Liability Risks and Litigation Defenses for COVID-19 Tests: Potential Claims and Defenses
Part one of this series looks at the claims brought against manufacturers of diagnostic test kits.
Part one of this series looks at the claims brought against manufacturers of diagnostic test kits.
Companies can improve their chances for a successful transition by leveraging their knowledge of their medical devices and understanding what each device’s categorization under the MDR means to its testing strategy.
New health-related data is arriving almost daily. Making sense of it all is a huge challenge.
Although medical device manufacturers have more time to prepare due to the delayed EU MDR deadline, this shouldn’t distract from the extensive documentation they must compile in the meantime to prove their devices are compliant.
During the current operating environment there has been an increased need for healthcare training using patient simulators for students and practicing healthcare professionals.
During product development, collaboration between software, hardware and quality teams must be tracked and seamless to meet the increasing pace of market demand.
In order to meet the worldwide need for faster and affordable testing processes, companies must shift goals and apply resources to ending this pandemic.
In general, the Asian markets have controlled the COVID-19 virus successfully outside of China, but its effect has still led to new developments and trends.
Across our industry, IoMT will enable us to conduct research in ways that would never previously have been possible.
AdvaMed’s Diagnostic Supply Registry is tracking the progress of molecular diagnostic tests to help support state and federal governments.