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Les médicaments vétérinaires en Europe

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EFSA 24/03/21 Résidus de médicaments vétérinaires : des taux de conformité toujours élevés. EFSA 24/03/21 Report for 2019 on the results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products. EUROPEAN MEDICINES AGENCY 21/01/21 Veterinary medicines: highlights of 2020. NUFFIELDSCHOLAR - DEC 2020 - Animal Medicine Best Practice: unlocking the potential for UK farming. Environmental Sciences Europe 20/07/20 Regulatory review of the environmental risk assessment of veterinary medicinal products in the European Union, with particular focus on the centralised authorisation procedure. The environmental risk assessment for veterinary pharmaceutical products Since 2005, in the EU, the assessment of environmental risks of veterinary pharmaceuticals has been done following the approach outlined in VICH guidelines 6 and 38.

Environmental Sciences Europe 20/07/20 Regulatory review of the environmental risk assessment of veterinary medicinal products in the European Union, with particular focus on the centralised authorisation procedure

The risk assessment is tier-based and consists of two phases. The first phase, or Phase I (outlined in VICH guideline 6), is focused on determining the environmental exposure to the veterinary medicinal product, and concludes on whether or not a higher ecotoxicological assessment is needed, depending on the extent of environmental release as a result of the use of the product only (i.e., other product lifecycle stages such as manufacturing and disposal are excluded from exposure considerations). In limited cases, however, a Phase II assessment might be needed for any product that would otherwise stop in Phase I. If the conclusion of a Phase I environmental risk assessment is that environmental exposure is not low (e.g. EUROPEAN MEDICINES AGENCY 13/03/20 WITHDRAWAL OF THE UNITED KINGDOM AND EU RULES FOR MEDICINAL PRODUCTS FOR HUMAN USE AND VETERINARY MEDICINAL PRODUCTS. MOLECULES 17/12/19 Advances in the Analysis of Veterinary Drug Residues in Food Matrices by Capillary Electrophoresis Techniques.

The addition of drugs (abuse or illegal use) to animal food to promote growth and protect animals can represent a potential risk of contamination of food matrices.

MOLECULES 17/12/19 Advances in the Analysis of Veterinary Drug Residues in Food Matrices by Capillary Electrophoresis Techniques

Drugs, such as antibiotics, estrogens, non-steroidal anti-inflammatory drugs (NSAIDs), and β-agonists, which are usually used in feedstuffs, can contaminate different food products, mainly meat, milk, and dairy products, causing health problems and also serious diseases [1]. In particular, the abuse of antibiotics in food-producing animals, which contributes to the increase in risk of the transfer of antibiotic resistance from animals to humans, is a very important issue for human health.

For this reason, the European Union (EU) and the Food and Drug Administration (FDA) established restrictive regulations for the control of pharmacologically active substance residues and fixed maximum residue limits (MRLs) in edible animal tissues to preserve foodstuff of animal origin and consumers [2,3,4]. EFSA 31/03/20 Report for 2018 on the results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products.

PARLEMENT EUROPEEN - Réponse à question E-003880/2019 Contingent tarifaire pour les importations de viande bovine américaine et règlement (UE) 2019/6 relatif aux médicaments vétérinaires. Salute_gov_it 22/10/19 TRAD AUTO : La direction générale de la santé animale et des médicaments vétérinaires a mis en place une application Web pour la publication des dispositions relatives aux médicaments vétérinaires sur le site Web du ministère de la. La Direzione generale della sanità animale e dei farmaci veterinari ha implementato un applicativo web per la pubblicazione dei provvedimenti relativi ai medicinali veterinari sul sito istituzionale del Ministero della Salute.

salute_gov_it 22/10/19 TRAD AUTO : La direction générale de la santé animale et des médicaments vétérinaires a mis en place une application Web pour la publication des dispositions relatives aux médicaments vétérinaires sur le site Web du ministère de la

La nuova modalità, che sostituisce la pubblicazione tradizionale nella Gazzetta Ufficiale della Repubblica Italiana, si inserisce nell’ottica della semplificazione amministrativa prevista dall’articolo 32 della legge n. 69/2009. Dal 1° novembre 2019 i seguenti provvedimenti: decreti di autorizzazione all’immissione in commercio (nuove autorizzazioni, importazioni parallele) decreti di revoche e sospensione dell’autorizzazione all’immissione in commercio provvedimenti relativi alle variazioni dei termini dell’autorizzazione all’immissione in commercio saranno pubblicati sul sito istituzionale del Ministero della Salute, con funzione di pubblicità legale e non saranno più disponibili sulla Gazzetta Ufficiale della Repubblica Italiana.

Consulta. EFSA 13/05/19 Résidus de médicaments vétérinaires : les taux de conformité restent élevés. Les données de surveillance sur la présence de résidus de médicaments vétérinaires et de contaminants chez les animaux et dans les aliments d'origine animale montrent des taux élevés de conformité avec les niveaux de sécurité recommandés.

EFSA 13/05/19 Résidus de médicaments vétérinaires : les taux de conformité restent élevés

La présence de substances interdites est également faible. Le pourcentage d'échantillons dépassant les limites maximales était de 0,35% pour l'année 2017. Ce chiffre se situe dans l’intervalle compris entre 0,25% et 0,37% observé au cours de ces dix dernières années. La non-conformité en ce qui concerne certains contaminants chimiques tels que les métaux s’est révélée plus élevée que pour les autres groupes de substances ; le cadmium, le plomb, le mercure et le cuivre étant les contaminants les plus fréquemment identifiés.

C’est la première fois que l’EFSA recueille ces données auprès des États membres ; dans le passé, ces informations étaient transmises directement à la Commission européenne. GOV_UK 24/09/18 Registration of veterinary medicines if there’s no Brexit deal. GOV_UK 24/09/18 Regulation of veterinary medicines if there’s no Brexit deal. JOUE 30/05/18 RÈGLEMENT (UE) 2018/782 DE LA COMMISSION du 29 mai 2018 établissant les principes méthodologiques applicables à l'évaluation du risque et aux recommandations pour la gestion du risque visés dans le règlement (CE) n° 470/2009. EFSA 30/11/17 Résidus de médicaments vétérinaires en 2015 : les chiffres restent stables.

EMA 10/05/17 European Medicines Agency’s (EMA) 2016 annual report. EMA 2016 annual report published The European Medicines Agency’s (EMA) 2016 annual report published today focuses on the Agency’s key achievements in the areas of medicine evaluation, support to research and development of new and innovative treatments and the safety monitoring of medicines in real life.

EMA 10/05/17 European Medicines Agency’s (EMA) 2016 annual report

In 2016, the Agency recommended a marketing authorisation for 81 medicines for human use, including 27 new active substances. Many of these innovative substances build on the advances made in biomedical science and have the potential to make a difference for patients. On the veterinary side, 11 medicines were recommended for approval, including six new active substances. A third of these medicines prevent viral or bacterial infections in food-producing animals. Approximately half of the applicants who were granted a positive opinion for their medicine had received scientific advice from EMA during the development phase of their product. PARLEMENT EUROPEEN - Réponse à question E-005882-16 Marketing authorisation for veterinary drugs.

EMA - MAI 2016 - Committee for Medicinal Products for Veterinary Use - Reflection paper on non-spontaneous adverse event reports (peer-reviewed literature, internet and social media) RIKILT - WAGENINGEN - 2012 - Veterinary drugs and growth promoting agents in animal products - Annual report 2012. AFSCA - JUILLET 2013 - LABINFO - Au sommaire: Contrôle de la qualité des réactifs vétérinaires (ELISA et PCR en temps réel) destinés aux laboratoires de diagnostic.

DEFRA VMD - Veterinary Medicines Directorate - Annual Report & Accounts 2013/14. EFSA 18/11/15 Veterinary drug residue data for 2013 stable. PARLEMENT EUROPEEN - Réponse à question P-010707-15 Veterinary medicinal product concerns. EFSA 31/03/15 Sample-based data model extended to veterinary drug residues. Nouvelle31 mars 2015 EFSA is extending the use of its harmonised sample-based data reporting model to the collection of data on veterinary medicinal product residues in animals and animal products.

EFSA 31/03/15 Sample-based data model extended to veterinary drug residues

Sample-based reporting using standardised description elements is already used to collect occurrence data from Member States in areas such as food additives, chemical contaminants, pesticide residues and antimicrobial resistance. Monitoring data on veterinary medicinal product (VMP) residues are currently submitted annually in an aggregated format to a database maintained by the European Commission. EFSA then examines the data and presents the results in annual reports. However, aggregation does not lend itself to complex statistical analysis and is of limited value for quantitative exposure and risk assessments. As with the other areas, providers will be asked to submit data through EFSA’s web-based Data Collection Framework (DCF). 2012 - Les médicaments dans l’exploitation agricole - vade-mecum pour l'éleveur.

Les médicaments vétérinaires en France

CONFFIDENCE 16/05/12 CONffIDENCE cluster workshop - Work Packages 2a & 2b: Detection, analysis and control of veterinary pharmac. Detection, analysis and control of veterinary pharmaceuticals in food and feed. 16 May 2012 In the frame of the FP7 CONffIDENCE (CONtaminants in Food and Feed: Inexpensive DetectioN for Control of Exposure) project, a half day workshop entitled "Detection, analysis and control of veterinary pharmaceuticals in food and feed" was held following the EURORESIDUE VII Conference, at Hotel Zuiderduin, Egmond aan Zee, the Netherlands.

CONFFIDENCE 16/05/12 CONffIDENCE cluster workshop - Work Packages 2a & 2b: Detection, analysis and control of veterinary pharmac

During the CONffIDENCE workshop, results were presented through 3 lectures, 5 posters and demonstration activities. Opportunities for discussions on the presented project activities with stakeholders were available. Approximately 20 participants attended to the workshop. Programme CONffIDENCE Cluster 2 workshop. CONFEDERATION SUISSE 07/09/10 Baisse des quantités d’antibiotiques vendues en médecine vétérinaire en 2009 par rapport aux année. Les antibiotiques les plus vendus en Suisse sont les sulfamidés (42 %), suivis par les tétracyclines (23 %) et les pénicillines (19 %).

CONFEDERATION SUISSE 07/09/10 Baisse des quantités d’antibiotiques vendues en médecine vétérinaire en 2009 par rapport aux année

Quant à la baisse de la quantité totale d’antibiotiques vendus l’année dernière, elle s’explique essentiellement par le recul des tétracyclines (-1140 kg) et des pénicillines (-715 kg). Si l’on met en regard ces quantités vendues et la population d’animaux de rente concernée, on s’aperçoit que la quantité de principes actifs antimicrobiens vendus en Suisse (70 789 kg) se situe dans la moyenne européenne (env. 90 mg/kg). Ainsi, les quantités d’antibiotiques utilisées étaient similaires en Allemagne et inférieures dans les pays scandinaves, mais bien supérieures en France et aux Pays-Bas. Les mammites sont une affection fréquente en médecine vétérinaire.

Ainsi, 5190 kg de principes actifs ont été vendus dans des préparations administrées aux vaches par voie intra-mammaire. THESE DE L'ECOLE VETERINAIRE DE LYON - 2008 - La réglementation européenne du médicament vétérinaire. JOUE 22/01/10 Communication de la Commission — Lignes directrices concernant les caractéristiques des différentes catégories de. CIRAD/AQUATROP 19/03/09 La législation française et européenne sur les résidus et les substances médicamenteuses chez le poisson.

EUDRALEX - Volume 5 - Pharmaceutical legislation : Veterinary Medicinal Products. France 2005-7506 Control of residues and contaminants in live animals and animal products, including controls on veterinary medi. DG SANCO 08/09/10 food safety - Food and Veterinary Office - Inspection reportsFR France - Control of residues and contaminan. EUROPE 19/02/03 Questions et réponses concernant les résidus et les contaminants dans les denrées alimentaires.

EUROPE - Résidus de médicaments vétérinaires dans les aliments d'origine animale. Archives Règlement (CEE) n° 2377/90 du Conseil du 26 juin 1990 établissant une procédure communautaire pour la fixation des limites maximales de résidus de médicaments vétérinaires dans les aliments d'origine animale [Voir actes modificatifs].

EUROPE - Résidus de médicaments vétérinaires dans les aliments d'origine animale

En raison de l'incidence que peuvent avoir les substances contenues dans les médicaments vétérinaires destinés à des animaux producteurs d'aliments, le présent règlement classifie ces substances. EUROPE - Médicaments vétérinaires. Food Safety - Chemical Safety of Food - Residues of Veterinary Medicinal Products - Community Reference Laboratories. Requires javascript EU Reference Laboratories The EU's network of laboratories for the control of residues includes: EU Reference Laboratories (EU-RLs) designated by the Commission; National Reference Laboratories (NRLs) designated by each EU-countries; Official control laboratories under the responsibility of EU-countries.

Food Safety - Chemical Safety of Food - Residues of Veterinary Medicinal Products - Community Reference Laboratories

EU and national reference laboratories contribute to high quality and uniformity of analytical results. Food Safety - Chemical Safety of Food - Residues of Veterinary Medicinal Products - Community Reference Laboratories. Ema.europa. REGLEMENT (CE) N° 470/2009 DU PARLEMENT EUROPEEN ET DU CONSEIL du 6 mai 2009 établissant des procédures communautaires pour la f.