The "European FDA," the EMA is responsible for protecting public health by mobilizing scientific resources within the European Union, promoting health care through the regulation of new pharmaceuticals, and supporting the pharmaceutical R&D industry by developing efficient, effective and responsive operating procedures. Formerly European Agency for the Evaluation of Medicinal Products (EMEA).
Glossary
European Medicines Agency (EMA)
02.27.12
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Breaking News | Industry News
J&J Releases COVID-Vax Booster Data
Interim data from these studies demonstrate that a booster dose of the vaccine generated a rapid and robust increase in spike-binding antibodies.
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APIs | Breaking News | cGMP Manufacture | Industry News
MediPharm Labs Receives Canadian GMP Pharmaceutical DEL
License can be used for manufacturing, testing and sale of APIs and pharmaceutical drug products containing cannabis.
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Biologics, Proteins, Vaccines | Clinical Trials | Drug Development
Gene Therapy Trials
Critical regulatory and study start-up questions for gene therapy trials in the U.S., UK, and Europe.April Marquick, Cell and Gene Therapy Expert, Premier Research
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Bio News | Breaking News | Collaborations & Alliances | Industry News
BioVaxys Inks Deal with CDMO BioElpida
Includes clinical-grade bioproduction and aseptic packaging for ovarian cancer vaccine candidate BXV-0918A.Tim Wright, Editor, Contract Pharma
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Breaking News | cGMP Manufacture | Industry News
EMA Approves BioNTech's COVID Vax Production at Marburg Site
Largest mRNA vaccine manufacturing site in Europe has annual production capacity of up to one billion doses of its COVID-19 vaccine.Kristin Brooks
