Rinvoq (upadacitinib) receives U.S. FDA approval for active psoriatic arthritis

14 December 2021 - Milestone marks the second FDA approved indication for Rinvoq following rheumatoid arthritis in 2019. ...

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Heterogeneity of treatment effect; estimating how the effects of interventions vary across individuals

14 December 2021 -  ...

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TG Therapeutics announces FDA acceptance of biologics license application for ublituximab as a treatment for patients with relapsing forms of multiple sclerosis

14 December 2021 - Prescription Drug User Fee Act goal date of 28 September 2022. ...

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EMA reviewing new data on effectiveness of Lagevrio (molnupiravir) for the treatment of COVID-19

14 December 2021 - Following EMA’s interim recommendations to support national authorities who may decide on early use of Lagevrio ...

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FDA publishes discussion paper and seeks public input on 3D printing of medical devices at the point of care

10 December 2021 - Today, the U.S. FDA published a discussion paper regarding 3D printing medical devices at the point of ...

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Access Consortium statement on COVID-19 medicines

14 December 2021 - Vaccines have played a critical role in fighting the COVID-19 pandemic. However, medicines can still play ...

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Galderma receives FDA approval for new Sculptra label, offering more options to aesthetic partners

13 December 2021 - New label update allows for immediate use after reconstitution and more convenient administration of Sculptra with the ...

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mRNA manufacturing facility will deliver long term health benefits for Australians

14 December 2021 - Medicines Australia welcomes the announcement that Australia will manufacture mRNA vaccines in a deal struck with ...

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EMA publishes agenda for 13-16 CHMP meeting

13 December 2021 - The EMA has published a draft agenda for this week's CHMP meeting. ...

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Veru announces FDA approval of Entadfi, a new treatment for benign prostatic hyperplasia

13 December 2021 - Commercialisation will start early calendar year 2022. ...

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Pfizer/BioNTech vaccine approved for children by Swiss regulator

10 December 2021 - The Swiss medical regulator has approved the use of Pfizer/BioNTech’s Covid-19 vaccine for children aged five to ...

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InterVene’s BlueLeaf Endovenous Valve Formation System granted breakthrough device designation by the FDA

13 December 2021 - InterVene announced today that it has received breakthrough device designation by the FDA for the company’s BlueLeaf ...

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Moderna vaccine deal to produce 100 million doses in Melbourne reached by Federal and Victorian Governments

13 December 2021 - Australia is poised to become the largest producer of mRNA vac­cines outside the US and Europe ...

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European Commission approves Pfizer's Cibinqo (abrocitinib) for the treatment of adults with moderate to severe atopic dermatitis

10 December 2021 - Cibinqo is a once daily oral treatment with proven efficacy demonstrated in a large scale clinical ...

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International regulators recommend use of remote inspections as complementary tool beyond pandemic

13 December 2021 - Remote inspections have been useful in maintaining regulatory oversight during the COVID-19 pandemic, but cannot fully replace ...

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