Connector systems supplier to exhibit at Medical Technology Ireland
Connector systems supplier ODU is exhibiting at Medical Technology Ireland in September.
View ArticleWhitepaper highlights how COVID-19 has affected compliance
Regulatory and compliance consultancy, Maetrics, has released a whitepaper highlighting how the COVID-19 pandemic is affecting regulatory and quality compliance in the life science sector.
View ArticleHow to build a medtech cleanroom in just 4-6 weeks
The pandemic has led to medtech firms needing to rapidly upscale production environments for products experiencing a surge in demand and the R&D of new products. This whitepaper explains how...
View ArticleSocial care technology provider highlights benefits of digital innovation
Social care technology company HAS Technology has launched its latest white paper showcasing the benefits of digital innovation in supporting people throughout their care pathway.
View ArticleIntertronics roundtable discusses what makes a good adhesives partner
To help companies pinpoint what to look for in an adhesives partner, Intertronics has written up the results of a roundtable discussing the question: what makes a good adhesives partner?
View ArticleHow In Silico Medicine Can Accelerate Innovation in Medical Devices
In this white paper Dr. Visa Suomi, Medical Devices Industry Manager at MathWorks, discusses how medtech companies can take advantage of computational modelling and simulation in medical devices...
View ArticleWhite 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...
View ArticlePredicting problems in diagnostics development
With the increased market need for diagnostic devices and the consequent requirement for an expedited development pathway, it is inevitable that many innovations will stumble upon unidentified pitfalls...
View ArticleYour guide to the process of developing diagnostics devices
In this white paper from EG Technology we look at likely pitfalls in the development pathway, and how to create a blueprint so that you can work towards the smoothest route to market.
View ArticleThe four most important AI trends in the medical technology industry
This white paper from Advantech outlines four key trends to consider in your end-to-end solution to ensure that devices are constantly being adapted to new AI options in an efficient and cost-effective...
View ArticleDeveloping safe medical equipment with EMC
EMC is not only mandatory in medical technology. If wireless communication between medical applications gets disrupted, it can have serious consequences for the patient.
View ArticleAvoid 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...
View ArticleMeasure solid content of latex for medical devices in about a minute!
The fast, reliable determination of total solid content of latex precursors is critical for processing medical devices. This white paper explains how to develop a method to determine the total solid...
View ArticleTesting the EMR and Beyond
Discover how to deliver Exceptional Patient Care through Quality Technology in this whitepaper from Keysight Technologies
View ArticleSmaller, safer medical devices require a next generation thermal system
Home medical devices must meet higher safety standards. This whitepaper explains how thermal solutions can improve performance and meet those standards, but they will need to be designed using a system...
View ArticleHow the cobas t 711 coagulation analyser can streamline workflow
The cobas t 711 coagulation analyzer utilizes a W.A.R.M. concept and has demonstrated accurate and reproducible sample measurement in routine practice. Roche explored how the W.A.R.M. concept can...
View ArticleThe Role of PCR Testing in Transplant Infections Management
The role of clinical laboratories and the testing options they provide to aid in screening, diagnosis and treatment response monitoring of infected transplant patients is essential for improving...
View ArticleMedical device regulations: a step forward for patient safety or a step...
How medical device registries can promote both safety and innovation in a new regulatory landscape.
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