Publicly available information continues to remain scarce regarding this month’s decision by the General Court of the EU to temporarily suspend the European Commission’s revocation of the EU conditional marketing approval for Ocaliva, Advanz Pharma’s rare liver disease drug.
Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval
Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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A new pilot aims to take Brazil closer to ‘digital transformation.’
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Pharmaceutical companies are being encouraged to reach out to NICE in relation to its HTA Innovation Lab, which provides a sandbox environment in which the health technology assessment body can test new methods of evaluating “innovative and disruptive” therapies.