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  • Remit

    We contribute to making sure that foodstuffs in Germany are safe. To this end, we co-ordinate control programmes on foodstuffs traded, also on the internet. Further, we authorise plant protection products, veterinary drugs, and genetically modified organisms – provided they are harmless to the health of humans, animals, and the environment. We regularly inform the public about our work, publishing, among other things, yearly reports and data on the quality of foodstuffs in Germany.

      • Prevention
      • Coordinating
      • Authorising
      • Communicating
      • Export affairs
      • G@ZIELT: Safe shopping on the internet
      • International

  • Tasks

    The Federal Office of Consumer Protection and Food Safety (BVL) fulfils many tasks in the area of food safety. The aim of the BVL is to make the communication of risks more transparent and to manage risks before they turn into crises.

      • Food

        Many paths – one goal: Safe food

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      • Feed

        Healthy fed animals – safe food

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      • Consumer products

        Risk management from A to Z

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      • Plant protection products

        Critically examined - plant protection products

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      • Veterinary medicines

        Effective and safe veterinary medicines – healthy animals

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      • Genetic engeneering

        Genetic engineering – check carefully, approve safely

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      • Laboratories

        Analyses at the highest level

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    • Remit  Anzahl der Unterpunkte:  7
      • Prevention 
      • Coordinate 
      • Authorising 
      • Communicating 
      • G@ZIELT: Safe shopping on the internet  
      • Export affairs 
      • International 
        • Cooperation 
          • International support 
            • Twinning 
            • TAIEX 
            • TCF 
        • Projects 
        • Boards 
          • HoA - Heads of Food Safety Agencies 
          • CCNFSDU - Codex Alimentarius Committee on Nutrition and Foods for Special Dietary Uses 
        • BTSF initiative 
          • FAQ - Better Training for Safer Food (BTSF) 
    • Tasks  Anzahl der Unterpunkte:  7
      • Food 
        • Tasks in the field of foodstuffs  
          • Who does what? 
            • Competent ministries and senate administration departments in the federal states 
          • Official food control 
            • Many paths, one goal: Safer food 
            • Multiannual National Control Plan 
            • Federal control plan 
            • National Monitoring 
              • The National Monitoring Programme 2020 
              • Abstract Reports on the National Monitoring, Archive 
                • Abstract Report 2002 
                • Abstract Report 2003 
                • Abstract Report 2004 
                • Abstract Report 2005 
                • Abstract Report 2006 
                • Abstract Report 2007 
                • Abstract Report 2008 
                • Abstract Report 2009 
                • Abstract Report 2010 
                • Abstract Report 2011 
                • Abstract Report 2012 
            • NRCP and ICP for food of animal origin 
            • Zoonoses monitoring 
            • National Report on Residues of Plant Protection Products 
            • Report on irradiated food 
            • Audits and study visits 
            • Data management 
            • ALS 
            • ALTS 
          • Alert and information systems 
            • Alert and information systems 
              • The European Rapid Alert System for Food and Feed (RASFF) 
                • Notifications in the European Rapid Alert System for Food and Feed 
                • Notifications in the rapid alert system from previous years 
              • The European Rapid Alert System for Consumer Products (RAPEX) 
              • The European Network for Administrative Assistance and Cooperation (ACC) 
              • INFOSAN 
              • Food product alerts 
                • FAQs 
              • FIS-VL  
          • Cross-border trade 
          • G@ZIELT: Safe Shopping on the Internet 
          • Joint Commission of Experts on the Classification of Substances 
          • Working Group „Food Supplements” of Heads of Food Safety Agencies 
            • Documents HoA WG FS 
          • Crisis Management  
          • FBO and Zoonoses 
      • Feed 
        • Tasks in the area of feed 
      • Consumer products 
        • Tasks in the area of consumer products 
      • Plant protection products 
        • Tasks in the field of plant protection products 
          • Authorisation of plant protection products 
            • Authorised Plant Protection Products 
              • Online database 
            • Registration reports 
              • Registration reports 
            • Domestic sales and export 
          • EU Review Programme 
            • Legal Regulations for the EU review programme 
            • Information on active substances 
              • Documents on active substances (Germany as RMS) 
            • Assessment procedures 
            • Guidance for applicants 
          • Plant strengtheners 
          • Adjuvants 
          • Task Force "Illegal Trade of Plant Protection Products" 
          • Residues and MRLs 
            • Explanatory Notes on the Regulation on maximum residue levels of pesticides in products of plant and animal origin 
          • Product chemistry 
            • Co-formulants and formulation chemistry 
              • Formulation types 
              • Function of co-formulants 
              • List of unwanted substances in plant protection products 
              • Maximum concentration levels for foreign substances in plant protection products  
            • Active substances 
            • Analytics 
          • Laboratory for formulation chemistry 
        • For applicants 
          • Latest News 
          • Contact 
          • Electronic application 
          • Authorisation procedure for plant protection products 
            • Forms & Templates 
            • Hazardous substance classification and labelling 
              • Hazardous substance classification and labelling 
              • Labelling of plant protection products 
            • Efficacy and use 
            • Product Chemistry 
              • Classification & labelling 
              • Classification & labelling 
              • Applying for and amending packaging for plant protection products 
              • Applying for and amending packaging for plant protection products 
            • Analytical methods for residues 
            • Residues 
            • Toxicology 
            • Environment 
              • Bee protection in the authorization procedure for plant protection products 
              • Tool Input_Decision for selecting the entry parameters for calculations with the FOCUS-PELMO model 
              • Modelling of entries into groundwater – Implementation in Germany of the EFSA Guidance on DegT50 
            • Registration Mark 
          • Approvals for trial purposes 
          • MRL procedure 
            • Setting maximum residue limits for biocides 
          • Parallel trade permits 
            • Application forms and information required 
            • Criteria for approving the parallel trade of plant protection products 
            • Parallel trade - Regulatory framework 
          • EU Review of active substances 
          • Approval of basic substances 
          • Notification of sales and export 
          • Notification procedure for plant strengtheners 
          • Approval procedure for adjuvants 
          • Legal Framework 
            • National Regulations 
            • Regulations in the EU 
            • International Agreements 
              • Code of Conduct on Pesticide Management 
              • Rotterdam Convention 
                • Background information on the Rotterdam Convention 
              • Stockholm Convention 
              • Basel Convention 
              • Vienna Convention / Montreal Protocol to protect the ozone layer 
              • Minamata Convention on Mercury 
        • For users 
          • Proper use 
          • Personal protective equipment 
          • Parallel trade 
        • Technical information 
      • Veterinary medicines 
        • Tasks in the area of veterinary drugs 
          • Who does what? 
            • Responsibilities 
            • Groups and units  
          • Marketing authorisation, registration, exemptions 
            • European marketing authorisation procedures 
              • Centralised procedure 
              • Mutual Recognition Procedure 
              • Decentralised procedure 
            • National authorisation 
            • Veterinary medicinal products for food-producing animals 
            • Assessment of applications for marketing authorisation 
              • Efficacy and target animal safety 
              • User safety 
              • Determination of Withdrawal Periods  
            • Validity of marketing authorisations and re-examination of marketing authorisations for limited markets and in exceptional circumstances 
            • Marketability and legal status of supply 
              • Marketability 
              • Withdrawal 
              • Legal status of supply 
            • Variation of marketing authorisation, registration, exemption 
              • Variations / Changes according to § 4 (4) TAMG 
            • SPC harmonisation 
            • Parallel trade 
            • Registration 
            • Co-distribution of veterinary medicinal products 
            • Examination of registration documents 
          • Residues of vet meds in food 
            • Maximum Residue Limits 
            • Withdrawal periods  
          • Monitoring and risk management 
            • Pharmacovigilance 
            • Adverse event (AE) following the use of a veterinary medicinal product 
            • Signal management 
            • National pharmacovigilance centres 
            • Risk communication 
            • Risk management 
            • Veterinary Medicinal Product Dispensing Volume Register 
              • Mitteilungspflichtige Arzneimittel und Stoffe 
            • PSMF and pharmacovigilance inspections 
            • Post-Marketing Surveillance Studies  
          • Tasks in the area of antibiotic resistance 
            • The recording of antibiotic dispensing quantities 
            • The recording of consumption quantities 
            • The determination of the key figures on therapy frequencies 
              • Bundesweite Kennzahlen der Therapiehäufigkeiten 
            • Instructions for dealing with the Veterinary Home Pharmacy Ordinance 
            • The National Resistance Monitoring of Animal Pathogenic Bacteria (GERM-Vet) 
          • Historical legislation 
            • Renewals 
            • Nachzulassung 
            • PSURs (Periodic Safety Update Reports) 
            • Sunset Clause 
            • Stufenplan 
            • Standard marketing authorisations 
          • Crisis management for veterinary medicinal products at the BVL 
        • For users of veterinary medicinal products 
          • Things to know about veterinary medicinal products 
          • What are adverse events?  
            • General information on adverse events (AE) 
            • What should be reported? 
            • What happens after an adverse event has been reported? 
          • Further information on animal health  
          • Register of online veterinary medicinal products retailers 
            • EU safety logo 
            • How to use register of online veterinary medicine retailers 
            • FAQs register of online retailers 
            • counterfeit 
            • Table register of veterinary medicine online retailers 
          • Disposal of unused veterinary medicines  
          • Frequently Asked Questions (FAQ) - Consumer Enquiries 
        • For veterinarians 
          • Promulgations of the BVL 
            • Tierarzneimittel-Bekanntmachungen 
          • Summary of Product Characteristics (SPC) 
          • Publications and presentations 
            • Archive of Publications 
          • Antibiotic resistance 
            • Antibiotic resistance in general 
            • Antibiotic resistance in pets and hobby animals 
            • Antibiotic resistance in the environment 
            • Antibiotic resistance limitation programmes and measures 
          • Further information on animal health 
        • For applicants and companies 
          • General information 
            • Procedural guidance 
              • Usage of the electronic application form (eAF)  
              • CEP - Certificate of Suitability of Monographs of the European Pharmacopoeia 
              • Guidance on applications  
              • General information and legal basis 
              • Templates for product information texts for veterinary medicinal products 
            • Scientific consultations 
          • Advice on the electronic submission of procedural documents  
            • Electronic submission of documents for applications (eSubmission)  
            • Electronic submission of product literature  
            • Electronic submission of adverse event reports following the use of veterinary medicinal products 
              • Dateneingabe in das nationale Online-Meldeformular für pharmazeutische Unternehmer 
              • Dateneingabe in das Online-Formular der Europäischen Arzneimittel-Agentur 
              • Dateneingabe in das europäische Datenbanksystem 
              • Datenübermittlung aus firmeneigener Datenbank per ESTRI-Gateway in die Datenbanken der zuständigen Bundesoberbehörde 
          • Notification form for veterinary medicinal product shortages 
          • Regulatory flexibility in the context of the COVID-19 pandemic 
          • Brexit 
          • Forms for various procedures in the veterinary field 
          • Costs 
          • Pharmacovigilance obligations and pharmacovigilance information for pharmaceutical companies 
            • Information for representatives of the marketing authorisation holder and co-distributors 
            • Electronic submission of adverse event reports 
          • Further information on veterinary medicinal products 
        • European Regulation on Veterinary Medicinal Products 
          • The objectives of the EU Veterinary Medicinal Products Regulation 
          • Delegated acts, implementing acts and national adaptations 
          • Links und News 
        • Announcements 
      • Genetic engineering 
        • Tasks in the area of genetic engineering 
          • Who does what? 
          • Responsibilities in specific areas 
            • Monitoring 
          • Responsibilities for biosafety institiutions 
            • Cartagena Protocol 
        • For consumers 
          • Handling 
            • Placing on the market of genetically modified organisms 
            • Deliberate release 
            • Transport  
          • Authorization procedures 
            • Authorisation procedure for the placing on the market of GMOs 
            • Authorisation procedure for releases 
          • After authorization 
            • Labelling and traceability 
            • GMO location register  
            • Monitoring 
            • Inspection and control 
          • Detection methods and sampling 
          • Biosafety institutions 
            • Cartagena protocol 
            • Central Committee on Biological Safety 
          • More Information (in German) 
            • Databases 
            • Collection of links 
          • Legal framework  
            • Germany 
            • Europe 
            • Internationally 
        • For applicants and practitioners 
          • Deliberate release 
            • Authorisation procedure 
            • Applying for a release 
            • GMO location register 
          • Placing on the market 
            • Application for placing on the market 
            • Location register 
            • Monitoring 
          • Transport of genetically modified organisms 
          • Genetically modified organisms after authorisation 
            • Labelling and traceability 
            • GMO location register 
            • Monitoring 
            • Inspection 
          • Biosafety Institutions 
            • Central Committee on Biological Safety 
            • Cartagena Protocol 
          • Detection methods and sampling 
          • More Information 
            • Databases 
            • Links 
          • Legal framework 
            • Germany 
            • Europe 
            • International 
        • Announcements 
      • Laboratories 
        • Analytical tasks 
          • Who does what? 
          • Reference laboratories 
            • European Union Reference Laboratory (EURL) 
            • National Reference Laboratories (NRL) 
          • National resistance monitoring 
          • Official Collection of Methods of Analysis 
          • Accreditation and quality assurance 
        • For consumers 
          • Reference laboratories 
          • What is a proficiency test? 
          • Point of contact for consumers 
    • Service  Anzahl der Unterpunkte:  6
      • Media Center 
        • Reports 
        • Video 
        • Flyer 
        • JCF - Scientific Journal 
          • Scientific Advisory Board 
          • Aims and Scope 
      • Press 
        • Contact for journalists 
        • Press Events 
        • Press reports 
        • Press mailing list 
        • JCF - Scientific Journal 
          • Scientific Advisory Board 
          • Aims and Scope 
      • Events 
        • Start 
          • Programme & Presentations 
          • Venue / Contact 
          • Livestream 
        • Event archive 
      • Questions and Answers 
        • FAQs for consumers 
          • FAQ for consumers on veterinary medicinal products (vmp) 
        • FAQ for companies, producers and applicants 
          • FAQ Veterinary Medicines 
      • Newsletter 
      • Contact 
    • The Federal Office  Anzahl der Unterpunkte:  4
      • Core Mission 
      • Structure 
      • History of the BVL 
      • Directions and Adresses 
        • Braunschweig Bundesallee 
        • Berlin Gerichtstraße 
    • Announcements  Anzahl der Unterpunkte:  6
      • Announcements 'Safe Food' 
      • Announcements 'Consumer products' 
      • Announcements 'Plant protection products' 
      • Announcements 'Veterinary drugs' 
      • Announcements 'genetic engineering' 
      • Announcements 'Laboratories' 

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Information for veterinarians

Here, veterinarians can find up-to-date information, for example on the marketing authorisation, registration and marketability of veterinary medicinal products, publications, explanations and comments on various topics of animal welfare and animal health.

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  2. Tasks
  3. Veterinary medicines
  4. For veterinarians
  5. Promulgations of the BVL
  6. Tierarzneimittel-Bekanntmachungen

Bekanntmachungen

Search results 1 to 10 from a total of 140

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Date Title
15.11.2018 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 23. Oktober 2018
11.09.2018 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 24. August 2018
11.10.2018 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 25. September 2018
28.09.2018 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 28. September 2018
29.03.2018 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 29. März 2018
29.03.2019 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 29. März 2019
30.09.2019 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 30. September 2019
31.03.2020 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 30. September 2020
31.03.2020 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 31. März 2020
31.03.2015 Bekanntmachung der Therapiehäufigkeit im Bundesanzeiger vom 6. März 2015
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