Manufacturers lobby US Congress for assistance to develop orphan products
This article was originally published in Clinica
Executive Summary
The US Medical Device Manufacturers Association (MDMA) last week called for legislation to speed up the development of medical devices for diagnosing and treating rare disorders. The concept is similar to the 1983 Orphan Drug Act that has successfully led to advances in pharmaceutical treatments for rare diseases.
You may also be interested in...
EU Regulatory Assessors Get AI Boost In Reaching Scientific Decisions
The European Medicines Agency is training scientific staff working for the European medicines regulatory network in how to use a new AI-powered search engine that allows them to easily retrieve information on regulatory precedents.
EU Parliament Stricter Than Council On Medicines And Medical Devices Packaging
The EU Parliament's Environment, Public Health and Food Safety committee takes a compromise position with regards to the Packaging and Packaging Waste Directive. Medicines and medical devices should be exempt, but only until 2035, at which point the European Commission should check whether the development of materials and the recycling process have progressed, and may adjust this exemption accordingly.
Stay Or Exit? Global Health Players Ponder New China Trajectory
It's again the time of year when global CEOs descend on China's capital to discuss strategies. This year, however, the mood is different.