Devicia, Clarvin, Kickfile, Lea Reg, and Limulus Bio enhance Veranex's European footprint and create control, clinical, and quality service divisions in conjunction with the company's fresh acquisition of Medidee.
By accumulating knowledge of biological evaluations and medical device programs, as well as growing infrastructure, and assigning individuals to act on behalf of the EU and the UK, Veranex's medical device regulation (MDR) and in vitro diagnostic regulation (IVDR) strategy will in turn reap the benefits.
“Devicia, Clarvin, Kickfile, Lea Reg, and Limulus Bio enhance Veranex's European footprint“
David Dockhorn, Chief Executive Officer of Veranex, explained that “this group of companies, led by Devicia and Clarvin, shares the same goal as Veranex” which is “working with our clients to achieve and accelerate medtech innovation.”
These companies “all focus exclusively on medical devices and IVD, providing strategic guidance and informed execution across a number of areas, including clinical trial, medical writing, regulatory strategies, toxicology assessments, designated local representation, and system technologies that bolster Veranex’s full-service medtech capabilities and solutions.”
The acquisitions mean that Veranex's worldwide network can add three mores countries to its portfolio in Europe and the United States.
Chief Executive Officer of Devicia, Elisabeth Liljensten, expressed her excitement regarding “the opportunity to support clients even more comprehensively with our full-service medical device and IVD services, and a significantly stronger global presence. We strongly believe that a global perspective and broad geographic footprint provides strategic value to market access for our clients.”
Chief Executive Officer of Clarvin, Åsa Runnäs, described their shared vision as finding “the best way to help our clients — with a combination of top regulatory intelligence, expert knowledge within different areas, and true global reach.”
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