Renata Pharmaceuticals (Ireland) Limited, a subsidiary of Renata Limited in Europe, has received regulatory approval from the European Union (EU) and German authorities for its anti-Parkinson’s therapy, Cabergoletten 1mg and Cabergoletten 2mg. This marks the first of many approvals the company anticipates from the German Federal Institute for Drugs and Medical Devices (BfArM). Renata has a strong presence in the pharmaceutical markets of various countries, including Australia, the USA, Canada, the UK, and the EU, with over 25 approved products. With 64 bioequivalent products and operations in 40 countries, Renata emphasizes research and development, conducts clinical trials, and boasts 14 advanced manufacturing facilities. The company has successfully entered the EU and UK markets, and its global pharmaceutical footprint continues to expand, with plans to enter France, Norway, Denmark, Sweden, Spain, and Portugal.
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