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Saneca Pharma appoints new CEO

Contract development and manufacturing organisation (CDMO) Saneca Pharma has announced the appointment of its new CEO, Richard Král. Richard, who has...

Amgen sets up a FDA Advisory Committee Meeting To Review Potential New Use Of BLINCYTO

Amgen announced that the Oncologic Drugs Advisory Committee of the U.S. FDA will review data supporting the BLINCYTO® (blinatumomab) supplemental Biologics License Application (sBLA)...

AbbVie presents New, Late Breaking Investigational Data at 2018 at AAD Annual meeting

AbbVie  a global research and development-based biopharmaceutical company, today announced it will present new, late-breaking data across investigational medicines and HUMIRA® (adalimumab) at the...

AbbVie raises dividend and buys $10 billion of shares

AbbVie Inc (ABBV.N) said on Thursday its board had approved a $10 billion stock repurchase program, and the drugmaker also increased its quarterly dividend,...

GSK’S Fluarix Tetra (Influenza Vaccine) for ages six months and older RECEIVES European Approval

GSK announced the expanded indication for Fluarix Tetra (Quadrivalent Influenza Vaccine) has been approved in Europe to include adults and now children from six...

GSK submits landmark IMPACT data to European Medicines Agencies for supporting Trelegy Ellipta

GlaxoSmithKline plc and Innoviva, Inc. announced the submission of the landmark IMPACT data to the European Medicines Agency as part of a type II...

FDA approves ODD for selumetinib for treating neurofibromatosis type 1 (NF1): Merck

AstraZeneca and Merck, known as MSD outside the U.S. and Canada, announced that the U.S. FDA has granted Orphan Drug Designation (ODD) for selumetinib,...

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