The global population is now on the edge of a major shift in healthcare access, delivery and engagement. It is time to adapt or crash.
TORONTO (PRWEB) January 07, 2021
2021 has the potential to be a record year for orphan drugs and advanced therapy medicinal products (ATMPs) in Europe. With the hope of a world in which COVID-19 is a manageable disease comes the promise of ground-breaking new therapies and innovative approaches to digital healthcare. However, these will enter into an access environment under turmoil and change: a new EU Pharmaceutical Strategy, potential changes to orphan drug legislation and continual evolution of health technology assessment (HTA) processes and digital healthcare. The global population is now on the edge of a major shift in healthcare access, delivery and engagement. It is time to adapt or crash.
In this webinar, the featured speakers will bring a fresh, forward-looking perspective to the changing regulatory environment in Europe for orphan drugs and ATMPs and the key access trends expected in 2021. Through a mix of case examples and direct experiences, they will highlight insights into likely changes as a result of a greater number of ATMPs seeking commercialization, the EU Pharmaceutical Strategy and associated changes to the orphan drug legislation. Importantly, the webinar panelists will recommend key considerations for manufacturers to optimize preparation of future orphan drug and ATMP launches.
Join Alexander Natz, EUCOPE Secretary General; and Sophie Schmitz, Managing Partner, Partners4Access, in a live webinar on Wednesday, January 13 at 11am EST (4pm GMT/UK) to gain valuable insights into changes to the regulatory landscape expected in the coming year and advice on how sponsors can optimize their commercialization strategy for orphan drugs and ATMPs in Europe.
For more information, or to register for this event, visit EU Market Access 2021: What’s in Store for Orphan Drugs and ATMPs?
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