An overview of the open data available at the website of DG SANTE, European Commission: data on food safety, safety of the food chain, animal safety and health.
Annual report 2015 - European Directorate for the Quality of Medicines & Heal...Council of Europe (CoE)
This publication presents the work carried out in 2015 by the European Directorate for the Quality of Medicines & HealthCare, Council of Europe, highlighting its particular achievements.
This document summarizes the EDQM's holistic anti-counterfeiting strategy. It discusses the Medicrime Convention, an international treaty that criminalizes counterfeiting medical products. It also outlines EDQM activities like multi-sectoral training programs for health, police, and customs officials. The EDQM has trained over 300 professionals from 50 countries. Other initiatives include the Single Points of Contact network, a database of counterfeiting reports, and testing projects to identify counterfeit active pharmaceutical ingredients. The overall aim is improved information sharing and cooperation across sectors to better prevent and address counterfeiting threats.
The document summarizes the current status and future changes to novel food regulations in the EU. It discusses the four categories of novel foods, the authorization procedures, examples of novel foods that have received authorization, and how specific novel foods like algae, insects and duckweed are currently treated. It notes that the new regulations will centralize the authorization process and create a simplified procedure for traditional foods, while introducing provisions around nanomaterials and cloned animals.
Vitafoods Europe 2015: Clearer labels for consumersAxon Lawyers
The document summarizes the key aspects of the EU Food Information for Consumers Regulation, which aims to modernize and clarify food labeling requirements for consumers. It overviews the scope of the regulation, mandatory food information that must be included like ingredients and country of origin, new legibility requirements, and the upcoming mandatory nutrition declaration. It concludes that the regulation will increase administrative burden for industry but is intended to better support consumer choice and rebuilt trust following food scandals.
The document discusses the European Commission's proposals on regulating novel foods and food from cloned animals. It provides an overview of the current Novel Foods Regulation and proposes amendments, including establishing three new categories of novel foods and centralizing the authorization process. For food from cloned animals, the proposals result in a temporary ban on imports and sales due to concerns about animal welfare, low cloning efficiency, and European citizens' negative perceptions of the technique.
The long awaited new novel food regulation has finally made its very welcome arrival to update and streamline the approach to gaining approval for new food and food ingredients in the EU. It’s main benefits are to clarify the scope and definitions, to introduce a centralised procedure and to introduce a notification process for “traditional foods from third countries”. Whilst it also introduces a generic “Union List”, it also allows proprietary submissions in some cases. Although the actual legal enactment is not until January 2018, there is so much to do in the meantime. January 2016 webinar now available on demand: http://www.intertek.com/knowledge-education/new-novel-food-regulation-transition-begins/
Vitafoods marketing functional food to childrenAxon Lawyers
The document discusses marketing functional foods to children in the EU. It outlines WHO recommendations to reduce marketing of unhealthy foods to children. In the EU, health claims must meet strict criteria and not mislead consumers. National self-regulatory bodies in countries like the Netherlands set rules for food advertising to children, generally prohibiting advertising of foods high in fat, sugar, or salt for children under 12. Effectiveness of self-regulation is debated as some find additional restrictions are still needed.
Annual report 2015 - European Directorate for the Quality of Medicines & Heal...Council of Europe (CoE)
This publication presents the work carried out in 2015 by the European Directorate for the Quality of Medicines & HealthCare, Council of Europe, highlighting its particular achievements.
This document summarizes the EDQM's holistic anti-counterfeiting strategy. It discusses the Medicrime Convention, an international treaty that criminalizes counterfeiting medical products. It also outlines EDQM activities like multi-sectoral training programs for health, police, and customs officials. The EDQM has trained over 300 professionals from 50 countries. Other initiatives include the Single Points of Contact network, a database of counterfeiting reports, and testing projects to identify counterfeit active pharmaceutical ingredients. The overall aim is improved information sharing and cooperation across sectors to better prevent and address counterfeiting threats.
The document summarizes the current status and future changes to novel food regulations in the EU. It discusses the four categories of novel foods, the authorization procedures, examples of novel foods that have received authorization, and how specific novel foods like algae, insects and duckweed are currently treated. It notes that the new regulations will centralize the authorization process and create a simplified procedure for traditional foods, while introducing provisions around nanomaterials and cloned animals.
Vitafoods Europe 2015: Clearer labels for consumersAxon Lawyers
The document summarizes the key aspects of the EU Food Information for Consumers Regulation, which aims to modernize and clarify food labeling requirements for consumers. It overviews the scope of the regulation, mandatory food information that must be included like ingredients and country of origin, new legibility requirements, and the upcoming mandatory nutrition declaration. It concludes that the regulation will increase administrative burden for industry but is intended to better support consumer choice and rebuilt trust following food scandals.
The document discusses the European Commission's proposals on regulating novel foods and food from cloned animals. It provides an overview of the current Novel Foods Regulation and proposes amendments, including establishing three new categories of novel foods and centralizing the authorization process. For food from cloned animals, the proposals result in a temporary ban on imports and sales due to concerns about animal welfare, low cloning efficiency, and European citizens' negative perceptions of the technique.
The long awaited new novel food regulation has finally made its very welcome arrival to update and streamline the approach to gaining approval for new food and food ingredients in the EU. It’s main benefits are to clarify the scope and definitions, to introduce a centralised procedure and to introduce a notification process for “traditional foods from third countries”. Whilst it also introduces a generic “Union List”, it also allows proprietary submissions in some cases. Although the actual legal enactment is not until January 2018, there is so much to do in the meantime. January 2016 webinar now available on demand: http://www.intertek.com/knowledge-education/new-novel-food-regulation-transition-begins/
Vitafoods marketing functional food to childrenAxon Lawyers
The document discusses marketing functional foods to children in the EU. It outlines WHO recommendations to reduce marketing of unhealthy foods to children. In the EU, health claims must meet strict criteria and not mislead consumers. National self-regulatory bodies in countries like the Netherlands set rules for food advertising to children, generally prohibiting advertising of foods high in fat, sugar, or salt for children under 12. Effectiveness of self-regulation is debated as some find additional restrictions are still needed.
Piacenza, October 14, 2011
"Innovating Food, Innovating the Law"
Conference
ALDO PRANDINI (Università Cattolica del Sacro Cuore, Italy)
The identification of potentially emerging food safety issues: an analysis of reports published by the European Community’s Rapid Alert System for Food and Feed (RASFF)
Video: http://vimeo.com/31452234
The document discusses India's Food Safety and Standards Act of 2006. It notes that previously there were nine different laws governing the food sector administered by eight different ministries, which led to overlapping regulations. The new Act aims to consolidate food laws, establish a single regulatory body (FSSAI), and frame regulations based on science. Some key objectives of the Act include ensuring safe and wholesome food, setting science-based standards, regulating the food supply chain from manufacturing to import/export, and facilitating trade without compromising consumer safety. The Act also establishes rules for food licensing, labeling, enforcement, inspections, recalls, and penalties for non-compliance.
Vitafoods B2C communication in the funtional food Axon Lawyers
1) The document discusses the legal framework for health, nutrition, and medical claims regarding functional foods and nutraceuticals in B2C communication in the EU.
2) It outlines the differences between nutrition claims, health claims, and medical claims and the conditions for using each type of claim. Nutrition claims relate to nutrient content while health claims relate the relationship between a food and health. Medical claims are not allowed for foods.
3) The document also discusses requirements for food information to consumers regarding ingredients, legibility, and nutrition declarations according to the Food Information to Consumers Regulation.
Overview of the regulatory system for medical devices in kenyaPaulyne Wairimu
The regulatory landscape for medical devices has in recent years witnessed changes. This presentation gives an overview of the changes and the anticipated phased registration process of Medical Devices in kenya as regulatory system strengthening is developed.
Clandestines and food contamination presentation - Autumn 2015Alex Schofield
This document discusses issues related to clandestine migrants and food contamination. It provides background on relevant food safety legislation and considerations for assessing risk at borders. Key points include the public health risks of contaminated food entering the supply chain, the costly process of destroying or diverting affected goods, and challenges with intra-EU trade and international hauliers. The roles of government agencies in informing businesses of detections, prosecuting offenses, and providing coordinated advice are also covered.
The Falsified Medicines Directive - Regulation Driving DigitisationAegate
The document discusses the Falsified Medicines Directive, a new EU regulation aimed at protecting patients from counterfeit medications. It will require unique identification and authentication of prescription drug packages. This will create a digital network connecting manufacturers, distributors, pharmacies, and patients. While it imposes new costs, it also presents opportunities to improve supply chain efficiency and patient safety. Aegate advocates for national verification systems using standardized technology to ensure authentication across Europe. The regulation will transform healthcare by digitizing the pharmaceutical supply chain.
This slide deck gives background to, and an update on, the Falsified Medicines Directive and Delegated Regulation. More more information about the FMD, please visit: http://www.abpi.org.uk/our-work/falsified-medicines-directive/Pages/default.aspx
The document provides information on recent updates to the EU Falsified Medicines Directive and its requirements for safety features on medication packaging to help prevent falsified medicines. It discusses the growing problem of falsified medicines in Europe, the goals of the Falsified Medicines Directive to strengthen regulation of the pharmaceutical supply chain, and the delegated regulation outlining technical specifications for unique identifiers and anti-tampering devices that must be implemented by February 2019. It also addresses the roles and responsibilities of various stakeholders including marketing authorization holders, manufacturers, wholesalers, pharmacies and regulatory authorities in complying with the new regulations.
To a failure analysis of the pharmaceutical supply system in MoroccoIRJET Journal
This document summarizes a study on the pharmaceutical supply system in Morocco. It describes the key actors and processes in the system, including drug selection, quantification of needs, acquisition, distribution, and use. The system has faced challenges in ensuring adequate availability of drugs for patients. Issues identified include inadequate staffing leading to stockouts, poor estimates of drug needs, lack of coordination between different actors, and technical issues with inventory management and information systems. The authors analyze causes of unavailability and classify them as organizational, human, or technical to identify areas for improvement in the system's performance.
EU support to the livestock sector in EthiopiaILRI
The document summarizes EU support for Ethiopia's livestock sector over the past 10+ years, focusing on two main projects:
1. The LVC-PPD project from 2010-2015 aimed to build capacity and improve efficiency of public and private veterinary sectors through innovative approaches to animal health services.
2. The ongoing HEARD project from 2018-2022 enhances quality and quantity of integrated veterinary services at regional and local levels through training, coordination, and food safety improvements.
Both projects contribute to strengthening Ethiopia's animal health system and achieving livestock development targets in national plans. The EU support aims to improve incomes from Ethiopia's large livestock population by addressing issues like disease and lack of feed.
The development and implementation of European regulations for (fish and shel...John Bostock
Presentation given at the Symposium on seafood traceability and certification organised by Aqua-Int on behalf of the Korean Ministry of Oceans and Fisheries and Korean Fisheries Association, Busan, South Korea, 22 May 2015.
This document summarizes guidelines for registering medical devices in Kenya. It defines medical devices and in vitro diagnostic devices. It outlines the medical device lifecycle and registration requirements, including submitting documentation using the Common Submission Dossier Template format through the Pharmacy and Poisons Board's online portal. It describes risk-based classification of devices into Classes A, B, C and D and the various evaluation routes for registration based on a device's class and prior approvals in reference regulatory authorities. Exceptions for certain higher-risk devices are also noted. Contact information is provided for the Pharmacy and Poisons Board.
The document discusses proposed ways for the European Commission and other European health organizations to enhance technical collaboration on health information sharing and reduce data reporting burdens. It suggests that organizations should better coordinate their data collection efforts by aligning collections, timing, and indicators to reduce duplication; expand joint data collections in core areas and identify redundant indicators; and work to harmonize metadata, definitions, and reporting methods. The overall goals are to facilitate more automated reporting between EU and national levels, ensure stability of indicators over time, and mitigate costs of data collection.
The Falsified Medicines Directive (FMD) Rod BeardGBX Events
The document discusses the implications of the Falsified Medicines Directive (FMD) for hospital pharmacies in the UK. The FMD requires unique package numbers for all medicine packs to help identify counterfeit drugs. However, there are several operational issues with implementing this for hospital pharmacies given complexities of their supply chains. Hospitals may split drug packs, return unused stock, and source drugs through various channels. National regulations will need to address how to handle package numbers in these hospital situations to ensure successful tracking of drugs across Europe by the 2018 deadline.
In 2014, RASFF celebrated its 35th anniversary and saw improvements to its systems and procedures. There were 3,157 original notifications, of which 751 were alerts, and these resulted in 5,910 follow-ups. Notifications focused more on cases presenting significant health risks to consumers, with alert notifications increasing over 25% from 2013. RASFF also concluded initiatives like new standard operating procedures and an online notification platform, while beginning new work that will shape its future.
The document discusses standards and guidelines for tissues and cells used for human application developed by the Council of Europe. It provides an overview of the Guide to the Quality and Safety of Tissues and Cells for Human Application, which contains guidance for professionals involved in various aspects of donation, processing, storage and use of tissues and cells. The Guide aims to ensure tissues and cells used are of high quality and safety to minimize risks of disease transmission and respect ethical principles of donation.
Piacenza, October 14, 2011
"Innovating Food, Innovating the Law"
Conference
ALDO PRANDINI (Università Cattolica del Sacro Cuore, Italy)
The identification of potentially emerging food safety issues: an analysis of reports published by the European Community’s Rapid Alert System for Food and Feed (RASFF)
Video: http://vimeo.com/31452234
The document discusses India's Food Safety and Standards Act of 2006. It notes that previously there were nine different laws governing the food sector administered by eight different ministries, which led to overlapping regulations. The new Act aims to consolidate food laws, establish a single regulatory body (FSSAI), and frame regulations based on science. Some key objectives of the Act include ensuring safe and wholesome food, setting science-based standards, regulating the food supply chain from manufacturing to import/export, and facilitating trade without compromising consumer safety. The Act also establishes rules for food licensing, labeling, enforcement, inspections, recalls, and penalties for non-compliance.
Vitafoods B2C communication in the funtional food Axon Lawyers
1) The document discusses the legal framework for health, nutrition, and medical claims regarding functional foods and nutraceuticals in B2C communication in the EU.
2) It outlines the differences between nutrition claims, health claims, and medical claims and the conditions for using each type of claim. Nutrition claims relate to nutrient content while health claims relate the relationship between a food and health. Medical claims are not allowed for foods.
3) The document also discusses requirements for food information to consumers regarding ingredients, legibility, and nutrition declarations according to the Food Information to Consumers Regulation.
Overview of the regulatory system for medical devices in kenyaPaulyne Wairimu
The regulatory landscape for medical devices has in recent years witnessed changes. This presentation gives an overview of the changes and the anticipated phased registration process of Medical Devices in kenya as regulatory system strengthening is developed.
Clandestines and food contamination presentation - Autumn 2015Alex Schofield
This document discusses issues related to clandestine migrants and food contamination. It provides background on relevant food safety legislation and considerations for assessing risk at borders. Key points include the public health risks of contaminated food entering the supply chain, the costly process of destroying or diverting affected goods, and challenges with intra-EU trade and international hauliers. The roles of government agencies in informing businesses of detections, prosecuting offenses, and providing coordinated advice are also covered.
The Falsified Medicines Directive - Regulation Driving DigitisationAegate
The document discusses the Falsified Medicines Directive, a new EU regulation aimed at protecting patients from counterfeit medications. It will require unique identification and authentication of prescription drug packages. This will create a digital network connecting manufacturers, distributors, pharmacies, and patients. While it imposes new costs, it also presents opportunities to improve supply chain efficiency and patient safety. Aegate advocates for national verification systems using standardized technology to ensure authentication across Europe. The regulation will transform healthcare by digitizing the pharmaceutical supply chain.
This slide deck gives background to, and an update on, the Falsified Medicines Directive and Delegated Regulation. More more information about the FMD, please visit: http://www.abpi.org.uk/our-work/falsified-medicines-directive/Pages/default.aspx
The document provides information on recent updates to the EU Falsified Medicines Directive and its requirements for safety features on medication packaging to help prevent falsified medicines. It discusses the growing problem of falsified medicines in Europe, the goals of the Falsified Medicines Directive to strengthen regulation of the pharmaceutical supply chain, and the delegated regulation outlining technical specifications for unique identifiers and anti-tampering devices that must be implemented by February 2019. It also addresses the roles and responsibilities of various stakeholders including marketing authorization holders, manufacturers, wholesalers, pharmacies and regulatory authorities in complying with the new regulations.
To a failure analysis of the pharmaceutical supply system in MoroccoIRJET Journal
This document summarizes a study on the pharmaceutical supply system in Morocco. It describes the key actors and processes in the system, including drug selection, quantification of needs, acquisition, distribution, and use. The system has faced challenges in ensuring adequate availability of drugs for patients. Issues identified include inadequate staffing leading to stockouts, poor estimates of drug needs, lack of coordination between different actors, and technical issues with inventory management and information systems. The authors analyze causes of unavailability and classify them as organizational, human, or technical to identify areas for improvement in the system's performance.
EU support to the livestock sector in EthiopiaILRI
The document summarizes EU support for Ethiopia's livestock sector over the past 10+ years, focusing on two main projects:
1. The LVC-PPD project from 2010-2015 aimed to build capacity and improve efficiency of public and private veterinary sectors through innovative approaches to animal health services.
2. The ongoing HEARD project from 2018-2022 enhances quality and quantity of integrated veterinary services at regional and local levels through training, coordination, and food safety improvements.
Both projects contribute to strengthening Ethiopia's animal health system and achieving livestock development targets in national plans. The EU support aims to improve incomes from Ethiopia's large livestock population by addressing issues like disease and lack of feed.
The development and implementation of European regulations for (fish and shel...John Bostock
Presentation given at the Symposium on seafood traceability and certification organised by Aqua-Int on behalf of the Korean Ministry of Oceans and Fisheries and Korean Fisheries Association, Busan, South Korea, 22 May 2015.
This document summarizes guidelines for registering medical devices in Kenya. It defines medical devices and in vitro diagnostic devices. It outlines the medical device lifecycle and registration requirements, including submitting documentation using the Common Submission Dossier Template format through the Pharmacy and Poisons Board's online portal. It describes risk-based classification of devices into Classes A, B, C and D and the various evaluation routes for registration based on a device's class and prior approvals in reference regulatory authorities. Exceptions for certain higher-risk devices are also noted. Contact information is provided for the Pharmacy and Poisons Board.
The document discusses proposed ways for the European Commission and other European health organizations to enhance technical collaboration on health information sharing and reduce data reporting burdens. It suggests that organizations should better coordinate their data collection efforts by aligning collections, timing, and indicators to reduce duplication; expand joint data collections in core areas and identify redundant indicators; and work to harmonize metadata, definitions, and reporting methods. The overall goals are to facilitate more automated reporting between EU and national levels, ensure stability of indicators over time, and mitigate costs of data collection.
The Falsified Medicines Directive (FMD) Rod BeardGBX Events
The document discusses the implications of the Falsified Medicines Directive (FMD) for hospital pharmacies in the UK. The FMD requires unique package numbers for all medicine packs to help identify counterfeit drugs. However, there are several operational issues with implementing this for hospital pharmacies given complexities of their supply chains. Hospitals may split drug packs, return unused stock, and source drugs through various channels. National regulations will need to address how to handle package numbers in these hospital situations to ensure successful tracking of drugs across Europe by the 2018 deadline.
In 2014, RASFF celebrated its 35th anniversary and saw improvements to its systems and procedures. There were 3,157 original notifications, of which 751 were alerts, and these resulted in 5,910 follow-ups. Notifications focused more on cases presenting significant health risks to consumers, with alert notifications increasing over 25% from 2013. RASFF also concluded initiatives like new standard operating procedures and an online notification platform, while beginning new work that will shape its future.
The document discusses standards and guidelines for tissues and cells used for human application developed by the Council of Europe. It provides an overview of the Guide to the Quality and Safety of Tissues and Cells for Human Application, which contains guidance for professionals involved in various aspects of donation, processing, storage and use of tissues and cells. The Guide aims to ensure tissues and cells used are of high quality and safety to minimize risks of disease transmission and respect ethical principles of donation.
The document discusses efforts to harmonize regulations on botanicals between Belgium, France, and Italy. It outlines Belgium's regulatory system for botanicals and the BELFRIT project, which aims to harmonize the evaluation of botanicals in food supplements. The first phase of BELFRIT involved combining lists of authorized plants from the three countries and researching the plants' traditional uses and safety information. This resulted in a harmonized list of over 1,000 plants. Future phases will focus on further integrating the lists into national legislation and improving scientific advice exchange. The project aims to establish a coherent regulatory system across countries based on scientific evidence and traditional knowledge.
The document discusses several updates related to the REACH regulation:
- Companies can now check which substances have been registered on ECHA's website. As of today, over 2,000 of the 4,742 substances have been registered ahead of the November 2010 deadline.
- The European Environmental Bureau report found that big retailers are breaching REACH by selling products containing high levels of Substances of Very High Concern.
- The European Chemicals Agency has added the first six substances to the Authorisation list, meaning they cannot be used in the EU without specific authorisation. Sunset dates were also set for phasing out these substances.
EFRA is an EU-funded project that will develop the first analytics-enabled, green data space for AI-enabled food risk prevention. It will explore how extreme data mining, aggregation and analytics may address major scientific, economic and societal challenges associated with the safety and quality of the food that European consumers eat.
EFRA is an EU-funded project that will develop the first analytics-enabled, green data space for AI-enabled food risk prevention. It will explore how extreme data mining, aggregation and analytics may address major scientific, economic and societal challenges associated with the safety and quality of the food that European consumers eat.
The document discusses cosmetic regulation in the European Union. It provides definitions of cosmetics and outlines the regulatory process for importing cosmetics into the EU. Importers must comply with strict regulations regarding product notification, maintaining product information files, and product labeling to ensure consumer safety and quality standards are met.
This presentation provides information about the regulatory system for pharmaceutical manufacturers and GMP inspections in the European Union. It is compiled by Drug Regulations, a nonprofit organization that provides online resources for pharmaceutical professionals. The presentation explains that the EU has a harmonized system where the same rules and procedures apply in all 28 member states, which is overseen by the European Medicines Agency and national competent authorities. Manufacturers supplying products to the EU must comply with Good Manufacturing Practice standards and are subject to regular inspections.
The document provides an overview of recent developments in EU Pharmacovigilance. It discusses updates to guidelines on renewals and annual assessments. It also describes scientific advice procedures involving PRAC and updates on EU network projects like SCOPE and WEB-RADR. The document outlines progress on EudraVigilance and upcoming changes. It lists upcoming pharmacovigilance guidance documents and revisions. Major events for pharmacovigilance dialogue are also noted.
The document summarizes recent developments in EU pharmacovigilance relating to medicines for human use. It provides updates on revised guidelines for renewals and annual assessments, new scientific advice procedures involving the Pharmacovigilance Risk Assessment Committee, and two EU network projects - SCOPE and WEB-RADR - aimed at strengthening pharmacovigilance systems and utilizing social media for adverse event reporting. It also outlines achievements and upcoming activities for the EudraVigilance IT system, including a planned audit and release of new functionalities in 2017.
The document is the 2011 annual report of the Rapid Alert System for Food and Feed (RASFF). RASFF is a system managed by the European Commission that facilitates the rapid exchange of information between EU Member States about serious risks detected in food and feed. In 2011, RASFF received 9,157 notifications from inspectors reporting non-compliances with EU food and feed legislation. The report describes the RASFF system and provides an overview of the notifications handled by RASFF in 2011, including notifications related to pesticide residues.
This document provides an overview of the catering waste situation in Belgium. For category 1 catering waste from international transportation, waste is collected, sealed in containers, labeled, transported and incinerated. Collection and treatment is controlled by various authorities. For category 3 catering waste destined for composting or biogas, collection and treatment are managed regionally while the food agency controls that it is not fed to animals. Overall Belgium has implemented regulations for both categories of catering waste as outlined in the EU legislation.
1) The document discusses food safety and chain management, outlining a traditional production-oriented approach versus a consumer and market-oriented chain management approach.
2) It then summarizes EU policy on food safety, which aims to ensure stable supply of safe, quality food through harmonized standards while also supporting rural communities.
3) New developments in the Netherlands are highlighted, including reduced pesticide use through certification and training, and innovation in greenhouse technology, biological controls, and cooperative organizations.
Paul Clayton - Traceability Impacts on Future Meat Trade OpportunitiesJohn Blue
Traceability Impacts on Future Trade Opportunities - Paul Clayton, Senior Vice President of Export Services, U.S. Meat Export Federation, from the 2012 Annual Conference of the National Institute for Animal Agriculture, March 26 - 29, Denver, CO, USA.
More presentations at: http://www.trufflemedia.com/agmedia/conference/2012-decreasing-resources-increasing-regulation-advance-animal-agriculture
Safe feed and food starts with secure risk management. For this, GMP+ International offers knowledge and information through the Feed Support Products (FSP). The Feed Support Products are intended to support all (future) GMP+ certified companies when setting up their company-specific HACCP system
Prof Kristien De Paepe
Presentation at EIPG - Royal Pharmaceutical Society Scientific Symposium "Advances in Technology Impacting the Pharmaceutical Industry" at the University of Strathclyde, Glasgow 2015.
The document summarizes several projects related to developing ontologies and semantic web technologies for the agriculture domain in Hungary. It discusses 1) translating the AGROVOC thesaurus to Hungarian, 2) using AGROVOC to index documents in various projects, and 3) ongoing and planned work to develop food/farm ontologies for different applications and collaborations.
European Molecular Biology Laboratory (EMBL)- European Bioinformatics Institu...ExternalEvents
http://www.fao.org/about/meetings/wgs-on-food-safety-management/en/
Building the Database with International Isolates: European Molecular Biology Laboratory (EMBL)- European Bioinformatics Institute (EBI). Presentation from the Technical Meeting on the impact of Whole Genome Sequencing (WGS) on food safety management -23-25 May 2016, Rome, Italy.
Digital health session 4 point of care testing 7th Dec 2016David Sandbach
Thank you for sharing this information on point of care testing and digital health technologies. These innovations hold promise but also raise important questions worth discussing.
STATATHON: Unleashing the Power of Statistics in a 48-Hour Knowledge Extravag...sameer shah
"Join us for STATATHON, a dynamic 2-day event dedicated to exploring statistical knowledge and its real-world applications. From theory to practice, participants engage in intensive learning sessions, workshops, and challenges, fostering a deeper understanding of statistical methodologies and their significance in various fields."
Analysis insight about a Flyball dog competition team's performanceroli9797
Insight of my analysis about a Flyball dog competition team's last year performance. Find more: https://github.com/rolandnagy-ds/flyball_race_analysis/tree/main
Learn SQL from basic queries to Advance queriesmanishkhaire30
Dive into the world of data analysis with our comprehensive guide on mastering SQL! This presentation offers a practical approach to learning SQL, focusing on real-world applications and hands-on practice. Whether you're a beginner or looking to sharpen your skills, this guide provides the tools you need to extract, analyze, and interpret data effectively.
Key Highlights:
Foundations of SQL: Understand the basics of SQL, including data retrieval, filtering, and aggregation.
Advanced Queries: Learn to craft complex queries to uncover deep insights from your data.
Data Trends and Patterns: Discover how to identify and interpret trends and patterns in your datasets.
Practical Examples: Follow step-by-step examples to apply SQL techniques in real-world scenarios.
Actionable Insights: Gain the skills to derive actionable insights that drive informed decision-making.
Join us on this journey to enhance your data analysis capabilities and unlock the full potential of SQL. Perfect for data enthusiasts, analysts, and anyone eager to harness the power of data!
#DataAnalysis #SQL #LearningSQL #DataInsights #DataScience #Analytics
End-to-end pipeline agility - Berlin Buzzwords 2024Lars Albertsson
We describe how we achieve high change agility in data engineering by eliminating the fear of breaking downstream data pipelines through end-to-end pipeline testing, and by using schema metaprogramming to safely eliminate boilerplate involved in changes that affect whole pipelines.
A quick poll on agility in changing pipelines from end to end indicated a huge span in capabilities. For the question "How long time does it take for all downstream pipelines to be adapted to an upstream change," the median response was 6 months, but some respondents could do it in less than a day. When quantitative data engineering differences between the best and worst are measured, the span is often 100x-1000x, sometimes even more.
A long time ago, we suffered at Spotify from fear of changing pipelines due to not knowing what the impact might be downstream. We made plans for a technical solution to test pipelines end-to-end to mitigate that fear, but the effort failed for cultural reasons. We eventually solved this challenge, but in a different context. In this presentation we will describe how we test full pipelines effectively by manipulating workflow orchestration, which enables us to make changes in pipelines without fear of breaking downstream.
Making schema changes that affect many jobs also involves a lot of toil and boilerplate. Using schema-on-read mitigates some of it, but has drawbacks since it makes it more difficult to detect errors early. We will describe how we have rejected this tradeoff by applying schema metaprogramming, eliminating boilerplate but keeping the protection of static typing, thereby further improving agility to quickly modify data pipelines without fear.
ViewShift: Hassle-free Dynamic Policy Enforcement for Every Data LakeWalaa Eldin Moustafa
Dynamic policy enforcement is becoming an increasingly important topic in today’s world where data privacy and compliance is a top priority for companies, individuals, and regulators alike. In these slides, we discuss how LinkedIn implements a powerful dynamic policy enforcement engine, called ViewShift, and integrates it within its data lake. We show the query engine architecture and how catalog implementations can automatically route table resolutions to compliance-enforcing SQL views. Such views have a set of very interesting properties: (1) They are auto-generated from declarative data annotations. (2) They respect user-level consent and preferences (3) They are context-aware, encoding a different set of transformations for different use cases (4) They are portable; while the SQL logic is only implemented in one SQL dialect, it is accessible in all engines.
#SQL #Views #Privacy #Compliance #DataLake
The Ipsos - AI - Monitor 2024 Report.pdfSocial Samosa
According to Ipsos AI Monitor's 2024 report, 65% Indians said that products and services using AI have profoundly changed their daily life in the past 3-5 years.
The Building Blocks of QuestDB, a Time Series Databasejavier ramirez
Talk Delivered at Valencia Codes Meetup 2024-06.
Traditionally, databases have treated timestamps just as another data type. However, when performing real-time analytics, timestamps should be first class citizens and we need rich time semantics to get the most out of our data. We also need to deal with ever growing datasets while keeping performant, which is as fun as it sounds.
It is no wonder time-series databases are now more popular than ever before. Join me in this session to learn about the internal architecture and building blocks of QuestDB, an open source time-series database designed for speed. We will also review a history of some of the changes we have gone over the past two years to deal with late and unordered data, non-blocking writes, read-replicas, or faster batch ingestion.
4th Modern Marketing Reckoner by MMA Global India & Group M: 60+ experts on W...Social Samosa
The Modern Marketing Reckoner (MMR) is a comprehensive resource packed with POVs from 60+ industry leaders on how AI is transforming the 4 key pillars of marketing – product, place, price and promotions.
5. NFNET and Novel Food (Novel foods and
food ingredients)
The rules for authorising novel foods and food
ingredients are harmonised at European level.
Before they are placed on the market, tests
carried out by the European Food Safety
Authority...HTML XML
http://ec.europa.eu/food/safety/novel_food/catalogue
https://open-data.europa.eu/en/data/dataset/xT4Uwr
5
6. Pesticides
All foodstuffs intended for human or animal
consumption in the European Union (EU) are
subject to a maximum residue level (MRL) of
pesticides in their composition in order to
protect...HTML XML
http
://ec.europa.eu/food/plant/pesticides/eu-pesticides-d
https://open-data.europa.eu/en/data/dataset/s8QJJ4b
6
7. Agricultural and Vegetable Catalogue
The seed of varieties of agricultural and plant
species and varieties of vegetable species that
are published in the EU level common catalogue
is subject to no marketing restrictions
with...HTML XML
http://ec.europa.eu/food/plant/plant_propagation_ma
https://open-data.europa.eu/en/data/dataset/7A98oE
7
8. Food Contact Materials
Plastic materials and articles coming into contact
with foodstuffs may transfer toxic substances
which present a risk to human health. All such
substances are controlled at Community...HTML
XML
http://ec.europa.eu/food/safety/chemical_safety/food
https://open-data.europa.eu/en/data/dataset/re1HUK
8
9. European Union Register on Nutrition and
Health Claims (Health Claims)
Nutrition and health claims shall soon be
harmonised at European level in order to better
protect consumers. This Regulation establishes
the authorisation procedures required to
ensure...HTML XML
http://ec.europa.eu/food/food/labellingnutrition/claim
https://open-data.europa.eu/en/data/dataset/u3yjqnr
9
10. RASFF Window (Rapid Alert System – Food
and Feed)
European legislation ensures a consistent, high
level of food and feed safety. The European
Commission collects and publishes notifications of
any serious health risks deriving from
food...HTML XML
https://open-data.europa.eu/en/data/dataset/pghvp0
https://open-
data.europa.eu/en/data/dataset/pghvp0e6GbDsD
YrIrlESYg
10
11. Food Additives
European legislation on additives is moving
towards a single procedure for the authorisation
and evaluation of additives which takes account
of the latest evaluation measures for...HTML XML
http://ec.europa.eu/food/food/fAEF/additives/ind
ex_en.htm
https://open-
data.europa.eu/en/data/dataset/1gXgb0Yj73R4tt
DChQ5Wyg
11
12. Community List of Approved Basic Material
for Forest Reproduction Material
(Catalogue Forestry)FOREMATIS
Forestry reproductive material within the
Community may not be marketed unless it is of
one of four categories specified by legislation and
only approved basic material may be used
for...HTML XML
http://ec.europa.eu/food/plant/plant_propagation
_material/eu_marketing_requirements/forest_ma
terial_en.htm
https://open-
data.europa.eu/en/data/dataset/D8UAwJykvUjrm
nFRfyEDPw
12
13. Ontologies for datasets
The Ontology document that you can find in the
ODP explains the metadata structure of the XML
document:
13
Xls ontology
RDFs in
XML
14. 14
A URI specifying the resource the metadata is about
<rdf:Description rdf:about="http://ec.europa.eu/semantic_webgate/dataset/forestry/resource/species-16">
<forestry:abbreviation>fan</forestry:abbreviation>
<rdfs:label>Fraxinus angustifolia Vahl.</rdfs:label>
<rdf:type
rdf:resource="http://ec.europa.eu/semantic_webgate/dataset/forestry/resource/Species"/>
<forestry:id>16</forestry:id>
</rdf:Description>
Component URI
Species http://ec.europa.eu/semantic_webgate/dataset/forestry/resource/species
Semantic field Description
forestry:id key
rdfs:label The name of the species
forestry:abbreviation The abbreviation of the species