Martin Murphy, Principal Consultant at 42 Technology explains what impact the FDA’s upcoming new regulation will have on drug delivery device developers. The regulatory world of medical devices is undergoing one of the most significant transformations in nearly three decades. The long-standing Quali
Editor Oli Johnson speaks to HiArc President Nate Doemling about the role the company plays in product development for life sciences companies, offering a tactical guide on avoiding common design and regulatory missteps. Earlier this year, HiArc rebranded from its previous name, KMC Systems, as the
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, and advisor to MedTech suppliers, looks at the impact of a major grant from the Wellcome Trust to fund development of new standards for digital mental health apps. UK medical
Elizabeth Norwood, Senior Chemist at MicroCare, LLC, outlines the impact of contamination on optical signal transmission, the role of electrostatic attraction in persistent debris, and the importance of adopting industry-approved inspection and cleaning standards like IEC 61300-3-35. Norwood advocat
Editor Oli Johnson speaks to SPARK TSL CEO Jane Stephenson about the switch from analog to digital in the NHS in the recently published 10 Year Health Plan. Here is the article from Jane that was published on the Med-Tech Insights website earlier this year – https://med-techinsights.com/2025/08/
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, and advisor to MedTech suppliers, reports on recent developments at NHS Supply Chain and their potential implications for suppliers, the NHS, patients, and the wider MedTech
Editor Oli Johnson caught up with Ensera CEO Jason Anderson at COMPAMED 2025 to talk about the brand transformation and the new direction Ensera is taking, as well as the company’s role in the Neupulse device.
Editor Oli Johnson spoke to Dennis Gavranovich and Caroline Herdman of Junkosha about the company’s newly-launched dual layer hybrid channel tubing at COMPAMED 2025.
At COMPAMED 2025, Editor Oli Johnson caught up with BioInteractions‘ Commercial Director Arjun Luthra about the launch of Surface Active Materials, a new category of coatings for medical devices.
Brian Mangan, formerly of NHS Supply Chain and now CEO of Luach Consulting Group sat down with the Medical Technology Group to discuss the NHS’s new value based procurement guidelines How did you come to be involved with value based procurement? NHS Supply Chain said they had a lot of industry comin
Surface measurement expert Dyne Testing, an Intertronics brand, has released a new guide to help medical device manufacturers understand surface energy and tension, and their relationship to adhesion and coatings in MedTech. Why Surface Measurement Matters in Medical Device Manufacturing informs eng
Olivia Friett, editor of FemTech on Med-Tech Insights, spoke to Cyclana Bio‘s CEO, Dr. Léa Wenger, after they announced they had raised £5M to advance drug discovery for Endometriosis. The environment in which you perform your cellular assays matters. The ideal assay is done in an environment that c
