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Author: Ema Suárez

• Ratings 7,1 of 10 Stars
• 
• Release Date 2020
• UK
• Abstract In 1800s England, a well meaning but selfish young woman meddles in the love lives of her friends
• Eleanor Catton

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Update on nitrosamines in EU medicines Update Nitrosamines EU and national authorities are continuing their work to prevent and manage the presence of nitrosamine impurities in EU medicines. CHMP highlights: February 2020 MEDICINES COMMITTEES EMA’s human medicines committee (CHMP) recommended two medicines for approval at its 24-27-February meeting. New video launched: How does EMA support SMEs? SMEs Video EMA has prepared and published a short video in German, French, Italian, Spanish, Polish and Portuguese to explain how its dedicated office for small and medium enterprises helps SMEs across Europe. EMA to support development of vaccines and treatments for novel coronavirus disease (COVID-19) Public health Novel coronavirus To contribute to the global response to the outbreak of the novel coronavirus infections, EMA is taking concrete actions to accelerate the development and availability of medicinal products for the treatment and prevention of the new coronavirus. Search for medicines Search for information on human, veterinary or herbal medicines. What's new Find all the latest news and updates published on this website in one place. FAQs Find answers to the most frequently asked questions we receive. Latest news List item 04/03/2020 Emiel van Galen elected as chair of the Committee for Herbal Medicinal Products At its March meeting, EMA’s Committee for Herbal Medicinal Products (HMPC) elected Dr Emiel van Galen as its chair, for a three-year mandate. Dr van Galen is the Head of Department for Botanicals and Novel Foods at the Medicines Evaluation Board (... 03/03/2020 EU and national authorities are continuing their work to prevent and manage the presence of nitrosamine impurities in EU medicines. Nitrosamines are classified as probable human carcinogens (substances that could cause cancer) based on animal... 02/03/2020 EMA organisational changes come into effect As of today, Monday, 2 March, EMA has implemented changes to its organisational structure. The purpose of the re-organisation is to ensure that the Agency operates as efficiently as possible to deliver high quality outputs for public and animal... 28/02/2020 Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 24-27 February 2020 Two new medicines recommended for approval EMA’s human medicines committee (CHMP) recommended two medicines for approval at its February 2020 meeting. The Committee recommended granting a marketing authorisation for Fetcroja (cefiderocol) for the... 21/02/2020 Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 18-20 February 2020 CVMP opinions on veterinary medicinal products The Committee adopted by consensus a positive opinion for an initial marketing authorisation application for Vectormune FP ILT + AE, from Ceva-Phylaxia Co. Ltd, a new vaccine for the active... 14/02/2020 Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 10-13 February 2020 PRAC recommends restrictions in use of cyproterone due to meningioma risk Following a review of the risk of meningioma (a rare tumour of the membranes covering the brain and spinal cord) in patients taking cyproterone, EMA’s safety committee (PRAC)... Load more news Information for Patients and carers Featured news and updates for patients and carers Healthcare professionals Featured news and updates for healthcare professionals, including doctors, nurses and pharmacists Animal health professionals Featured news and updates for animal health professionals and users of veterinary medicines such as pet owners Pharmaceutical industry Featured news and updates for pharmaceutical industry stakeholders active in the human and veterinary medicines fields Media Featured news and updates for journalists with a professional interest in the development and availability of medicines in the European Union Academia Featured news and updates for European academics and researchers in the field of medicine development Key content Product emergency hotline UK’s withdrawal from the EU PRIME: Priority medicines Pharmacovigilance (safety monitoring) Data on medicines Clinical data publication Careers Services & databases Account Management portal eSubmission EudraVigilance (human) EU Veterinary Medicinal Product Database Suspected adverse drug reactions database Clinical data SPOR data management services Service Desk IRIS platform Public register of parallel distribution notices How does EMA work? What we do Our role in authorisation of medicines Who we are Our scientific experts How we work What we publish.

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