Learn how our solution offers protection against
1
Counterfeit: unauthorized product introduced into the legitimate distribution network
2
Theft: stolen from the legitimate distribution network
3
Derivations: unauthorized sale of a product based upon contractual restrictions (ex: subcontractor manufacturer)
Enterprise mobility strategy involves managing both managed and unmanaged devices and data. It focuses on 5 key areas: device/user management, app/data protection, threat protection, expense management, and enterprise/cloud integration. Symantec's solution provides comprehensive enterprise mobility management through mobile device management, mobile security, and integration with other Symantec technologies to enable secure access and protect apps and data across managed and unmanaged devices.
Solix EDMS Data Masking combined with Solix EDMS knowledgebase for the specific application, effectively scrambles, encrypts, or masks sensitive data in the test database while ensuring data format remains valid for testing purposes. The Solix pre-packages specific algorithms to handle the formats required for creating valid environment for application testing while ensuring obfuscation of personal identifiable information (PII)
Whitepaper Abstract
Any technology investment today must have an attractive ROI. This paper demonstrates the ROI associated with implementing the leading application whitelisting solution, BOUNCER by CoreTrace. Using a 500-server example, the paper outlines the various levers that generate a rapid and significant ROI. Not only does BOUNCER provide dramatically improved endpoint security, it does so at a significant savings of $938,085 over Endpoint Security 1.0 solutions — a savings of $846 per-server per-year. Moreover, the BOUNCER implementation is forecasted to pay for itself in less than 10 months.
NORONESC is an IT consultancy firm founded in 1997 located in Portugal that specializes in implementing and integrating Oracle technology solutions. It is an Oracle Certified Partner that works with clients to support their strategic decisions and implement Oracle products like E-Business Suite. NORONESC provides Oracle consulting expertise and ensures customers are successful in achieving their business goals through maximizing the return on their Oracle investments. The company focuses on delivering innovative Oracle-based solutions across various phases of projects from planning to optimization.
This document discusses the impact of serialisation and track and trace requirements on pharmaceutical packaging and supply chains. It makes three key points:
1) Serialisation legislation exists in many countries and aims to improve patient safety and reduce fraud by uniquely identifying each pharmaceutical package. This allows authentication of packages and tracking them through the supply chain.
2) Implementing full serialisation and track and trace presents major challenges for pharmaceutical supply chains. It will significantly impact companies and require changes to manufacturing, IT systems, and potentially supply chain design.
3) Pharmaceutical companies need to develop plans to manage these impacts while maintaining product supply. This includes understanding requirements, governance, capabilities, budgets, and lessons from other implementations.
The document provides information on serialization and traceability deadlines for various countries around the world. Taiwan has set a January 2018 deadline for barcode requirements on all prescription drugs. Brazil has proposed timelines of a 3 batch pilot program within 1 year, followed by 1 year of consideration and 3 years until enforcement. The EU's FMD Delegate Act goes into effect in February 2019. The United States' DSCSA requires serialization at the saleable unit and case level by manufacturers within 4 years of enactment in November 2017.
Best Practices in the Field of Serialization and Safe Supply Chain László Árvai
GS1 – and global standards • ABC – Argentina, Brasil, China and other countries – what is the world doing beyond Europe? • Serialisation – how and when? • Visibility in the supply chain – reality or myth • Patient Safety and the “Level below the Each”
Enterprise mobility strategy involves managing both managed and unmanaged devices and data. It focuses on 5 key areas: device/user management, app/data protection, threat protection, expense management, and enterprise/cloud integration. Symantec's solution provides comprehensive enterprise mobility management through mobile device management, mobile security, and integration with other Symantec technologies to enable secure access and protect apps and data across managed and unmanaged devices.
Solix EDMS Data Masking combined with Solix EDMS knowledgebase for the specific application, effectively scrambles, encrypts, or masks sensitive data in the test database while ensuring data format remains valid for testing purposes. The Solix pre-packages specific algorithms to handle the formats required for creating valid environment for application testing while ensuring obfuscation of personal identifiable information (PII)
Whitepaper Abstract
Any technology investment today must have an attractive ROI. This paper demonstrates the ROI associated with implementing the leading application whitelisting solution, BOUNCER by CoreTrace. Using a 500-server example, the paper outlines the various levers that generate a rapid and significant ROI. Not only does BOUNCER provide dramatically improved endpoint security, it does so at a significant savings of $938,085 over Endpoint Security 1.0 solutions — a savings of $846 per-server per-year. Moreover, the BOUNCER implementation is forecasted to pay for itself in less than 10 months.
NORONESC is an IT consultancy firm founded in 1997 located in Portugal that specializes in implementing and integrating Oracle technology solutions. It is an Oracle Certified Partner that works with clients to support their strategic decisions and implement Oracle products like E-Business Suite. NORONESC provides Oracle consulting expertise and ensures customers are successful in achieving their business goals through maximizing the return on their Oracle investments. The company focuses on delivering innovative Oracle-based solutions across various phases of projects from planning to optimization.
This document discusses the impact of serialisation and track and trace requirements on pharmaceutical packaging and supply chains. It makes three key points:
1) Serialisation legislation exists in many countries and aims to improve patient safety and reduce fraud by uniquely identifying each pharmaceutical package. This allows authentication of packages and tracking them through the supply chain.
2) Implementing full serialisation and track and trace presents major challenges for pharmaceutical supply chains. It will significantly impact companies and require changes to manufacturing, IT systems, and potentially supply chain design.
3) Pharmaceutical companies need to develop plans to manage these impacts while maintaining product supply. This includes understanding requirements, governance, capabilities, budgets, and lessons from other implementations.
The document provides information on serialization and traceability deadlines for various countries around the world. Taiwan has set a January 2018 deadline for barcode requirements on all prescription drugs. Brazil has proposed timelines of a 3 batch pilot program within 1 year, followed by 1 year of consideration and 3 years until enforcement. The EU's FMD Delegate Act goes into effect in February 2019. The United States' DSCSA requires serialization at the saleable unit and case level by manufacturers within 4 years of enactment in November 2017.
Best Practices in the Field of Serialization and Safe Supply Chain László Árvai
GS1 – and global standards • ABC – Argentina, Brasil, China and other countries – what is the world doing beyond Europe? • Serialisation – how and when? • Visibility in the supply chain – reality or myth • Patient Safety and the “Level below the Each”
Belgium has a large and innovative ICT sector that contributes significantly to its economy. Some key facts:
- The Belgian ICT sector is worth 20 billion euro annually and employs over 100,000 people.
- Belgium has world-class research centers like IMEC and IBBT that drive innovation in areas such as nanotechnology, e-health, and more.
- Belgium has developed expertise in 6 domains: nano-electronics, smart cards, telematics, telecom equipment, audio/video, and software.
- The government supports the ICT sector through funding for R&D projects and tax incentives.
TSP143 ECO FuturePRNT from Star MicronicsKeith Purvey
This document introduces the TSP100 ECO point-of-sale printer. It is designed and marketed as an eco-friendly printer solution. Key features include major power savings of up to 40% compared to competitors, integrated carbon offsetting for 5 years of use, and several paper saving tools. These allow for reduced paper consumption of up to 70%. The TSP100 ECO also uses recyclable packaging and materials. It is priced competitively to standard non-eco printers and includes a 4-year warranty. The printer is positioned as providing eco-friendly benefits without increased costs for retailers.
APICS Country Supply Chain Award - 19/02 - Milan - Presentation of Alberto Della Chiesa, CPIM, STMicroelectronics, Group Vice President, Company Supply Chain Management
Counterfeit Products are epidemic in all product categories, but - unlike luxury goods – fakes and counterfeit pharmaceutical products endanger lives, either through their lack of active ingredients or the inclusion of harmful substances.
(The WHO estimates that over 30% of pharmaceuticals in developing countries are fake).
In this document, we would like to request your support for a field study of our latest mobile visual forensics application that is intended to provide quick, reliable and cost effective identification of counterfeit pharmaceutical goods.
http://www.e-mundo.de
Counterfeit Herbal Medicine adulterated with chemical drugs in Indonesia: NAD...Premier Publishers
Herbal medicine is widely used in Indonesia. Thus, counterfeit herbal medicines are a great concern given the negative impact to individual and population health. This paper used data drawn from the National Agency of Drug and Food Control (NADFC/BPOM)of Indonesia to describe the counterfeit trend against registered herbal drugs from 2011 to 2014, and further analyses were performed to discover the types of the fraud, the impact to the health and conventional drugs that could be used as substitutes for herbal drugs. The research found that the amount of falsified medicines is increasing along with the increasing number of registered herbal drugs. From the data obtained, similar falsified herbal drugs were identified for both life style drugs (51%) and health-related condition drugs (49%). In addition, almost all falsified herbal drugs are adulterations plus tampering (81%). The most significant substitute chemical drug is paracetamol.
GS1 UK Healthcare Conference - Masterclass Presentation - Bhulesh VadherGS1 UK
This document discusses the Falsified Medicines Directive (FMD) and its implications for hospital pharmacy from a UK perspective. It notes that an estimated 1-10% of medicines globally are counterfeit and the FMD aims to solve this problem through serialization and authentication of medicine packages. A hospital pharmacy pilot found that authentication was possible at various stages with a detection rate of 100% and authentication rates of 60-70%. Staff adapted well to the new system. The FMD will require enormous changes to hospital pharmacy practice but also presents opportunities to improve safety and efficiency.
From documents to datasets and back: challenges and solutions Jan Voskuil
The upcoming effectuation of the IDMP directive (EU) forces pharma companies to submit datasets instead of documents. Based on state of the art entity extraction software, a solution is developed that generates those parts of the dataset that can be obtained from the text. The presentation describes some of the major challenges that had to be overcome and details the solutions that were found. It presents some results and describes the major business requirements that need to be met. Recognizing named entities, such as headache and nausea, in the text is not enough. The extraction software needs to be embedded in a layer of software that analyses the text and recognizes which entities are the value of which properties.
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.
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.
One of the results of the recently approved EU Falsified Medicines Directive imposes the application of a Unique Product Identifier and a Tamper Evidence Feature. This is only the top of the iceberg. It is not just printing a code and adding a label on a box, it means Authentication Data Flow, design the proper IT architecture, learn a new way of handling the products with a precise deadline: February 2019.
From this date all prescription products (with some exceptions)
must be serialized and data must be loaded into the EU hub.
Sharp can support you, thanks to 8 years of experience, 2 billions of sales units serialized to date, 4 plants already serializing for USA (US Drug Quality Security Act enforced from 27th November 2017), China, Brazil, South Corea.
Background to the Falsified Medicines Directive and the Delegated RegulationGS1 UK
The document discusses the Falsified Medicines Directive and Delegated Regulation, which aim to secure the pharmaceutical supply chain and reduce counterfeit medicines. It outlines key aspects of the new regulations, including unique identifiers and tamper-evident packaging for prescription medicines. Verification of authenticity will occur at wholesale distributors and dispensing points. National repositories will store product information to enable verification. Implementation poses scale and connectivity challenges across the complex supply chain. Wider benefits may include improved patient safety, monitoring, and reducing fraud. Flexibilities allow country-specific requirements and earlier verification in some settings like hospitals.
SMi Group announces the return of its 11th annual Pharmaceutical Logistics conference to London on the 18th- 19th May 2017. Outsourcing logistics tasks to third parties has been observed as an emerging trend in the global market and it is only expected to gain momentum in the coming years
The document summarizes the minutes from a CPS Council meeting held in November 2016. Key discussions included:
- Negotiations on the financial package for 2017/18 which may be difficult due to Brexit and other budget pressures.
- Updates on the transfer of certain pharmaceutical care and administration medicines from secondary to primary care.
- A presentation on the Falsified Medicines Directive which aims to secure the pharmaceutical supply chain through unique identifiers and anti-tampering devices on drug packaging.
- Various other agenda items like the Inverclyde MAS pilot, continuous improvement efforts, and the upcoming AGM. The document provides an overview of the discussions without going into detail on the outcomes or decisions
IFPMA-TFDA Workshop on Couterfeit Medicines
‘Integrated Approach Against Fake Medicines’
Session 2: Supply Chain Integrity
On 6th February 2015
At Taipei International Convention Center
Taipei, Taiwan
RyMat Inc.: A Look At Generic vs. Brand PharmaceuticalsStuart Silverman
The document discusses generics vs brand name drugs and risks associated with generics. It notes that generics must have the same active ingredients and be within 10-25% of brand name drug concentrations to be approved. However, generics may have different inactive ingredients and manufacturing processes can vary, resulting in differences between generics. The document outlines issues found at some generic drug manufacturing plants in India and China, including falsifying data, poor quality control, and hiding failed test results. It warns that not all generics are equal and some imported from these countries may pose risks.
Hans van Bruggen | Semantic interoperability to manage medicinal data and exc...semanticsconference
This document discusses the importance of managing medicinal data within and between the pharmaceutical industry and regulatory agencies. It outlines challenges such as ensuring consistent high-quality drug production, evaluating drug safety and efficacy, and exchanging information accurately. Examples are given where failures in data management led to health issues or drug shortages. The document argues that integrating systems using technical and semantic interoperability standards, and defining a single source of truth for medicinal product data, can help address these challenges by improving information sharing, signal detection, and corrective actions.
The pharmaceutical supply chain is complex and highly regulated. It involves multiple players from drug discovery and development to manufacturing and distribution. Ensuring patient safety is the top priority and challenge, as the supply chain is vulnerable to counterfeiting and issues regarding product quality. Emerging technologies around tracking and authentication aim to address these problems. Regulation and compliance add further complexity, as the industry works to balance costs and efficiencies with ethical and safety requirements.
Drug discovery process style 5 powerpoint presentation templatesSlideTeam.net
The document describes the key stages in the drug discovery process, including cellular and genetic target identification, compound synthesis and isolation, high-throughput screening, lead optimization, preclinical testing in animal models and in vitro/in vivo studies, and clinical trials in humans. The flow diagram shows the iterative process moving from early research to identify biological targets through compound development and testing, culminating in clinical evaluation and potential approval of new therapeutics.
Complexity and Risk: Effective Business Community Management through Integrationjgatrell
Increased economic pressures and continuous changes in market dynamics businesses need to make decisions in real-time based on information from their suppliers and business partners. Global business communities are often at risk without visibility into key indicators which can impact their bottom line due to integration challenges within their back office and throughout the community.
This session will outline emerging trends and investments in managing business communities and illustrate how visibility integration and automation improved businesses execution. Real-time visibility will reduce the business impact from such events as compliance, charge backs, fulfillment or supplier rating issues caused by data quality issues and limited visibility due to integration gaps. These events can drastically stall the order-to-cash lifecycle and impact customer relationships.
ConnectM is a leading global M2M technology solutions and services company with over 80 man-years of M2M expertise. It has managed over 60,000 assets through its M2M platform, including 30,000 telecom towers and 25,000 buildings. ConnectM has 30+ customers that are mostly large multinational corporations. It has won several awards and has a patent-pending technology with ready-to-use M2M frameworks and components.
This document discusses how data-centric systems are increasingly needed to manage growing data volumes and velocities. It presents the Data Distribution Service (DDS) as a solution, which defines a common data model and quality of service contracts. DDS provides a standardized publish-subscribe architecture around the shared data model for improved integration and interoperability compared to traditional message-based approaches. It has been adopted for several major systems due to reducing programming effort, costs, and risks.
Belgium has a large and innovative ICT sector that contributes significantly to its economy. Some key facts:
- The Belgian ICT sector is worth 20 billion euro annually and employs over 100,000 people.
- Belgium has world-class research centers like IMEC and IBBT that drive innovation in areas such as nanotechnology, e-health, and more.
- Belgium has developed expertise in 6 domains: nano-electronics, smart cards, telematics, telecom equipment, audio/video, and software.
- The government supports the ICT sector through funding for R&D projects and tax incentives.
TSP143 ECO FuturePRNT from Star MicronicsKeith Purvey
This document introduces the TSP100 ECO point-of-sale printer. It is designed and marketed as an eco-friendly printer solution. Key features include major power savings of up to 40% compared to competitors, integrated carbon offsetting for 5 years of use, and several paper saving tools. These allow for reduced paper consumption of up to 70%. The TSP100 ECO also uses recyclable packaging and materials. It is priced competitively to standard non-eco printers and includes a 4-year warranty. The printer is positioned as providing eco-friendly benefits without increased costs for retailers.
APICS Country Supply Chain Award - 19/02 - Milan - Presentation of Alberto Della Chiesa, CPIM, STMicroelectronics, Group Vice President, Company Supply Chain Management
Counterfeit Products are epidemic in all product categories, but - unlike luxury goods – fakes and counterfeit pharmaceutical products endanger lives, either through their lack of active ingredients or the inclusion of harmful substances.
(The WHO estimates that over 30% of pharmaceuticals in developing countries are fake).
In this document, we would like to request your support for a field study of our latest mobile visual forensics application that is intended to provide quick, reliable and cost effective identification of counterfeit pharmaceutical goods.
http://www.e-mundo.de
Counterfeit Herbal Medicine adulterated with chemical drugs in Indonesia: NAD...Premier Publishers
Herbal medicine is widely used in Indonesia. Thus, counterfeit herbal medicines are a great concern given the negative impact to individual and population health. This paper used data drawn from the National Agency of Drug and Food Control (NADFC/BPOM)of Indonesia to describe the counterfeit trend against registered herbal drugs from 2011 to 2014, and further analyses were performed to discover the types of the fraud, the impact to the health and conventional drugs that could be used as substitutes for herbal drugs. The research found that the amount of falsified medicines is increasing along with the increasing number of registered herbal drugs. From the data obtained, similar falsified herbal drugs were identified for both life style drugs (51%) and health-related condition drugs (49%). In addition, almost all falsified herbal drugs are adulterations plus tampering (81%). The most significant substitute chemical drug is paracetamol.
GS1 UK Healthcare Conference - Masterclass Presentation - Bhulesh VadherGS1 UK
This document discusses the Falsified Medicines Directive (FMD) and its implications for hospital pharmacy from a UK perspective. It notes that an estimated 1-10% of medicines globally are counterfeit and the FMD aims to solve this problem through serialization and authentication of medicine packages. A hospital pharmacy pilot found that authentication was possible at various stages with a detection rate of 100% and authentication rates of 60-70%. Staff adapted well to the new system. The FMD will require enormous changes to hospital pharmacy practice but also presents opportunities to improve safety and efficiency.
From documents to datasets and back: challenges and solutions Jan Voskuil
The upcoming effectuation of the IDMP directive (EU) forces pharma companies to submit datasets instead of documents. Based on state of the art entity extraction software, a solution is developed that generates those parts of the dataset that can be obtained from the text. The presentation describes some of the major challenges that had to be overcome and details the solutions that were found. It presents some results and describes the major business requirements that need to be met. Recognizing named entities, such as headache and nausea, in the text is not enough. The extraction software needs to be embedded in a layer of software that analyses the text and recognizes which entities are the value of which properties.
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.
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.
One of the results of the recently approved EU Falsified Medicines Directive imposes the application of a Unique Product Identifier and a Tamper Evidence Feature. This is only the top of the iceberg. It is not just printing a code and adding a label on a box, it means Authentication Data Flow, design the proper IT architecture, learn a new way of handling the products with a precise deadline: February 2019.
From this date all prescription products (with some exceptions)
must be serialized and data must be loaded into the EU hub.
Sharp can support you, thanks to 8 years of experience, 2 billions of sales units serialized to date, 4 plants already serializing for USA (US Drug Quality Security Act enforced from 27th November 2017), China, Brazil, South Corea.
Background to the Falsified Medicines Directive and the Delegated RegulationGS1 UK
The document discusses the Falsified Medicines Directive and Delegated Regulation, which aim to secure the pharmaceutical supply chain and reduce counterfeit medicines. It outlines key aspects of the new regulations, including unique identifiers and tamper-evident packaging for prescription medicines. Verification of authenticity will occur at wholesale distributors and dispensing points. National repositories will store product information to enable verification. Implementation poses scale and connectivity challenges across the complex supply chain. Wider benefits may include improved patient safety, monitoring, and reducing fraud. Flexibilities allow country-specific requirements and earlier verification in some settings like hospitals.
SMi Group announces the return of its 11th annual Pharmaceutical Logistics conference to London on the 18th- 19th May 2017. Outsourcing logistics tasks to third parties has been observed as an emerging trend in the global market and it is only expected to gain momentum in the coming years
The document summarizes the minutes from a CPS Council meeting held in November 2016. Key discussions included:
- Negotiations on the financial package for 2017/18 which may be difficult due to Brexit and other budget pressures.
- Updates on the transfer of certain pharmaceutical care and administration medicines from secondary to primary care.
- A presentation on the Falsified Medicines Directive which aims to secure the pharmaceutical supply chain through unique identifiers and anti-tampering devices on drug packaging.
- Various other agenda items like the Inverclyde MAS pilot, continuous improvement efforts, and the upcoming AGM. The document provides an overview of the discussions without going into detail on the outcomes or decisions
IFPMA-TFDA Workshop on Couterfeit Medicines
‘Integrated Approach Against Fake Medicines’
Session 2: Supply Chain Integrity
On 6th February 2015
At Taipei International Convention Center
Taipei, Taiwan
RyMat Inc.: A Look At Generic vs. Brand PharmaceuticalsStuart Silverman
The document discusses generics vs brand name drugs and risks associated with generics. It notes that generics must have the same active ingredients and be within 10-25% of brand name drug concentrations to be approved. However, generics may have different inactive ingredients and manufacturing processes can vary, resulting in differences between generics. The document outlines issues found at some generic drug manufacturing plants in India and China, including falsifying data, poor quality control, and hiding failed test results. It warns that not all generics are equal and some imported from these countries may pose risks.
Hans van Bruggen | Semantic interoperability to manage medicinal data and exc...semanticsconference
This document discusses the importance of managing medicinal data within and between the pharmaceutical industry and regulatory agencies. It outlines challenges such as ensuring consistent high-quality drug production, evaluating drug safety and efficacy, and exchanging information accurately. Examples are given where failures in data management led to health issues or drug shortages. The document argues that integrating systems using technical and semantic interoperability standards, and defining a single source of truth for medicinal product data, can help address these challenges by improving information sharing, signal detection, and corrective actions.
The pharmaceutical supply chain is complex and highly regulated. It involves multiple players from drug discovery and development to manufacturing and distribution. Ensuring patient safety is the top priority and challenge, as the supply chain is vulnerable to counterfeiting and issues regarding product quality. Emerging technologies around tracking and authentication aim to address these problems. Regulation and compliance add further complexity, as the industry works to balance costs and efficiencies with ethical and safety requirements.
Drug discovery process style 5 powerpoint presentation templatesSlideTeam.net
The document describes the key stages in the drug discovery process, including cellular and genetic target identification, compound synthesis and isolation, high-throughput screening, lead optimization, preclinical testing in animal models and in vitro/in vivo studies, and clinical trials in humans. The flow diagram shows the iterative process moving from early research to identify biological targets through compound development and testing, culminating in clinical evaluation and potential approval of new therapeutics.
Complexity and Risk: Effective Business Community Management through Integrationjgatrell
Increased economic pressures and continuous changes in market dynamics businesses need to make decisions in real-time based on information from their suppliers and business partners. Global business communities are often at risk without visibility into key indicators which can impact their bottom line due to integration challenges within their back office and throughout the community.
This session will outline emerging trends and investments in managing business communities and illustrate how visibility integration and automation improved businesses execution. Real-time visibility will reduce the business impact from such events as compliance, charge backs, fulfillment or supplier rating issues caused by data quality issues and limited visibility due to integration gaps. These events can drastically stall the order-to-cash lifecycle and impact customer relationships.
ConnectM is a leading global M2M technology solutions and services company with over 80 man-years of M2M expertise. It has managed over 60,000 assets through its M2M platform, including 30,000 telecom towers and 25,000 buildings. ConnectM has 30+ customers that are mostly large multinational corporations. It has won several awards and has a patent-pending technology with ready-to-use M2M frameworks and components.
This document discusses how data-centric systems are increasingly needed to manage growing data volumes and velocities. It presents the Data Distribution Service (DDS) as a solution, which defines a common data model and quality of service contracts. DDS provides a standardized publish-subscribe architecture around the shared data model for improved integration and interoperability compared to traditional message-based approaches. It has been adopted for several major systems due to reducing programming effort, costs, and risks.
Hadoop World 2011: Security Considerations for Hadoop Deployments - Jeremy Gl...Cloudera, Inc.
Security in a distributed environment is a growing concern for most industries. Few face security challenges like the Defense Community, who must balance complex security constraints with timeliness and accuracy. We propose to briefly discuss the security paradigms defined in DCID 6/3 by NSA for secure storage and access of data (the “Protection Level” system). In addition, we will describe the implications of each level on the Hadoop architecture and various patterns organizations can implement to meet these requirements within the Hadoop ecosystem. We conclude with our “wish list” of features essential to meet the federal security requirements.
What are the technology challenges? What are the new possibilities, applications, services or features that will empower mobile workers even more?
Experts on these subjects will cover several interesting topics: Mobile data, Device Management, Mobile Security and Mobile Enterprise Apps.
Belgacom MAC by Jan Paesen - Director Mobility at Belgacom
The document discusses M2M (machine-to-machine) communication and the Eclipse M2M Industry Workgroup's efforts to standardize and promote open interoperability in the field. It outlines key trends driving growth in the M2M market, challenges facing development, and the Workgroup's goals of providing open communication protocols, application frameworks, tools, and a developer portal to support an ecosystem of integrated M2M solutions. Use cases illustrate potential applications in vertical markets like logistics, medical services, and more.
ITExpo West Conference Highlights from Alan Quayle 2012Alan Quayle
This document summarizes highlights from the IPExpo West 2012 conference on machine-to-machine (M2M) technologies. Digi was recognized as the overall winner in the M2M platform battle for its device cloud platform. Eurotech and FedEx SenseAware were joint winners for best enterprise deployment. Kore won for best service provider platform. The document discusses various company solutions and products showcased at the event, including Digi's device cloud platform, FedEx SenseAware temperature monitoring solution, and AT&T's efforts to simplify M2M.
Symantec Enterprise Mobility - Mobile World Congress February 2012Symantec
At Mobile World Congress 2012, Symantec announced significant advances in core areas of its enterprise mobility strategy across Android, iOS and Windows Phone 7 platforms. These advances help customers secure mobile data and enable business productivity across both corporate managed and personally owned unmanaged devices by providing cross-platform, multi-application protection.
The document discusses Midokura's cloud networking solution for industrial enterprises. It allows companies to connect, secure and gain insights from IoT devices and industrial systems. Key benefits include faster innovation, improved efficiency, stronger security, and freeing up IT/OT teams to focus on strategic work. Midokura provides the network infrastructure and tools to manage thousands of connected devices across factories, warehouses and enterprise networks.
SmartConnect Technologies is an enterprise communications and solutions company founded in 2010 with offices in India, Dubai, and South Africa. It focuses on unified interaction management across channels and industries. The company offers mobile solutions through its SmartMobi platform, which provides mobile device management, application development, and integration with enterprise systems. SmartConnect has over 30 employees including an experienced management team with over 100 years of collective experience in unified interaction management.
The Changes In Service Delivery With Cloud ComputingMartin Hingley
The document discusses the growth of cloud computing and its impact on IT service delivery. It provides revenue projections for different cloud service models like SaaS, IaaS, and PaaS. Examples of cloud reference architectures from IBM, HP, Fujitsu, and Dell are presented. The role of internal IT is changing with more focus on compliance, security and data protection with the adoption of public and hybrid cloud services. Case studies of enterprises adopting cloud and forecasts for different cloud service markets are also summarized.
The document discusses Wind River's medical device solutions including their VxWorks, Linux, and Android operating systems. It highlights key medical market trends around cost pressures, safety, security, and interconnectivity. Wind River provides services across the medical value chain from silicon to hospitals. Their professional services help address technology and process needs through consulting, turnkey design, and certification services.
M2M Presentation at Telecom Council of Silicon ValleyDaniel Kellmereit
The document discusses the promise and challenges of M2M technology and its application across various industries. It notes that while M2M leads to improvements in productivity, efficiency and transparency, its adoption has been slowed by challenges like regulation, cost, technology maturity and fragmented solutions. However, drivers like falling hardware costs, ubiquitous network access and the rise of cloud computing are fueling more widespread adoption. Key growth areas are expected to be intelligent buildings, telematics and healthcare. The document advocates for standardization while also noting carriers should actively partner to develop platforms and solutions.
International approaches to critical information infrastructure protection ...owaspindia
This document discusses international cooperation on critical infrastructure protection (CIP) and trustworthy information and communications technology (ICT). It describes the BIC project, which aims to identify challenges to EU and global trust and security, and facilitate collaboration between organizations. Key issues discussed include monitoring critical infrastructure ecosystems, detection of anomalies, secure notification systems, metrics for quantifying protection, and response strategies. International cooperation is needed for technologies, threat information sharing, and data management standards regarding acquisition, dissemination, storage, and access.
This document summarizes a presentation on master data management (MDM) and its role in establishing a strong service-oriented architecture (SOA) foundation. MDM addresses issues like inconsistent, low quality distributed data by aggregating, mapping, normalizing and standardizing data. Implementation options include centralized or distributed topologies and different data merge models. MDM provides benefits like improved data quality and trust but requires investments to identify systems of record and move to single updates where possible.
Security Patterns How To Make Security Arch Easy To ConsumeJeff Johnson
A challenge security professionals often face is ensuring security is aligned with the business strategy. Enterprise Security Architecture can solve that problem, but to do so you need a way to make it easy for the rest of IT to follow the security architecture. Security Patterns is one solution to that problem.
Inter op nyc_mahbubul alam_october 2012Mahbubul Alam
This document discusses the growing field of machine-to-machine (M2M) communications and the Internet of Things (IoT). It notes that by 2020 there will be almost half a billion connected devices in the security sector alone. Cisco's M2M and IoT solutions help enable new business models by providing remote monitoring of devices and assets using existing management networks. The document highlights Cisco's ruggedized M2M gateway and wireless products that securely connect devices in industries like oil and gas, transportation, manufacturing and mining.
Cyber security in real-time systems is an evolving area with several obstacles and open issues still remaining. [1] Adoption of cloud computing lessons is limited and implementation experiences are narrow, while security and risk management methods are still immature. [2] Best practices are emerging but gaps exist, and the views of regulators and auditors on legal and regulatory issues are still unclear. [3] Overcoming these challenges will require further work to develop robust and accepted security policies, access control, encryption, and flexibility in contractual agreements.
1) Deutsche Telekom is launching a BusinessMarketplace platform to provide SMB customers easy access to cloud applications. The platform will use OpenStack as the underlying infrastructure layer.
2) The BusinessMarketplace will offer a curated selection of third-party applications that are secured, integrated and managed by Deutsche Telekom on behalf of customers. This provides customers compliance with German regulations.
3) For partners, the BusinessMarketplace provides a new sales channel to reach Deutsche Telekom's over 3 million SMB customers. The OpenStack infrastructure also allows partners to more easily integrate their applications and have them hosted on a stable, scalable platform.
Similar to Pharma datamatrix identification and serialisation (20)
L'avvento della supply chain collaborativa.
Un portafoglio di soluzioni.
Zetes mira a rendere possibile la supply chain collaborativa. A partire dallo stabilimento di produzione per arrivare al punto vendita, le sue soluzioni sono state sviluppate per risolvere le difficoltà di ogni specifico mercato:
ZetesAtlas, per le operazioni sulla linea di packaging
ZetesMedea, per l’efficienza logistica di magazzino
ZetesChronos per la puntualità delle consegne
ZetesAtlas per la gestione in-store
ZetesOlympus repository di tracciamento.
Supply chain efficiency and traceability Zetes srl
Managing the supply chain from the packing line to the store is what we do and this leaflet explains how in just 1 page.
Over 30 years of experience at your disposal.
Gestire la supply chain dalla linea di impacchettamento in produzione fino all'inventario in negozio.
30 anni di esperienza a vostra disposizione.
Newsletter Zetes con sviluppi della tecnologia vocale, serializzazione e tracciabilità nel settore farmaceutico, tempi di verifica spedizioni ridotti del 30%
Tracciabilità e Identificazione AutomaticaZetes srl
Newsletter aziendale propone una selezione di articoli, novità sui prodotti e case studies.
Maggio 2012
Identificazione vocale e con immagini
Tracciabilità e Visibilità per Retailers
Prova di avvenuta consegna
RFID is often most efficiently used when combined with other technologies. In this way, it can then become a route to completing and enhancing an existing solution.
Contrary to what one might think, the implementation of RFID does not trigger a
revolution of all operational processes - it can be integrated very smoothly into existing
ones and work in parallel with other solutions.
The document discusses asset management and tracking across various industries. It begins by explaining how asset tracking can lower costs by ensuring assets are in the right place at the right time. It then provides examples of how asset tracking solutions have been implemented in healthcare, food and beverage production, retail, and logistics to improve efficiency, accountability and reduce losses. The document concludes by stating that asset utilization tracking will become more common as technology costs decrease and real-time information improves decision making.
The document provides an overview of Zetes, a company that offers identification and supply chain solutions. Zetes has over 25 years of experience, a presence in 15 European countries, and over 1000 employees. It offers goods and people identification solutions to help customers with traceability, efficiency, quality and visibility across various industries and parts of the supply chain, including manufacturing, distribution, transport, and retail. Zetes also has a proven track record in secure identity documents and travel documents for governments and private organizations.
The Most Inspiring Entrepreneurs to Follow in 2024.pdfthesiliconleaders
In a world where the potential of youth innovation remains vastly untouched, there emerges a guiding light in the form of Norm Goldstein, the Founder and CEO of EduNetwork Partners. His dedication to this cause has earned him recognition as a Congressional Leadership Award recipient.
NIMA2024 | De toegevoegde waarde van DEI en ESG in campagnes | Nathalie Lam |...BBPMedia1
Nathalie zal delen hoe DEI en ESG een fundamentele rol kunnen spelen in je merkstrategie en je de juiste aansluiting kan creëren met je doelgroep. Door middel van voorbeelden en simpele handvatten toont ze hoe dit in jouw organisatie toegepast kan worden.
Industrial Tech SW: Category Renewal and CreationChristian Dahlen
Every industrial revolution has created a new set of categories and a new set of players.
Multiple new technologies have emerged, but Samsara and C3.ai are only two companies which have gone public so far.
Manufacturing startups constitute the largest pipeline share of unicorns and IPO candidates in the SF Bay Area, and software startups dominate in Germany.
Storytelling is an incredibly valuable tool to share data and information. To get the most impact from stories there are a number of key ingredients. These are based on science and human nature. Using these elements in a story you can deliver information impactfully, ensure action and drive change.
[To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
This PowerPoint compilation offers a comprehensive overview of 20 leading innovation management frameworks and methodologies, selected for their broad applicability across various industries and organizational contexts. These frameworks are valuable resources for a wide range of users, including business professionals, educators, and consultants.
Each framework is presented with visually engaging diagrams and templates, ensuring the content is both informative and appealing. While this compilation is thorough, please note that the slides are intended as supplementary resources and may not be sufficient for standalone instructional purposes.
This compilation is ideal for anyone looking to enhance their understanding of innovation management and drive meaningful change within their organization. Whether you aim to improve product development processes, enhance customer experiences, or drive digital transformation, these frameworks offer valuable insights and tools to help you achieve your goals.
INCLUDED FRAMEWORKS/MODELS:
1. Stanford’s Design Thinking
2. IDEO’s Human-Centered Design
3. Strategyzer’s Business Model Innovation
4. Lean Startup Methodology
5. Agile Innovation Framework
6. Doblin’s Ten Types of Innovation
7. McKinsey’s Three Horizons of Growth
8. Customer Journey Map
9. Christensen’s Disruptive Innovation Theory
10. Blue Ocean Strategy
11. Strategyn’s Jobs-To-Be-Done (JTBD) Framework with Job Map
12. Design Sprint Framework
13. The Double Diamond
14. Lean Six Sigma DMAIC
15. TRIZ Problem-Solving Framework
16. Edward de Bono’s Six Thinking Hats
17. Stage-Gate Model
18. Toyota’s Six Steps of Kaizen
19. Microsoft’s Digital Transformation Framework
20. Design for Six Sigma (DFSS)
To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations
HR search is critical to a company's success because it ensures the correct people are in place. HR search integrates workforce capabilities with company goals by painstakingly identifying, screening, and employing qualified candidates, supporting innovation, productivity, and growth. Efficient talent acquisition improves teamwork while encouraging collaboration. Also, it reduces turnover, saves money, and ensures consistency. Furthermore, HR search discovers and develops leadership potential, resulting in a strong pipeline of future leaders. Finally, this strategic approach to recruitment enables businesses to respond to market changes, beat competitors, and achieve long-term success.
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Anny Serafina Love - Letter of Recommendation by Kellen Harkins, MS.AnnySerafinaLove
This letter, written by Kellen Harkins, Course Director at Full Sail University, commends Anny Love's exemplary performance in the Video Sharing Platforms class. It highlights her dedication, willingness to challenge herself, and exceptional skills in production, editing, and marketing across various video platforms like YouTube, TikTok, and Instagram.
Navigating the world of forex trading can be challenging, especially for beginners. To help you make an informed decision, we have comprehensively compared the best forex brokers in India for 2024. This article, reviewed by Top Forex Brokers Review, will cover featured award winners, the best forex brokers, featured offers, the best copy trading platforms, the best forex brokers for beginners, the best MetaTrader brokers, and recently updated reviews. We will focus on FP Markets, Black Bull, EightCap, IC Markets, and Octa.
Brian Fitzsimmons on the Business Strategy and Content Flywheel of Barstool S...Neil Horowitz
On episode 272 of the Digital and Social Media Sports Podcast, Neil chatted with Brian Fitzsimmons, Director of Licensing and Business Development for Barstool Sports.
What follows is a collection of snippets from the podcast. To hear the full interview and more, check out the podcast on all podcast platforms and at www.dsmsports.net
Discover timeless style with the 2022 Vintage Roman Numerals Men's Ring. Crafted from premium stainless steel, this 6mm wide ring embodies elegance and durability. Perfect as a gift, it seamlessly blends classic Roman numeral detailing with modern sophistication, making it an ideal accessory for any occasion.
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Part 2 Deep Dive: Navigating the 2024 Slowdownjeffkluth1
Introduction
The global retail industry has weathered numerous storms, with the financial crisis of 2008 serving as a poignant reminder of the sector's resilience and adaptability. However, as we navigate the complex landscape of 2024, retailers face a unique set of challenges that demand innovative strategies and a fundamental shift in mindset. This white paper contrasts the impact of the 2008 recession on the retail sector with the current headwinds retailers are grappling with, while offering a comprehensive roadmap for success in this new paradigm.
Profiles of Iconic Fashion Personalities.pdfTTop Threads
The fashion industry is dynamic and ever-changing, continuously sculpted by trailblazing visionaries who challenge norms and redefine beauty. This document delves into the profiles of some of the most iconic fashion personalities whose impact has left a lasting impression on the industry. From timeless designers to modern-day influencers, each individual has uniquely woven their thread into the rich fabric of fashion history, contributing to its ongoing evolution.
Discover innovative uses of Revit in urban planning and design, enhancing city landscapes with advanced architectural solutions. Understand how architectural firms are using Revit to transform how processes and outcomes within urban planning and design fields look. They are supplementing work and putting in value through speed and imagination that the architects and planners are placing into composing progressive urban areas that are not only colorful but also pragmatic.
Presentation by Herman Kienhuis (Curiosity VC) on Investing in AI for ABS Alu...Herman Kienhuis
Presentation by Herman Kienhuis (Curiosity VC) on developments in AI, the venture capital investment landscape and Curiosity VC's approach to investing, at the alumni event of Amsterdam Business School (University of Amsterdam) on June 13, 2024 in Amsterdam.
4. • Goods ID (65%) & People ID (35%) specialists
Zetes – Fact Sheet
• Public since Nov. 2005 (Euronext: ZTS)
• + 20 offices in 14 self-sufficient country-organisations
• + 800 professionals at your service
• Only pan-EU solutions provider & system integrator
4 30/05/2012
5. Our Core Competences at a Glance
GOODS ID PEOPLE ID
(Pan-European) National & Supranational
Businesses Institutions / Governments
Enabling the Mobile
Enabling the Citizen
Worker
Security, G2C Process
Business Process
Improvements
Improvement
System Integration
Solution Building
Identification & Mobile
Technologies
5 30/05/2012
7. Business Challenges/Opportunities
Compliancy
with new recommendations (EFPIA / EC)
Harmonization of
pharmaceutical products
codification throughout Europe
via the implementation of a
serialised Datamatrix Code
(ECC200) on secondary
Serialisation packaging of all products
Datamatrix (prescription drugs) sold in
Europe
The checking of
pharmaceutical products at
their point of dispensing
(randomised serial numbers)
8. Business Challenges/Opportunities
Compliancy
with new regulations
Turkey: Datamatrix coding + serialisation since 2009
France: Datamatrix coding as of 01/01/2011
Impact on production lines of all
countries exporting to these
countries
9 30/05/2012
9. Business Challenges/Opportunities
Protection against
Counterfeit: unauthorized product introduced
into the legitimate distribution network
Theft: stolen from the legitimate distribution
network
Derivations: unauthorized sale of a product
based upon contractual restrictions (ex:
subcontractor manufacturer)
Track & Trace
Optimised treatments of claims en returns
Transparency towards 3rd parties
10 30/05/2012
10. The Solution - Requirements
Inspection
A total solution
Real-time coding
on high speed of barcode offering safe and smart
production lines quality integration of
hardware and
software
Secure storage
in DB
11 30/05/2012
11. Zetes’ offer: A complete solution
offering maximum security SEALING
TAMPER EVIDENT
INSPECTION
Protection against unauthorised opening
of secondary packaging during Datamatrix content
its transport
across the supply chain grade
Datamatrix
LABELLING
Tamper evident Text content
sealing High speed application
Consistency between Datamatrix and text
Application of pre-printed
Labelling MARKING/ CODING/ P&A
self-adhesive labels
Consistency Inspection data read and sent
between
E.g. social security requirements
Label position
High speed marking/coding/
print & apply onminutes
Up to 500 /
any production line
DB STORAGE
Marking/Coding/
Zetes Secure
Up to 500 units / minute
Serialisation management (guarantee uniqueness)
DB storage
Print & Apply solution Solid ERP integration
At any side required
Network management of print & control lines
12 30/05/2012
12. The Benefits
Working with HW partner of your
Open choice (Wolke, HP, Cognex, …)
Consistency of current
Solution installations
Up to 500p/minute
System Ensuring uptime
Performance of production Line
Flexibility In line with your specific
requirements
(Retrofit / no unnecessary investments
new system) required
19 30/05/2012
13. The Benefits
Analysis – Design – Development –
One-Stop- Implementation – Service &
Support from 1 single partner
Shop Peace of mind throughout
entire project
Auto-ID +25y System Integration
In house design & manufacturing
Expertise Proven solution, safe choice
+20 offices in 14 countries
Global Reach, Dedicated Competence Centre
Consistensy in multi-site/multi-
Local Service country projects, service & support
from local specialists
20 30/05/2012
14. What’s more…
End-to-end traceability solutions
Production line
environment
Datamatrix
Secondary Packaging Identification Box & Pallet Identification Order
Preparation/
Shipment
Verification/
Warehousing, (e)POD
Transport &
Logistics
environment
Moving/ Order Proof of
Goods Shipment
Replenish- Preparation Collection/
In/Out Verification
ment/Inventory Proof of
Delivery
21 30/05/2012
So Zetes offers solutions based on the identification of Goods and People and in both segments we try to do things differently and better than our competitors. How? Amongst others, by leveraging on a solid network of specialists and a great many years of experience. As you will see on the map, we are today present in 13 countries, 11 in Europe, and 2 in EMEA, i.e. Israel and Côte d’Ivoire (the CI office has been founded following the biometric passport project in Côte d’Ivoire and focuses entirely on this specific People ID activity). This pan-European presence is the result of 25 years of both organic growth and acquisitions. The company has originally been founded in Belgium in 1984 by Alain Wirtz, who is today still the CEO of the Group. Starting off in the barcode industry the company has continuously grown over the last 25 years, offering today a large solution portfolio based a wide variety of technologies, such as barcodes, voice recognition, RFID, printing, smart cards, biometrics etc. Since 2005 the company has been listed on the Euronext Stock Exchange. In the areas where we are not yet physically present, we work in partnership with local integrators. With our direct presence in Europe and network of more than 800 professionals, we hold a unique position in the market, as no other pan-European Auto-ID solution provider can offer a network of equal dimensions. In addition, to offer our international customers consistency in their solutions at international level, we have established strong partnerships with leading industry peers in Asia (Schmidt Electronics) and the USA (Peak).
Identification technologies such as barcoding, voice recognition, printing, RFID, smart cards, biometrics, etc., are at the heart of Zetes’ business. We use our knowledge of these technologies to design and integrate solutions that optimise various processes in many environments. On the one hand, our solutions will focus on the optimisation of business processes of mobile workers in and around the supply chain, typically by optimising accuracy, productivity, and efficiency. These types of solutions are typically used by commercial companies all over Europe and beyond. On the other hand, our expertise of technologies such as smart cards, biometrics, wireless infrastructure, etc. equally allow us to build our so-called People ID solutions, which are concentrated around optimising the capturing and managing data of citizens, voters, civilians etc. with the aim of optimising processes such as the organisation of elections, boarder control, government to citizen (G2C) processes such as tax on web etc. For these types of solutions Zetes works with national and supranational governments and institutions such as the United Nations.