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65 (3) of the Austrian Medicines Act via electronic submission in the eService (https://eservices.basg.gv.at/ ). The following key personnel are not subject to notification : - Head of Production: requirements [...] responsible person according to § 9 (4) GSG via electronic submission in the eService (https://eservices.basg.gv.at/ ) are subject to notification in advance or without undue delay in case of unforeseen changes [...] undue delay in case of unforeseen changes via electronic submission in the eService (https://eservices.basg.gv.at/) . e. Licence holder: Pursuant to § 56 (2) of the Austrian Medicines Act (AMG ) as amended
certification documents and the final report are sent to the Federal Office for Safety in Health Care (BASG). The procedure has now been completed ( AVG ). Electronic submission The in the following listed
clinical trials Interventional clinical trials must be approved by both the regulatory authority (BASG) and the ethics committees. The submission documents consist of the following three parts: information
Referrals and PSUSAs will be published on the BASG homepage ( PV-wordings ) When submitting the variation, please state the following in accordance with the BASG letter in the coverletter ( e.g. ' PHV-Issue:
medicinal products) and send it to BASG if an import certificate or a certificate of marketability according to the Medicinal Products Import Act (AWEG) is to be applied for at BASG. Note: If, in the case of [...] notification for the study medication has to be sent to the Federal Office for Safety in Health Care (BASG) in any case. For this purpose, please use the electronic reporting portal to be used since 04.07 [...] Notifications (Electronic Submission Ordinance 2011 - EEVO 2011; published in the Official Gazette of the BASG ), applications and notifications under the AWEG have to be submitted in electronic form since 04
current supply situation of certain radiopharmaceuticals, the Federal Office for Safety in Health Care (BASG)/AGES PharmMed draws attention to particularities in the use of unauthorised medicinal products,
für Amtsärzte Zum Gebrauch für die Organe der Bezirksverwaltungsbehörde - Zur Verfügung gestellt von BASG / AGES OMCL Probenziehung gem. §70 ABO, BGBl. II Nr. 65/2005 (jeweils i.d.g.F.) Formular: Probenb
BASG and companies News Information The new Veterinary Medicinal Products Regulation is to be applied as of 28.01.2022, further information can be found here: The new Veterinary Medicinal Products Regulation [...] is to be applied as of 28.01.2022, further information can be found here: read more Reporting to BASG The Federal Office relies on reports from consumers, health care professionals and companies for the [...] continuous re-evaluation of the safety profile of medicinal products and medical devices. Reporting to BASG read more BREXIT The transition period ended on 31.12.2020. Marketing authorisation holders are reminded
the BASG, this provision must be interpreted as meaning that the marketing authorisation holder must be informed at the latest at the same time as the application; from the point of view of the BASG, there [...] or can the tray be labelled with the information required for the primary container? 14. How is the BASG to be informed about the products we display at the EMA? 15. In case of nat. approved preparations [...] authorisation,applicant shall be informed of application.Can the appl. be filed earlier? 16. Does the BASG also require a notification to this effect for centrally authorised products? 17. Is a translation
with the involvement of the Ministry of Health and the Federal Office for Safety in Health Care (BASG). The Supervisory and Control Advisory Board of AMVO exercises the supervisory and control powers [...] medicinal products an email with subject „application for § 3a AMBO 2009“ should be forwarded to cp@basg.gv.at . identifyer sticker | 48 KB 12/02/2019