Oprava nařízení Evropského parlamentu a Rady (EU) č. 1235/2010 ze dne 15. prosince 2010, kterým se mění, pokud jde o farmakovigilanci humánních léčivých přípravků, nařízení (ES) č. 726/2004, kterým se stanoví postupy Společenství pro registraci humánních a veterinárních léčivých přípravků a dozor nad nimi a kterým se zřizuje Evropská agentura pro léčivé přípravky, a nařízení (ES) č. 1394/2007 o léčivých přípravcích pro moderní terapii (Úřední věstník Evropské unie L 348 ze dne 31. prosince 2010)

Corrigendum to Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products (Official Journal of the European Union L 348 of 31 December 2010 )

On page 6, Article 1(7):for: 7. Article 16 is replaced by the following:Article 16(…) 3.The marketing authorisation holder shall ensure that the product information is kept up to date with the current scientific knowledge including the conclusions of the assessment and recommendations made public by means of the European medicines web-portal established in accordance with Article 26. 4.In order to be able to continuously assess the risk-benefit balance, the Agency may at any time ask the marketing authorisation holder to forward data demonstrating that the risk-benefit balance remains favourable. The marketing authorisation holder shall answer fully and promptly any such request. The Agency may at any time ask the marketing authorisation holder to submit a copy of the pharmacovigilance system master file. The marketing authorisation holder shall submit the copy at the latest 7 days after receipt of the request.;, read: 7. In Article 16, paragraphs 1, 2 and 3 are replaced by the following:Article 16(…) 3.The marketing authorisation holder shall ensure that the product information is kept up to date with the current scientific knowledge including the conclusions of the assessment and recommendations made public by means of the European medicines web-portal established in accordance with Article 26. 3a.In order to be able to continuously assess the risk-benefit balance, the Agency may at any time ask the marketing authorisation holder to forward data demonstrating that the risk-benefit balance remains favourable. The marketing authorisation holder shall answer fully and promptly any such request. The Agency may at any time ask the marketing authorisation holder to submit a copy of the pharmacovigilance system master file. The marketing authorisation holder shall submit the copy at the latest seven days after receipt of the request.;.