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Round table on "Availability of medicines in Austria" (2)

messages in brief | 21/10/2019
The second round table discussing the availability of medicines in Austria took place on October 15, 2019.
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News

Review of ranitidine-containing drugs due to possible contamination with NDMA.

Safety warnings | messages in brief | 17/09/2019

Measures at EU level

At the request of the European Commission, the European Medicines Agency (EMA) has begun reviewing medicines containing…

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News

Supply bottleneck Imurek

messages in brief | 26/07/2019

Situation in Austria

Imurek-50 mg Film-Coated Tablets are currently temporarily unavailable due to increased demand beyond national borders, and…

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News

Accessible patient information leaflet

messages in brief | 18/07/2019
Please find new and updated FAQ's regarding "Accessible Patient Information Leaflet" at https://www.basg.gv.at/en/medicines/faqs-about-medicinal-pro…
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News

Time savings due to parallel submissions in batch release

messages in brief | 18/07/2019
The concept of parallel submission in official control authority batch release means that the applicant sends samples to the BASG-OMCL (Official…
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News

Medical devices: New information on implant card and person responsible for regulatory compliance

messages in brief | 17/07/2019
  • Manufacturers of an implantable device shall provide information for identification of the device on an implant card in accordance with Article 18…
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News

The authorisation status of allergen products

messages in brief | 10/05/2019
The authorisation status of allergen products, both for diagnosis and therapy, in the European Union is heterogeneous.
In order to facilitate…
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News

Update Community Referral Sartans

messages in brief | 07/05/2019
The Commission Implementing Decision is published. Further information can be found under:  https://www.basg.gv.at/de/news-center/news/news-detai…
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News

Medical devices: Information on consultation procedures, registration of guideline products and registration deadlines published

messages in brief | 24/04/2019

Article 54 of the MDR regulates the consultation procedure related to the clinical evaluation of certain class III and class IIb devices. Regarding…

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