2017, Midlands Engine are taking a delegation of Midlands Biotech companies and academia to BIO […]
Big Data, Data Analytics and Artificial Intelligence are becoming so overused that they can mean anything to anyone, however, the hype doesn’t change the facts. Health and Medtech companies are being overwhelmed with data and if you don’t know what to do with it, your competition will. Join BioCity Group for a series of free […]
Attend this free half-day training course on 'Your NICE Submission for Devices and Diagnostics - what you need to know' to learn about: - MedTech and NICE - Your value proposition - Specifying a decision problem for HTA - Generating clinical evidence - Economic evaluation of medical devices The team from NICE (National […]
Clinical strategy, evidence and evaluation are central to product approval and market access. It’s a requirement of the new EU Medical Device Regulation (MDR: article 61) that a medical device company have a regulatory strategy and of the MDR and MEDDEV 2.7/1 rev 4 that the company have a clinical evaluation strategy. In order to […]
This one-day course is designed for those who need to better understand the Medical Device Directive (MDD) and want to learn what is important to understand for compliance in the Medical Device Regulation (MDR). Comprehensive notes in the form of slides are used in the training, but it is the experience, insights, examples and methods […]
The event sits firmly in our calendar of events and is a must-attend event for those in the Life Sciences sector across the East Midlands. The event includes a conference, exhibition, ample networking opportunities and our annual awards.
The 2018 Symposium is your opportunity to learn directly from the clinicians and scientists working as part of the NIHR Nottingham Biomedical Research Centre (BRC). Held for the first time this year, the Symposium will showcase the latest developments from the Nottingham BRC and give you a greater understanding of how their research is being […]
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