With April 1 as the starting point, Horizon Therapeutics expects to put a stop to the supply issues which have affected the company's new and highly popular launch Tepezza since December last year, which the firm states in a press release.
The firm's solution, as it turns out, is that it has received approval from the US Food and Drug Administration (FDA) to introduce a new production setup, which allows Horizon Therapeutics to produce more of the drug itself, rather than outsourcing this task to contractors.
Already a subscriber? Log in.
Read the whole article
Get access for 14 days for free.
No credit card is needed, and you will not be automatically signed up for a paid subscription after the free trial.
- Access all locked articles
- Receive our daily newsletters
- Access our app
Get full access for you and your coworkers.
Start a free company trial todayMore from MedWatch
Fruergaard leveraging experience from Danish partnerships in key roles in Brussels
Experiences from Danish climate partnerships are among the tools that can be leveraged when Novo Nordisk CEO Lars Fruergaard begins stepping up efforts in the life science sector’s central organs in Brussels. ”I’ve been fired up by the intimacy and shared vision we could see in Denmark,” he tells MedWatch.
Stallergenes slapped with injunction
There are still issues with Stallergenes Greer’s factory in Antony, the Agence Nationale de Sécurité du Médicament has concluded.
Overview: Pharma giants and Bavarian Nordic fight over billion-dollar vaccine market
There is currently no approved vaccine for RSV, which causes serious illness and can be deadly for newborns and the elderly. The race to come first to the vaccine market is heating up, while more companies are close to completing phase III studies. Get an overview of their progress here.
Eargo raises USD 100m from investment firm
US-based Eargo, which is run by a Dane, has entered an agreement with an investment firm which is injecting USD 100m into the company.
US authorities expand monkeypox vaccine plan
More Americans will be offered a monkeypox vaccine.
Corporate Quality Compliance Specialists 
Medical Advisor 
QA Specialist for Product Equipment Qualification 
Senior Manager/Associate Director, Global Regulatory Affairs, CMC 
KLIFO is looking for a Project Director for our office in Denmark or Germany or Sweden 
Senior Project Manager (GMP - Life Science) 
Scientific Writer 
Regulatory Affairs Manager - Maternity Cover 
Principal Scientist – Pharmacology 
Global Product Manager - Pulmonology 
Quality Management System Compliance Department Manager 
Nordic Medical Advisor 
Clinical Project Leader/ Sr. Clinical Trial Manager – make a difference and join our mission to bring our IL-22 lead program to patients 
Senior Toxicologist