Official announcements
Recall
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Medicines
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11/03/2019
The marketing authorisation holder informed its customers on March 6, 2019 that the marketing of „Tetraspan 60 mg/ml Infusionslösung“ and „Venofundin 60 mg/ml Infusionslösung“ is ceased permanently for economic reasons.
Recall
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Medicines
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21/02/2019
The marketing authorisation holder informed its customers on February 19, 2019 that the marketing authorisation of „Vantobra 170 mg Lösung für einen Vernebler“ will be withdrawn.
messages in brief
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21/02/2019
For more information on this topic, follow the link to the security features .
Recall
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Medicines
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15/02/2019
The parallel distributor „HAEMATO PHARM GmbH“ informed its customers on February 14, 2019 that the supply chain is not fully documented and GDP-guidelines are not met.
Enforcement
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15/02/2019
Special occasions should be celebrated appropriately: For some this means letting themselves go for a change, if necessary by taking various substances. However, not everyone wants to break the law and so you may come across products that are offered as a legal alternatives to other party drugs. At the same time, it is suggested by the suppliers that such products are completely harmless. Does "not prohibited" mean the same as "legal" and is this synonymous with "risk-free"?
Safety warnings
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messages in brief
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14/02/2019
During the transitional phase, strict limits are already in place for these impurities.
Safety warnings
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Medicines
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14/02/2019
During the transitional phase, strict limits are already in place for these impurities.
messages in brief
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04/02/2019
The National Immunization Schedule 2019 ("Österreichischer Impfplan") is now available. link: https://www.sozialministerium.at/site/Gesundheit/Krankheiten_und_Impfen/Impfen/Oesterreichischer_Impfplan_2019
messages in brief
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04/02/2019
In December 2018 the Committee for Medicinal Products for Veterinary Use (CVMP) adopted a guideline on the assessment and control of DNA reactive (mutagenic) impurities in veterinary medicinal products. The calculated threshold values are intended to…
messages in brief
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04/02/2019
The EMA published a revision of the “Guideline on the environmental risk assessment (ERA) of human medicines” on 30 November 2018. The guideline is now open for public consultation until 30 June 2019. The purpose of the ‚Guideline on Environmental…