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NINLAROTM (ixazomib) Receives Conditional Approval from the European Commission to Treat Multiple Myeloma

Takeda Pharmaceutical Company Limited announced that the European Commission has granted conditional marketing authorization for NINLAROTM (ixazomib) capsules, indicated in combination with lenalidomide and...

Pharma Parallel Trade: Beyond Brexit and EU Falsified Medicine Directive

Over 90 senior leaders in parallel trade will meet in London in February 2017 to discuss upcoming trends and share best practices.With Brexit and...

Novo Nordisk receives US FDA approval for Xultophy 100/3.6

Novo Nordisk announced that the US FDA has approved the NDA for Xultophy® 100/3.6.Xultophy® 100/3.6 is indicated as an adjunct to diet and exercise...

MedImmune completes out-licensing agreement with Allergan for MEDI2070

AstraZeneca announced the completion of the licensing agreement between MedImmune, its global biologics research and development arm, and Allergan plc, for the global rights...

Largest Ever PACK EXPO Exceeds Highest of Expectations

On the 60th Anniversary of its debut, PACK EXPO International and the co-located Pharma EXPO served as the world’s largest and most comprehensive processing...

Shire launches CUVITRU™ [Immune Globulin Subcutaneous (Human), 20% Solution] in the U.S. for Primary Immunodeficiency

Shire plc announces the launch of CUVITRU , 20% Solution], the first and only Subcutaneous 20% treatment option without proline available in the U.S....

Medivir strengthens its clinical pipeline by entering into agreement to acquire a portfolio of clinical stage oncology programs

Medivir AB announces that it has entered into an agreement to acquire two clinical stage oncology programs from Tetralogic Pharmaceuticals Corporation , advancing and...

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