Cell Viability Assays Market- Roadmap for Recovery From COVID-19 | Focus On Timely Diagnosis Of Diseases to Boost the Market Growth | Technavio -…

LONDON--(BUSINESS WIRE)--Technavio has been monitoring the cell viability assays market and it is poised to grow by USD 1.40 bn during 2020-2024, progressing at a CAGR of over 8% during the forecast period. The report offers an up-to-date analysis regarding the current market scenario, latest trends and drivers, and the overall market environment. Although the COVID-19 pandemic continues to transform the growth of various industries, the immediate impact of the outbreak is varied.

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Global Stem Cell Therapy for Diabetes and Related Conditions Market Latest Innovations and Forecast 2021-2026 : Athersys, Mesoblast, Caladrius…

The Stem Cell Therapy for Diabetes and Related Conditions Market report includes an in-depth analysis of the global Stem Cell Therapy for Diabetes and Related Conditions market for the present as well as forecast period. The report encompasses the competition landscape entailing share analysis of the key players in the Stem Cell Therapy for Diabetes and Related Conditions market based on their revenues and other significant factors.

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Stem Cell Therapy Market Size, Analytical Overview, Key Players, Growth Factors, Demand, Trends And Forecast to 2027 – The Daily Chronicle

Fort Collins, Colorado Reports Globe recently added the Stem Cell Therapy Market Research Report that provides a thorough investigation of the market scenario of the market size, share, demand, growth, trends, and forecast from 2020-2027. The report covers the impact analysis of the COVID-19 pandemic

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FDA Grants RMAT Designation to MultiStem Cell Therapy for the Treatment of Acute Respiratory Distress Syndrome – BioSpace

Sept. 23, 2020 10:00 UTC CLEVELAND--(BUSINESS WIRE)-- Athersys, Inc., a leading regenerative medicine company in late-stage clinical development, announced today that MultiStem cell therapy was granted Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration (FDA) for the acute respiratory distress syndrome (ARDS) program

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