Robuta

https://www.jnj.com/media-center/press-releases/janssen-submits-european-marketing-authorisation-application-for-canagliflozin-in-type-2-diabetes Janssen Submits European Marketing Authorisation Application for Canagliflozin in Type 2 Diabetes marketing authorisation https://www.gov.uk/government/collections/transfer-ownership-of-a-marketing-authorisation Transfer ownership of a marketing authorisation for medicines - GOV.UK How to transfer the ownership of a marketing authorisation including the form you need to complete. transfer ownershipmarketing authorisationmedicinesuk https://www.gsk.com/en-gb/media/press-releases/european-medicines-agency-accepts-marketing-authorisation-application-for-momelotinib-for-the-treatment-of-myelofibrosis/ European Medicines Agency accepts marketing authorisation application for momelotinib for the... Application includes data from key phase III trials, including the pivotal MOMENTUM trial. european medicines agencymarketing authorisationacceptsapplication https://www.gsk.com/en-gb/media/press-releases/glaxosmithkline-submits-european-marketing-authorisation-application-for-pazopanib-in-advanced-kidney-cancer/ GlaxoSmithKline submits European marketing authorisation application for Pazopanib in advanced... GSK announced submission of MAA to EMEA for pazopanib, oral therapy for metastatic renal cell carcinoma (RCC). marketing authorisationglaxosmithklinesubmitseuropeanapplication https://www.biospace.com/averoa-submits-marketing-authorisation-application-to-the-european-medicines-agency-seeking-approval-of-ava1014-for-treating-complications-associated-with-chronic-kidney-disease AVEROA Submits Marketing Authorisation Application to the European Medicines Agency Seeking... Apr 24, 2024 - Averoa announces the submission of a marketing authorisation application to the European Medicines Agency for Ferric Citrate Coordination Complex, an oral... european medicines agencymarketing authorisationto thesubmitsapplication https://www.gsk.com/en-gb/media/press-releases/european-medicines-agency-ema-accepts-marketing-authorisation-application-for-daprodustat/ European Medicines Agency (EMA) accepts marketing authorisation application for daprodustat | GSK The EMA has validated the MAA for daprodustat, for the treatment of patients with anaemia of chronic kidney disease. european medicines agencymarketing authorisationemaaccepts https://investingnews.com/eisai-and-nuvation-bio-announce-marketing-authorisation-application-for-taletrectinib-for-the-treatment-of-advanced-ros1-positive-non-small-cell-lung-cancer-validated-by-the-european-medicines-agency/ Eisai and Nuvation Bio Announce Marketing Authorisation Application for Taletrectinib for the... Mar 26, 2026 - The Marketing Authorisation Application (MAA) has been validated and accepted for full approval consideration with a standard review timelineAdditional filings... marketing authorisationeisaibioannounce https://www.esmo.org/oncology-news/ema-recommends-granting-a-marketing-authorisation-for-lurbinectedin EMA Recommends Granting a Marketing Authorisation for Lurbinectedin | ESMO marketing authorisationemarecommendsgrantingesmo https://www.gsk.com/en-gb/media/press-releases/viiv-healthcare-receives-eu-marketing-authorisation-for-the-first-ever-dispersible-tablet-formulation-of-dolutegravir-tivicay-a-treatment-for-children-living-with-hiv-in-europe/ ViiV Healthcare receives EU Marketing Authorisation for the first-ever dispersible-tablet... The EU Marketing Authorisation follows the US Food and Drug Administration (FDA) approval of Tivicay PD in 2020. viiv healthcaremarketing authorisation https://www.gov.uk/government/publications/medicines-marketing-authorisation-change-of-ownership-application Medicines marketing authorisation: change of ownership application - GOV.UK Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner. change of ownershipmarketing authorisationmedicinesapplicationuk https://www.gov.uk/guidance/apply-to-change-a-veterinary-marketing-authorisation-or-homeopathic-remedy Apply to change a veterinary Marketing Authorisation or Homeopathic Remedy - GOV.UK Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy. apply toveterinary marketing https://www.jnj.com/media-center/press-releases/janssen-submits-marketing-authorisation-application-to-the-european-medicines-agency-seeking-approval-of-lazertinib-in-combination-with-rybrevant-amivantamab-for-the-first-line-treatment-of-patients-with-egfr-mutated-non-small-cell-lung-cancer Janssen Submits Marketing Authorisation Application to the European Medicines Agency Seeking... Nov 30, 2025 - The submission is supported by data from the Phase 3 MARIPOSA study, which featured in a Late-Breaking Presidential Symposium session at the 2023 ESMO... european medicines agencymarketing authorisationto thejanssensubmits https://www.jnj.com/media-center/press-releases/janssen-submits-marketing-authorisationapplication-to-the-european-medicines-agency-seeking-approval-of-erdafitinib-for-the-treatment-of-patients-with-locallyadvanced-or-metastatic-urothelial-cancer-with-susceptible-fgfr-alterations Janssen Submits Marketing Authorisation Application to the European Medicines Agency Seeking... Nov 30, 2025 - Pending approval, erdafitinib, an investigational, once-daily oral pan-fibroblast growth factor receptor (FGFR) tyrosine kinase inhibitor,1will become the... european medicines agencymarketing authorisationto thejanssensubmits https://www.prnewswire.co.uk/news-releases/thrombogenics-announces-ema-acceptance-for-review-of-marketing-authorisation-application-for-ocriplasmin-144765755.html ThromboGenics Announces EMA Acceptance for Review of Marketing Authorisation Application for... /PRNewswire/ -- If Approved, Ocriplasmin Will be the First Pharmacological Treatment for Symptomatic Vitreomacular Adhesion (VMA) Including Macular Hole... for reviewmarketing authorisationannouncesemaacceptance https://www.esmo.org/oncology-news/ema-recommends-granting-a-marketing-authorisation-for-tarlatamab EMA Recommends Granting a Marketing Authorisation for Tarlatamab | ESMO marketing authorisationemarecommendsgrantingesmo