Find research datasets worth reusing

opencc-by-4.0Feb 2022View details →

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Bulgaria

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Bulgaria. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005.  Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – Central Laboratory for Veterinary Sanitary Expertise and Ecology within the Bulgarian Food Safety Agency VMPR_2022 – Central Laboratory for Veterinary Sanitary Expertise and Ecology within the Bulgarian Food Safety Agency VMPR_2021 – Central Laboratory for Veterinary Sanitary Expertise and Ecology within the Bulgarian Food Safety Agency VMPR_2020 – Central Laboratory for Veterinary Sanitary Expertise and Ecology within the Bulgarian Food Safety Agency VMPR_2019 – Risk Assessment Center on Food Chain VMPR_2018 – Bulgarian Food Safety Agency VMPR_2017 – Bulgarian Food Safety Agency

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Hungary

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Hungary. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005.  Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – National Food Chain Safety Office VMPR_2022 – National Food Chain Safety Office VMPR_2021 – National Food Chain Safety Office VMPR_2020 – National Food Chain Safety Office VMPR_2019 – National Food Chain Safety Office VMPR_2018 – National Food Chain Safety Office VMPR_2017 – National Food Chain Safety Office

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Sweden

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Sweden. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005.  Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – National Food Agency VMPR_2022 – National Food Agency VMPR_2021 – National Food Agency VMPR_2020 – National Food Agency VMPR_2019 – National Food Agency VMPR_2018 – National Food Agency VMPR_2017 – National Food Agency

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Lithuania

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Lithuania. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005.  Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – National Food and Veterinary Risk Assessment Institute VMPR_2022 – National Food and Veterinary Risk Assessment Institute VMPR_2021 – National Food and Veterinary Risk Assessment Institute VMPR_2020 – National Food and Veterinary Risk Assessment Institute VMPR_2019 – National Food and Veterinary Risk Assessment Institute VMPR_2018 – National Food and Veterinary Risk Assessment Institute VMPR_2017 – National Food and Veterinary Risk Assessment Institute

opencc-by-4.0Mar 2020View details →

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Spain

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Spain. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005. Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – Spanish Agency for Food Safety and Nutrition; Ministry of Health VMPR_2022 – Spanish Agency for Food Safety and Nutrition VMPR_2021 – Spanish Agency for Food Safety and Nutrition VMPR_2020 – Spanish Agency for Food Safety and Nutrition VMPR_2019 – Spanish Agency for Food Safety and Nutrition VMPR_2018 – Spanish Agency for Food Safety and Nutrition VMPR_2017 – Spanish Agency for Food Safety and Nutrition; Ministry of Agriculture and Fisheries, Food and Environment

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Germany

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Germany. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005. Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – Federal Office of Consumer Protection and Food Safety VMPR_2022 – Federal Office of Consumer Protection and Food Safety VMPR_2021 – Federal Office of Consumer Protection and Food Safety VMPR_2020 – Federal Office of Consumer Protection and Food Safety VMPR_2019 – Federal Office of Consumer Protection and Food Safety VMPR_2018 – Federal Office of Consumer Protection and Food Safety VMPR_2017 – Federal Office of Consumer Protection and Food Safety

opencc-by-4.0Feb 2023View details →

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - United Kingdom in respect of Northern Ireland

This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of United Kingdom in respect of Northern Ireland. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health. For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005. Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken. Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC. The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles. Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance. Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product. Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food. Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation. Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation. Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances. For 2021 and 2022 the only United Kingdom data that were reported to EFSA were from Northern Ireland. In accordance with the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Irelandfrom the European Union and the European Atomic Energy Community, and in particular Article 5(4) of the WindsorFramework (see Joint Declaration No 1/2023 of the Union and the United Kingdom in the Joint Committee establishedby the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the EuropeanUnion and the European Atomic Energy Community of 24 March 2023, OJ L 102, 17.4.2023, p.87) in conjunction withsection 24 of Annex 2 to that Framework, for the purposes of this Regulation, references to Member States include theUnited Kingdom in respect of Northern Ireland. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: VMPR_2023 – Department of Agriculture, Environment and Rural Affairs VMPR_2022 – Department of Agriculture, Environment and Rural Affairs VMPR_2021 – Department of Agriculture, Environment and Rural Affairs

opencc-by-4.0Jan 2021View details →

Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Bosnia and Herzegovina

opencc-by-4.0Jul 2018View details →

United Kingdom results from the monitoring of pesticide residues in food

This dataset contains the analytical results of pesticide residues measured in the food products analysed by the national competent authorities. Pesticide residues resulting from the use of plant protection products on crops that are used for food or feed production may pose a risk factor for public health. For this reason, a comprehensive legislative framework has been established in the European Union (EU), which defines rules for the approval of active substances used in plant protection products, the use of plant protection products and for pesticide residues in food. In order to ensure a high level of consumer protection, legal limits, so called “maximum residue levels” or briefly “MRLs”, are established in Regulation (EC) No 396/2005. EU-harmonised MRLs are set for all pesticides covering all types of food products. A default MRL of 0.01 mg/kg is applicable for pesticides not explicitly mentioned in the MRL legislation. Regulation (EC) No 396/2005 imposes on Member States the obligation to carry out controls to ensure that food placed on the market is compliant with the legal limits. A sample is considered free of quantifiable residues if the analytes were not present in concentrations at or above the limit of quantification (LOQ). The LOQ is the smallest concentration of an analyte that can be quantified with the analytical method used to analyse the sample. It is commonly defined as the minimum concentration of the analyte in the test sample that can be determined with acceptable precision and accuracy. If a sample contains quantifiable residues but within the legally permitted limit (maximum residue level, MRL), it is described as a sample  with quantified residue levels within the legal limits (below or at the MRL) A sample is considered non-compliant with the legal limit (MRL), if the measured residue concentrations clearly exceed the legal limits, taking into account the measurement uncertainty. It is current practice that the uncertainty of the analytical measurement is taken into account before legal or administrative sanctions are imposed on food business operators for infringement of the MRL legislation.   REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: MOPER_2020 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2019 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2018 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2017 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2016 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2015 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2014 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2013 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2012 - Chemicals Regulation Directorate, Health and Safety Executive MOPER_2011 - Chemicals Regulation Directorate, Health and Safety Executive   We are seeking feedback on our open data please complete the survey at the link below: https://ec.europa.eu/eusurvey/runner/9344dfa0-f384-cb72-65f6-6c187a6d0f14

opencc-by-4.0Jan 2018View details →

Data providers package for reporting monitoring results for veterinary medicinal product residues (official data reporting phase)

This data providers package provides the data collection configuration and supporting materials for reporting veterinary medicinal product residues (VMPR) results according to Council Directive 96/23/EC of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC. These are to be used for the official data reporting phase. The package includes: Advice on the values to be reported for the mandatory fields specified for this data collection. The Standard Sample Description Version 2 XML schema definition for VMPR reporting. The STX transformation file which automatically assigns sampEventId and sampAnId when this information is not provided. The general and VMPR specific business rules applied for the automatic validation of the submitted datasets. The VMPR specific terminologies to be used for reporting analytical methods and the residues included in the scope of the analytical methods. An example of a reportable dataset following the Quick Start Reporting guide. Excel Mapping tool to convert excel files after mapping into XML document. Guidance on how to use the Excel Mapping tool. Guidance on how to run the validation report after submitting data to the DCF.

zenodo36/100

Data providers package for reporting monitoring results for veterinary medicinal product residues (2017 test phase)

This data providers package provides the data collection configuration and supporting materials for reporting veterinary medicinal product residues (VMPR) results according to Council Directive 96/23/EC of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC. These are to be used for the 2017 data reporting test phase. The package includes; Advice on the values to be reported for the mandatory fields specified for this data collection The Standard Sample Description Version 2 XML schema definition for VMPR reporting The STX transformation file which automatically assigns sampEventId and sampAnId when this information is not provided The general and VMPR specific business rules applied for the automatic validation of the submitted datasets The VMPR specific terminologies to be used for reporting analytical methods and the residues included in the scope of the analytical methods An excel tool which can support users in creating the required XML file for submission where automated data collation tools are not available and a manual for the tool

opencc-by-nd-4.0May 2017View details →

zenodo36/100

Shark-dust: Application of high-throughput DNA sequencing of processing residues for trade monitoring of threatened sharks and rays

Data repository accompanying manuscript titled of "Shark-dust: Application of high-throughput DNA sequencing of processing residues for trade monitoring of threatened sharks and rays." Prasetyo, A. P., Murray, J. M., Kurniawan, M. F. A. K., Sales, N. G., McDevitt, A. D., & Mariani, S. (2023). Shark-dust: Application of high-throughput DNA sequencing of processing residues for trade monitoring of threatened sharks and rays. Conservation Letters, 16, e12971. https://doi.org/10.1111/conl.12971

opencc-by-4.0Jul 2023View details →

ClinicalTrials.gov36/100

Improving Neuromuscular Monitoring and Reducing Residual Neuromuscular Blockade Via E-learning

ClinicalTrials.gov study NCT02925143. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →

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Italian results from the monitoring of pesticide residues in food

This dataset contains the analytical results of pesticide residues measured in the food products analysed by the national competent authorities. Pesticide residues resulting from the use of plant protection products on crops that are used for food or feed production may pose a risk factor for public health. For this reason, a comprehensive legislative framework has been established in the European Union (EU), which defines rules for the approval of active substances used in plant protection products, the use of plant protection products and for pesticide residues in food. In order to ensure a high level of consumer protection, legal limits, so called “maximum residue levels” or briefly “MRLs”, are established in Regulation (EC) No 396/2005. EU-harmonised MRLs are set for all pesticides covering all types of food products. A default MRL of 0.01 mg/kg is applicable for pesticides not explicitly mentioned in the MRL legislation. Regulation (EC) No 396/2005 imposes on Member States the obligation to carry out controls to ensure that food placed on the market is compliant with the legal limits. A sample is considered free of quantifiable residues if the analytes were not present in concentrations at or above the limit of quantification (LOQ). The LOQ is the smallest concentration of an analyte that can be quantified with the analytical method used to analyse the sample. It is commonly defined as the minimum concentration of the analyte in the test sample that can be determined with acceptable precision and accuracy. If a sample contains quantifiable residues but within the legally permitted limit (maximum residue level, MRL), it is described as a sample  with quantified residue levels within the legal limits (below or at the MRL) A sample is considered non-compliant with the legal limit (MRL), if the measured residue concentrations clearly exceed the legal limits, taking into account the measurement uncertainty. It is current practice that the uncertainty of the analytical measurement is taken into account before legal or administrative sanctions are imposed on food business operators for infringement of the MRL legislation.   REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: MOPER_2023 - Ministry of Health MOPER_2022 - Ministry of Health MOPER_2021 - Ministry of Health MOPER_2020 - Ministry of Health MOPER_2019 - Ministry of Health MOPER_2018 - Ministry of Health MOPER_2017 - Ministry of Health MOPER_2016 - Ministry of Health MOPER_2015 - Ministry of Health MOPER_2014 - Ministry of Health MOPER_2013 - Ministry of Health MOPER_2012 - Ministry of Health MOPER_2011 - Ministry of Health   We are seeking feedback on our open data please complete the survey at the link below: https://ec.europa.eu/eusurvey/runner/9344dfa0-f384-cb72-65f6-6c187a6d0f14

opencc-by-4.0Jul 2018View details →

restrictedIPD-UNDECIDEDFeb 2026View details →

Monitoring of Postoperative Residual Neuromuscular Blockade in Laparoscopic Surgery

ClinicalTrials.gov study NCT03292965. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →

Evaluation of Accelerometer-Based Neuromuscular Monitoring Reliability to Exclude Postoperative Residual Paralysis

ClinicalTrials.gov study NCT01503840. IPD Sharing: Not stated. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →

Detecting Minimal Residual Diseases (MRD) and Monitoring Clonal Evolution Using Ultrasensitive Chromosomal Aberrations Detection (UCAD) in Multiple Myeloma

ClinicalTrials.gov study NCT06302699. IPD Sharing: NO. Countries: 1. Publications: 1.