Webinars
Webinars
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Webinar to provide insight on point of need rapid PCR testing
Medical experts will be offering insights and advice on tackling respiratory infections in the wake of the pandemic during a webinar hosted by medtech innovator QuantuMDx in partnership with Select Science. Read more
28 Jun 2022
Webinar features four Taiwan Excellence Awards winners
On October 14, Taiwan Excellence hosted a webinar on Smart Medical Solutions and Biotesting, welcoming viewers from all over the world. This hour-long webinar featured the winners of this year’s Taiwan Excellence Awards. Read more
9 Nov 2021
Webinar to update current changes to MDR and IVDR
Medilink Midlands will cover an update on the current changes to Medical Device Regulation (MDR), In Vitro Diagnostic Regulation (IVDR) and the role of the person responsible. Read more
14 Oct 2021
Webinar to consider current post-Brexit situation in life sciences
Medilink Midlands will be hosting a webinar with Mills & Reeve to consider the situation in life sciences ten months on after the implementation of the UK’s Brexit deal with the EU. Read more
8 Oct 2021
WEBINAR: How suppliers can support MDR compliance for your medical devices
In this webinar, Thomas Beck and Lee Ferguson discuss Emerson’s solution partner approach and the way they are prepared to support with expertise, infrastructure, and processes. Read more
29 Sep 2021
Webinar to offer chance to inform government policy
Medilink Midlands will be hosting a webinar with the government’s Office for Life Sciences (OLS), who are eager to hear the views of life sciences businesses on what more government can do to support the growth and advancement of the sector. Read more
17 Sep 2021
Webinar to highlight effects of immigration changes
Medilink Midlands will be hosting a webinar in partnership with Make UK to find out what changes companies need to consider in respect of the UK’s new immigration system, and the new relationship with the EU as set out in the UK-EU TCA. Read more
7 Jul 2021
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11 key quality regulation terms to know post-Brexit
Are you a quality manager for a small medical device start-up looking to expand into global markets? Or maybe you are a seasoned device manufacturer preparing to once again traverse quality regulations to deliver a new product to the European market? Read more
White Papers
Testing the EMR and Beyond
Discover how to deliver Exceptional Patient Care through Quality Technology in this whitepaper from Keysight Technologies Read more
White paper highlights clinical evidence required for IVDR
A white paper from RQM+, the regulatory, quality, and clinical consulting firm, aims to provide clarity on the clinical evidence required to comply with the EU IVDR, and spotlights synergies between EU and US requirements. Read more
Avoid false positive results in endotoxin testing
Endotoxins can be a risk to patient safety. Even a low endotoxin concentration in the blood stream can produce inflammation in the human body. endotoxins, frequent and reliable testing for endotoxin levels on medical devices is required. Read more
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How can the UK seize the initiative for healthcare partnerships with the Gulf?
Michael Latham, associate director, Lexington, explains why feels the future of medtech innovation depends on UK-Arab trade relationships. Read more
27 Jan 2023
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Using technology to keep people out of hospital
Sonia Neary from Wellola discusses the appetite for technology for treating conditions, how to keep people out of hospital if possible, the current backlogs being seen by health services and diversity challenges in healthcare. Read more
27 Jan 2023
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Reflections and what lies ahead for life sciences in 2023
Fiona Maini – principal, global compliance and strategy at Medidata, Dassault Systèmes company reflects on the year just gone, and predicts what lies ahead for life sciences. Read more
23 Jan 2023
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Tackling life sciences challenges through collaboration in 2023
Mayer Schreiber, CEO of Discovery Park, looks at the current situation of life sciences and forecasts what steps need to be taken in 2023 to move the sector forward. Read more
18 Jan 2023
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How AI can be used for good
In the first MedTalk Podcast of 2023, Ian Bolland is joined by Zillah Anderson from Faculty AI to discuss the use of data in healthcare, how AI can be used for good, the development of a COVID-19 NHS early warning system, and what 2023 has in store. Read more
16 Jan 2023
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A look at the FDA’s approach to medical device regulations
Chris Harvey, senior vice president of brand protection at Sedgwick, discusses the recall data in the company’s Brand Protection report. Read more
20 Jan 2023
Transfer to manufacture: selecting a partner
Thom Wyatt, principal engineer, Springboard, outlines essential factors for consideration when selecting a contract manufacturer. Read more
18 Jan 2023
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MedTechs need a platform that enables their developers’ talents to blossom
Mike Fuller, regional director of marketing, InterSystems UKI, outlines research suggesting developers could instead be better spending their time working on driving their end products to market, rather than getting caught up in menial data tasks. Read more
17 Jan 2023
Making social value real in the health sector
Jin Sahota and Alan Wain, who have over 20 years' experience in public procurement, address the critical topic of social value. Read more
16 Jan 2023
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2023: out with the old, in with the new?
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, chair of the Urology Trade Association updates readers on key recent announcements impacting the medtech sector in the UK. Read more
6 Jan 2023
White Paper
Testing the EMR and Beyond
Discover how to deliver Exceptional Patient Care through Quality Technology in this whitepaper from Keysight Technologies Read more
Sponsored
Danai Jetawattana Danai - stock.adobe.com
11 key quality regulation terms to know post-Brexit
Are you a quality manager for a small medical device start-up looking to expand into global markets? Or maybe you are a seasoned device manufacturer preparing to once again traverse quality regulations to deliver a new product to the European market? Read more
ProStockStudio Shutterstock
Using technology to keep people out of hospital
Sonia Neary from Wellola discusses the appetite for technology for treating conditions, how to keep people out of hospital if possible, the current backlogs being seen by health services and diversity challenges in healthcare. Read more
Sponsored
Sorry, no results.
ARRANGE A WEBINAR
Drive leads and engagement with a Med-Tech Innovation Webinar
Webinars offer a multi-layered marketing outcome, enabling you to tell your story to a global audience, define your organisation as a thought leader and simultaneously deliver a healthy number of leads for your sales team to get to work on. Read more
