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India developing 7 more indigenous Covid-19 vaccines

Union health minister Harsh Vardhan has said that the country is developing seven more Covid-19 vaccines to make them available to every citizen of India. “We are currently administering the Covishield and Covaxin vaccines to healthcare and frontline workers. The...

China approves Sinovac’s coronavirus vaccine

China’s national regulator has approved Sinovac Biotech’s COVID-19 vaccine for use by the general public. This is the second vaccine approved by China’s National Medical Products Administration (NMPA). Both of the vaccines, along with another experimental vaccine from Sinopharm, have...

Merck and BioNTech to boost lipid supply for Covid-19 vaccine production

Merck and BioNTech have announced a further expansion of their strategic partnership to accelerate the supply of urgently needed lipids and boost the amount of their delivery by the year-end. The lipids will be used for producing the Pfizer and...

Effective COVID-19 Vaccine Air Transportation and Handling Requires An Air Cargo Community Approach

TIACA and Pharma.Aero jointly release their second report for the global air cargo and pharmaceutical industries outlining recommended practices and insights for effective COVID-19 vaccine air transportation and handling. The report reinforces that COVID-19 vaccines are of high value and...

Europital board forewarns that clinical deficits to slow biotech development in 2021

The newly formed Scientific Advisory Board (SAB) of Europital – a globally-focused, full-service CRO serving small and mid-tier innovators – forewarns that a clinical knowledge deficit amongst smaller biotechs will potentially slow trials in 2021. The Europital SAB, comprises a...

Pharmaceutical outsourcing partner predicts AI and dialogue cues will assist HCP engagement

How can pharmaceutical companies leverage digital to engage HCPs in a complex healthcare environment? Digital transformation has been the leading topic of discussion in most industries this year, and healthcare is no exception. Although, it would be unfair to dismiss...

U.S. FDA Approves BMS’s Breyanzi, a New CAR T Cell Therapy for Adults with Relapsed or Refractory Large B-cell Lymphoma

Bristol Myers Squibb announced that the U.S. FDA has approved Breyanzi, a CD19-directed chimeric antigen receptor (CAR) T cell therapy for the treatment of adult patients with relapsed or refractory (R/R) large B-cell lymphoma (LBCL) after two or more...

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