The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior...
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ensuring that medicines and medical devices work and are acceptably safe. The MHRA was formed in 2003 with the merger of the Medicines Control Agency (MCA) and...
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European Medicines Agency (EMA). 29 January 2020. Archived from the original on 14 August 2020. Retrieved 26 September 2020. "Wegovy EPAR". European Medicines...
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similar model to that of the European Medicines Agency, it is intended to have a wide scope covering medicines, traditional medicine, and medical devices. The...
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responsible for the regulatory activity of pharmaceuticals in Italy. European Medicines Agency Istituto Superiore di Sanità Official website v t e v t e...
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Biosimilar (section European Union)
their lifecycle. Drug-related authorities such as the European Medicines Agency (EMA) of the European Union, the United States Food and Drug Administration...
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© European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "Dapagliflozin Viatris EPAR". European Medicines Agency. 4...
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and methods of analysis for medicines. These standards apply to medicines for both human and veterinary use. The European Pharmacopoeia has a legally...
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N-Nitrosodimethylamine (section European Union)
is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "Nitrosamine impurities". European Medicines Agency (EMA)...
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Approximately 180 people work at the agency; most are pharmacists and doctors. Regulation of therapeutic goods European Medicines Agency Official website v t e v...
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Adalimumab (category World Health Organization essential medicines)
EPAR". European Medicines Agency (EMA). 14 September 2021. Archived from the original on 24 April 2022. Retrieved 23 April 2022. "Hulio EPAR". European Medicines...
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The European Directorate for the Quality of Medicines & HealthCare (EDQM) is a Directorate and partial agreement of the Council of Europe that traces...
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which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "Synflorix EPAR". European Medicines Agency (EMA). 17...
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Director of the European Medicines Agency (EMA) since November 2020. She is also the chairperson at the International Coalition of Medicines Regulatory Authorities...
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vaccine has since been approved by several medicine agencies worldwide, such as the European Medicines Agency (EMA), and the Australian Therapeutic Goods...
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the brand name Zepbound. In November 2023, the UK Medicines and Healthcare products Regulatory Agency revised the indication for tirzepatide to include...
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European Medicines Agency in the European Union. In January 2018, the Committee for Medicinal Products for Human Use of the European Medicines Agency...
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H-W-2495". European Medicines Agency (EMA). Archived from the original on 2 October 2018. Retrieved 28 June 2018. "Hexyon EPAR". European Medicines Agency (EMA)...
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copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "Livogiva EPAR". European Medicines Agency (EMA). 26...
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(Press release). European Medicines Agency. 6 January 2021. Archived from the original on 17 March 2021. Retrieved 6 January 2021. "European Commission authorises...
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code itself is issued by the Medicines and Healthcare products Regulatory Agency in the UK and the European Medicines Agency. "Martin Lewis: A drugs bust...
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viral infections. The most common side effects reported by the European Medicines Agency (EMA) include injection-site reactions (such as redness, swelling...
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EPAR". European Medicines Agency. 13 March 2024. Retrieved 20 March 2024. Text was copied from this source which is copyright European Medicines Agency. Reproduction...
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which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "First-in-class medicine recommended for treatment...
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use, a new chemical entity to patients." Because of this, the European Medicines Agency (EMA) initially had not considered teriflunomide to be a new active...
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European Medicines Agency (EMA). 17 September 2018. Retrieved 21 August 2020. Text was copied from this source which is © European Medicines Agency....
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European Medicines Agency (EMA) started reviewing its position at the request of the French ANSM, which withdrew all pholcodine-containing medicines after...
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with COPD, including chronic bronchitis and emphysema, and the European Medicines Agency approved it as a second-line therapy for the treatment of COPD...
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Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of...
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which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged. "Opzelura EPAR". European Medicines Agency. 20 April...
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