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FDA chief Hahn walks back plasma claims, but his correction still missed the mark, experts say
August 26, 2020With the emergency use authorization (EUA) for convalescent plasma to treat COVID-19, the FDA and Commissioner Stephen Hahn, M.D., touched off a controversy—particularly about his presentation of the evidence and the political pressure from the White Hous -
Implandata Successfully Gains CE Mark for its EYEMATE System for an Orphan Eye Indication
May 05, 2019Implandata Successfully Gains CE Mark for its EYEMATE System for an Orphan Eye Indication. -
Digital manufacturing is a top priority for life sciences
December 03, 2018The company conducted a survey of business and operational leaders across the life science sector on the trends and technologies that may revolutionise the industry over the coming years.
Pharma Sources Insight January 2025
