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Bristol Myers Squibb Receives Positive CHMP Opinion for Inrebic for Adult Patients with Newly Diagnosed and Previously Treated Myelofibrosis

Bristol Myers Squibb announced the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended approval of Inrebic® (fedratinib)...

First COVID-19 vaccine shipments arrive in Canada, more en route

Some of the country's initial 30,000 doses of the Pfizer-BioNTech vaccines touched down on Sunday night, Prime Minister Justin Trudeau announced on Twitter, sharing a...

Novartis provides update on RUXCOVID study of ruxolitinib for hospitalized patients with COVID-19

Novartis announced that the Phase III RUXCOVID study evaluating ruxolitinib on top of standard of care (SoC) therapy compared to SoC treatment alone in patients...

Saudi Arabia approves Pfizer-BioNTech coronavirus vaccine

Saudi Arabia approved the use of the Pfizer-BioNTech novel coronavirus vaccine, state media reported, becoming the second Gulf country after Bahrain to green-light the drug. "The...

ERT and Bioclinica to Merge, Creating a Global Leader in Clinical Trial Endpoint Technology

ERT, a global leader in clinical end-point data solutions, announced that Bioclinica, a technological and scientific leader in clinical imaging, has agreed to merge with...

Sinovac snags $515M investment to double COVID-19 vaccine capacity as phase 3 readout nears

As the various COVID-19 vaccines move closer to the finish line, their developers have been raising money from investors or through advance government purchases to...

Sinovac Announces Product License for 23-Valent Pneumococcal Polysaccharide Vaccine

Sinovac Biotech Ltd., a leading provider of biopharmaceutical products in China, announced that the China National Medical Products Administration (NMPA) has approved and issued a...

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