The Agency expects this initiative to accelerate the implementation of changes to product information and to ensure consistency across EU countries, thus leading to better information for patients on their medicines. Marketing-authorisation holders can use these translations to update their product information. The Agency publishes these translations in all official EU languages, as well as Norwegian and Icelandic, in the table below after review of their quality by the national regulatory authorities in EU Member States. Starting from the January 2015 PRAC meeting, the Agency now publishes recommendations for updates of product information translated into all official European Union (EU) languages. A cumulative list of all signals discussed at the PRAC since September 2012 is also available below. The first list was published in October 2013 and lists the recommendations from the September 2013 PRAC meeting. The doubleCount signal depends on count.Whenever count updates, Angular knows that anything which depends on either count or doubleCount needs to update as well. The overview of PRAC recommendations is published after each month's CHMP and CMDh meeting. Links to many useful web sites Component suppliers on the web Index of recent ICs and link to manufacturers ' sites Electronics engineers network Electronic. contentcopy const count: WritableSignal < number > signal (0) const doubleCount: Signal < number > computed (() > count 2).The adverse event could be a symptom of another illness or caused by another medicine taken by the patient. The presence of a safety signal does not mean that a medicine has caused the reported adverse event. They should monitor the information on this page regularly to keep informed about the PRAC recommendations concerning their products. Marketing-authorisation holders are expected to take action according to the recommendations. It is the responsibility of the medicines regulatory authorities in the Member States to oversee that these PRAC recommendations are adhered to. the Coordination Group for Mutual Recognition and Decentralised Procedures - Human ( CMDh), for information, if the signal concerns a nationally authorised medicine.At the time of publication, the PRAC recommendations have been endorsed by the CHMP
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