https://www.noahcompendium.co.uk/?id=-470706
Marketing Authorisation Number - Eprizero 5 mg/ml Pour-On Solution for Beef and Dairy Cattle
marketing authorisationsolution fordairy cattlenumbermg
https://www.jnj.com/media-center/press-releases/new-marketing-authorisation-application-submitted-to-ema-for-ibrutinib-for-the-treatment-of-two-forms-of-blood-cancer
New Marketing Authorisation Application Submitted to EMA for Ibrutinib for the Treatment of Two...
Jul 17, 2025 - The submission is for chronic lymphocytic leukemia (CLL)/small lymphocytic leukemia (SLL) and mantle cell lymphoma (MCL), two difficult-to-treat diseases
marketing authorisationthe treatmentnewapplicationsubmitted
https://ogkologos.com/ema-recommends-granting-a-marketing-authorisation-for-zanubrutinib-for-the-treatment-of-waldenstroms-macroglobulinaemia/
EMA Recommends Granting a Marketing Authorisation for Zanubrutinib for the Treatment of...
marketing authorisationthe treatmentemarecommendsgranting
https://ipi.academy/product/details/1701/clinical-overview-and-clinical-summary-creating-effective-marketing-authorisation-applications?fromproduct=2133
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications...
clinical overviewmarketing authorisationsummarycreatingeffective
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 authorisationglaxosmithklineeuropeanapplicationadvanced
https://www.stallergenesgreer.com/press-releases/stallergenes-greer-submits-marketing-authorisation-application-europe-its-sublingual
Stallergenes Greer Submits a Marketing Authorisation Application in Europe for Its Sublingual House...
marketing authorisationgreerapplicationeuropesublingual
https://www.firmenpresse.de/pressrelease17246/dgap-news-sanochemia-pharmazeutika-ag-european-marketing-authorisation-for-mrt-imaging-agent.html
DGAP-News: Sanochemia Pharmazeutika AG: European Marketing Authorisation for MRT Imaging Agent
Sanochemia Pharmazeutika AG / Regulatory Approval10.03.2010 08:40 Dissemination of a Corporate News, transmitted byDGAP - a company of EquityStor ...
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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.
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https://www.famhp.be/en/news/news_rosiglitazone_2010_09_23
Rosiglitazone: EMA recommends suspending the marketing authorisation of Avandia, Avandamet and...
As announced in our press release dated 22/07/2010, the findings of the evaluation of all data on the benefit / risk balance for rosiglitazone-containing...
marketing authorisationemarecommendssuspendingavandia
https://www.advarra.com/learn/clinical-trials-acronyms/marketing-authorisation-application/
Marketing Authorisation Application (MAA) - Clinical Trials Acronym | Advarra
Mar 11, 2026 - A Marketing Authorisation Application (MAA) is the regulatory submission used to request approval to market a medicinal product in the European Union and other...
marketing authorisationclinical trialsapplicationmaaacronym
https://irishpharmacynews.ie/viiv-healthcare-announces-the-marketing-authorisation-of-the-first-complete-long-acting-injectable-hiv-treatment-in-europe/
ViiV Healthcare announces the Marketing Authorisation of the first complete long-acting injectable...
Jan 22, 2021 - ViiV Healthcare announces the Marketing Authorisation of the first complete long-acting injectable HIV treatment in Europe Marketing Authorisation granted by...
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https://ganado.com/european-court-of-justice-provides-clarity-on-the-marketing-authorisation-requirements-of-medicinal-products/
European Court of Justice provides clarity on the marketing authorisation requirements of medicinal...
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https://uk.marketscreener.com/news/savara-inc-announces-mhra-accepts-molbreevi-marketing-authorisation-application-for-autoimmune-pap-ce7e50dad98af02c
Savara Inc. Announces MHRA Accepts Molbreevi Marketing Authorisation Application for Autoimmune PAP...
Apr 7, 2026 - Savara Inc. announced that the MHRA has accepted the submission of the MOLBREEVI MAA for the treatment of autoimmune PAP in the U.K. The MAA was accepted under...
marketing authorisationincannouncesmhraaccepts
https://laegemiddelstyrelsen.dk/en/licensing/licensing-of-medicines/variations/temporary-repackaging-of-medicines-with-a-marketing-authorisation/
Temporary repackaging of medicines with a marketing authorisation
Occasionally, a marketing authorisation holder (MA holder) will need to repackage a medicinal product for a short temporary period. The Danish Medicines Agency...
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https://www.infarmed.pt/web/infarmed-en/human-medicines/marketing-authorisation
Marketing authorisation - INFARMED, I.P.
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https://www.certifico.com/news/ema-recommends-conditional-marketing-authorisation-for-paxlovid
EMA recommends conditional marketing authorisation for Paxlovid
EMA recommends conditional marketing authorisation for Paxlovid
marketing authorisationemarecommendsconditionalpaxlovid
https://elbiruniblogspotcom.blogspot.com/2013/04/orphan-drug-lastest-designations-and_30.html
CIENCIASMEDICASNEWS: Orphan drug lastest designations and marketing authorisation
Orphan drug lastest designations and marketing authorisation About EURORDIS...
marketing authorisationorphandruglastestdesignations
https://www.mundipharma.com/European-Medicines-Agency-accepts-rezafungin-marketing-authorisation-application-for-the-treatment-of-invasive-candidiasis
European Medicines Agency accepts rezafungin marketing authorisation application for the treatment...
European Medicines Agency accepts rezafungin marketing authorisation application for the treatment of invasive candidiasis
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https://www.indianpharmapost.com/news/astrazeneca-pharma-india-surrenders-marketing-authorisation-for-olaparib-100mg-and-150mg-17028
AstraZeneca Pharma India surrenders marketing authorisation for Olaparib 100mg and 150mg
The discontinuation decision is only on the basis of commercial reasons and is not due to efficacy or safety reasons
marketing authorisationastrazenecapharmaindiasurrenders
https://www.amgen.com/newsroom/press-releases/2008/11/nplatetm-romiplostim-receives-positive-opinion-for-marketing-authorisation-in-the-european-union
Nplate(TM) (Romiplostim) Receives Positive Opinion for Marketing Authorisation in the European...
for marketingthe europeannplatetmreceives
https://www.halmed.hr/en/Novosti-i-edukacije/Novosti/2025/Information-to-marketing-authorisation-holders-regarding-variation-applications-after-referral-for-medicinal-products-which-contain-the-active-substance-finasteride-or-dutasteride/3558
Information to marketing authorisation holders regarding variation applications after referral for...
Website provides publications, reports and news regarding the safe use of medicinal products, medical devices and homeopathic medicinal products, as well as...
marketing authorisationafter referralinformationholdersregarding
https://www.eurogct.org/research-pathways/commercialisation/market-access-atmps/expediting-marketing-authorisation-0
Conditional Marketing Authorisation of ATMPs | EuroGCT
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https://salesandmarketingnetwork.com/news_release_bs.html?pipe=0000ac177000191&ID=2028574&key=Salvacyl
News for Medical Sales Reps: Swissmedic Grants Debiopharm Marketing Authorisation for Moapar(R), a...
for medicalsales repsmarketing authorisationnewsswissmedic
https://www.basg.gv.at/en/companies/marketing-authorisation-life-cycle/faq-marketing-authorisation-life-cycle/renewal-of-marketing-authorisation
Renewal of marketing authorisation - BASG
marketing authorisationrenewal