The United Kingdom has been building its own regulatory framework to approve and assess drugs post-Brexit. But pharma’s appetite for navigating multiple health technology assessments for its therapies in Europe remains unclear. In next month’s issue, we take a look at how things have changed in the last few years, and what can be expected in the near future.
The September issue will also feature a quantitative look at partial orphan drugs—those expensive therapies that are first approved to treat rare disorders, and then have their labels expanded to include common chronic conditions.
All this plus the latest trends and innovations in the pharma industry, as well as up-to-date analysis and insight from GlobalData experts.
Editor | Manasi Vaidya
Writers | Adam Zamecnik, Irena Maragkou, William Newton, Manasi Vaidya, Urtė Fultinavičiūtė
Magazine Designer | Will Ingham
Graphic Designers | Anett Arc, Ashley McPherson, Tyrrell Lowe, Noemi Balint, Martina Labaiova
Lead Designer | John Hammond
Publisher | Susanne Hauner
Sales Manager | Tom McCormick
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