Presentation Alliance of European Life Sciences Law Firms
(Julian Hitchcock and Sofie van der Meulen) on legal aspects of big data in pharma. Topics: privacy, IP, medical devices and IVD.
The document outlines various resources and programs available through the National Institutes of Health (NIH) to support research and development efforts, from early stage screening and validation to late stage clinical trials. It describes screening programs, technology characterization services, preclinical and clinical development resources across multiple NIH institutes focused on areas like cancer, neurodegeneration, infectious diseases, and more. The document encourages collaborations between NIH researchers and outside entities through licensing agreements, cooperative research agreements, and material transfers to help move technologies toward public health benefits.
Data Mining and Big Data Analytics in Pharma Ankur Khanna
The document proposes software solutions for drug research, including text mining, data warehousing, data mining, database development, and big data analytics. It discusses common challenges in drug research like the high costs and low success rates. It then describes various solutions like text mining patents and research to help identify new research opportunities and reduce duplication of efforts. It provides examples of how various pharmaceutical companies use data mining and warehousing techniques. Overall, the document pitches different IT solutions that can help pharmaceutical and life sciences companies address their research challenges and make their processes more efficient.
The document discusses the vision for data science at the National Institutes of Health (NIH). It outlines the goals of fostering an open ecosystem to enable biomedical research as a digital enterprise. Examples are provided of how precision medicine could benefit patients in the near future through large national research cohorts, improved understanding of diseases like diabetes through genomics, and new technologies. The document also discusses several key elements needed for the digital research enterprise, including communities, policies, infrastructure, and workforce training through initiatives like the Big Data to Knowledge program.
Disease Network is the science that has emerged to diagnose a disease from a network aspect
specifically. Networks are the group that interconnect to each others similarly disease networks are
the one that reveal concelled connection among apparently independent biomedical entities like
physiologic process, signaling receptors, in addition to genetic code, also they prove to exists
intitutive in addition to powerful way to learn/discover or diagnose a disease.Due to these networks,
we can now consume the elderly drugs and its method to learn/discover the new drug
accordingly.Example- Colchicine is used in gout but after repurposing it is also used in mediterranean
fever. This is because there are many factors that affect the body during mediterranean fever and
gout, we know that gout is a form of arthritis that causes pain in joints also mediterranean fever is the
one which is accompanied by pain in joints, therefore colchicine is used as a repurposed drug again.In
repurposing of medicines or drugs we first analyse the change in symptoms and identify the target
organ and accorgingly we produce a drug that is compatible with pharmacokinetics of the body. As
the availablity of transcriptomic,proteomic and metabolomic data sources are increasing day by day it helps in classification of disease .Also there are some networks reffered to as complex networks which can be called as collection of linked junctions/ nodes
BioIT 2017 - Ontoforce and Amgen Gene Knowledge DiscoveryWolfgang G. Hoeck
The document discusses a knowledge discovery platform called GKD that connects and aggregates internal and external research data to enable self-service knowledge discovery for scientists. Key points:
- GKD links different data sources together and allows data to be explored and discovered without barriers between systems.
- It provides a single access point for both private and public data about genes/targets through semantic integration and linking of data.
- Feedback from scientists highlights how GKD helps with various research activities like target identification and validation by bringing different types of relevant data within easy reach.
One Funder’s View for Advancing Open SciencePhilip Bourne
Robert Wood Johnson Foundation & SPARC Workshop on October 19, 2015 intended to catalyze a dialogue about opportunities for philanthropy and other funders in open access.
Presentation Alliance of European Life Sciences Law Firms
(Julian Hitchcock and Sofie van der Meulen) on legal aspects of big data in pharma. Topics: privacy, IP, medical devices and IVD.
The document outlines various resources and programs available through the National Institutes of Health (NIH) to support research and development efforts, from early stage screening and validation to late stage clinical trials. It describes screening programs, technology characterization services, preclinical and clinical development resources across multiple NIH institutes focused on areas like cancer, neurodegeneration, infectious diseases, and more. The document encourages collaborations between NIH researchers and outside entities through licensing agreements, cooperative research agreements, and material transfers to help move technologies toward public health benefits.
Data Mining and Big Data Analytics in Pharma Ankur Khanna
The document proposes software solutions for drug research, including text mining, data warehousing, data mining, database development, and big data analytics. It discusses common challenges in drug research like the high costs and low success rates. It then describes various solutions like text mining patents and research to help identify new research opportunities and reduce duplication of efforts. It provides examples of how various pharmaceutical companies use data mining and warehousing techniques. Overall, the document pitches different IT solutions that can help pharmaceutical and life sciences companies address their research challenges and make their processes more efficient.
The document discusses the vision for data science at the National Institutes of Health (NIH). It outlines the goals of fostering an open ecosystem to enable biomedical research as a digital enterprise. Examples are provided of how precision medicine could benefit patients in the near future through large national research cohorts, improved understanding of diseases like diabetes through genomics, and new technologies. The document also discusses several key elements needed for the digital research enterprise, including communities, policies, infrastructure, and workforce training through initiatives like the Big Data to Knowledge program.
Disease Network is the science that has emerged to diagnose a disease from a network aspect
specifically. Networks are the group that interconnect to each others similarly disease networks are
the one that reveal concelled connection among apparently independent biomedical entities like
physiologic process, signaling receptors, in addition to genetic code, also they prove to exists
intitutive in addition to powerful way to learn/discover or diagnose a disease.Due to these networks,
we can now consume the elderly drugs and its method to learn/discover the new drug
accordingly.Example- Colchicine is used in gout but after repurposing it is also used in mediterranean
fever. This is because there are many factors that affect the body during mediterranean fever and
gout, we know that gout is a form of arthritis that causes pain in joints also mediterranean fever is the
one which is accompanied by pain in joints, therefore colchicine is used as a repurposed drug again.In
repurposing of medicines or drugs we first analyse the change in symptoms and identify the target
organ and accorgingly we produce a drug that is compatible with pharmacokinetics of the body. As
the availablity of transcriptomic,proteomic and metabolomic data sources are increasing day by day it helps in classification of disease .Also there are some networks reffered to as complex networks which can be called as collection of linked junctions/ nodes
BioIT 2017 - Ontoforce and Amgen Gene Knowledge DiscoveryWolfgang G. Hoeck
The document discusses a knowledge discovery platform called GKD that connects and aggregates internal and external research data to enable self-service knowledge discovery for scientists. Key points:
- GKD links different data sources together and allows data to be explored and discovered without barriers between systems.
- It provides a single access point for both private and public data about genes/targets through semantic integration and linking of data.
- Feedback from scientists highlights how GKD helps with various research activities like target identification and validation by bringing different types of relevant data within easy reach.
One Funder’s View for Advancing Open SciencePhilip Bourne
Robert Wood Johnson Foundation & SPARC Workshop on October 19, 2015 intended to catalyze a dialogue about opportunities for philanthropy and other funders in open access.
This document provides information about the "Big Data & Analytics for Pharma Summit" event taking place on November 3-4, 2016 in Philadelphia. The event will focus on challenges in pharmaceutical R&D, drug development, and safety monitoring, and how analytics can help address these challenges in an evolving market focused on patient-centricity. Key themes include real-world data usage, marketing, business models, decision making, and drug research. The agenda includes keynote speakers from major pharmaceutical companies discussing various analytics applications and case studies.
dkNET Webinar: Creating and Sustaining a FAIR Biomedical Data Ecosystem 10/09...dkNET
Abstract
In this presentation, Susan Gregurick, Ph.D., Associate Director of Data Science and Director, Office of Data Science Strategy at the National Institutes of Health, will share the NIH’s vision for a modernized, integrated FAIR biomedical data ecosystem and the strategic roadmap that NIH is following to achieve this vision. Dr. Gregurick will highlight projects being implemented by team members across the NIH’s 27 institutes and centers and will ways that industry, academia, and other communities can help NIH enable a FAIR data ecosystem. Finally, she will weave in how this strategy is being leveraged to address the COVID-19 pandemic.
Presenter: Susan Gregurick, Ph.D., Associate Director of Data Science and Director, Office of Data Science Strategy at the National Institutes of Health
dkNET Webinar Information: https://dknet.org/about/webinar
This document discusses how big data can help reduce costs and increase productivity in drug R&D. It outlines challenges such as increased clinical trials, patients, and data requirements that have led to higher R&D costs. Big data is presented as a solution by bringing more insights from data rather than resources. The document provides case studies and a 6-step approach for companies to leverage big data in R&D, including establishing an analytics strategy, identifying relevant data sources, and optimizing their analytics organization.
Clinical Research Informatics World 2015Jaime Hodges
The document provides information about the "Clinical Research Informatics World 2015" conference to be held on May 6-7, 2015 in Boston, MA. It includes details about keynote speakers, sessions, sponsors and registration. The conference will focus on topics such as leveraging new technologies and analytics to advance clinical trials, using existing data sources to support trials, and cross-industry data sharing. Sessions will provide case studies and discuss strategies for areas like establishing big data strategies, bringing patient centricity to trials, and innovating clinical trial processes with new technologies.
This document discusses ways to help advance research for rare and orphan diseases through open collaboration and data sharing. It provides examples of how collaborative platforms and tools can help organizations with limited resources pool data and expertise. Specifically, it describes a secure web-based platform that allows private and public data to be simultaneously searched to facilitate partnerships across various sectors.
Pistoia Alliance datathon for drug repurposing for rare diseasesPistoia Alliance
This document provides information about a datathon focused on drug repurposing for rare diseases. It discusses:
1) The goals of the datathon to use data science approaches like machine learning to identify potential drug repurposing opportunities for rare diseases.
2) The partners involved - The Pistoia Alliance, Cures Within Reach, and Mission: Cure.
3) How participants can access data on the Entellect platform and work collaboratively on the datathon challenge to find new treatments for rare diseases.
CureMatch is developing a software tool to help cancer doctors choose treatment options for their patients. The software combines data from multiple sources to suggest personalized drug combinations for individual cancer patients. It aims to move cancer treatment towards precision medicine by providing data-driven guidance to physicians. CureMatch was founded in 2015 and is based in San Diego. It has 5 employees and funding from investor Analytics Ventures. The company's software analyzes genetic and diagnostic information about a patient's cancer to recommend potential drug combinations, and it will become more accurate as doctors add treatment outcomes to the database.
This document discusses Sage Bionetworks, a non-profit organization that pilots components to build an open and collaborative biomedical research commons. It describes several consortia and projects Sage supports that involve data sharing and collaborative research across disciplines. It also discusses the mPower mobile health study for Parkinson's disease research and efforts to promote an open ecosystem where research is conducted for others to consume and analyze while balancing privacy and oversight.
Healthcare Conference 2013 : Genes, Clouds and Cancer - dr. Andrew LittD3 Consutling
Dell Healthcare provides IT services to healthcare organizations worldwide. They serve over 50% of US hospitals, the top 10 pharmaceutical companies, and 100 insurance organizations. Dell Healthcare manages billions of medical images in the cloud, billions of security events daily, and provides genomic sequencing services. They are sponsoring the first FDA-approved clinical trial using whole genome sequencing to provide personalized cancer treatment to children with neuroblastoma. The trial aims to reduce analysis time from weeks to hours using Dell's high performance computing capabilities and improve collaboration using their genomics cloud. The goal is to expand personalized medicine from treating a few children to hundreds and thousands.
biomedical research in an increasingly digital worldBrian Bot
Sage Bionetworks is a non-profit organization that supports open and collaborative biomedical research across organizations through various consortiums and partnerships. Some of its initiatives include the TCGA Pan-Cancer Consortium involving analysis of 12 tumor types, the CommonMind Consortium involving collection and analysis of brain tissue samples for schizophrenia research, and the Accelerating Medicines Partnership, a public-private partnership focused on diseases such as Alzheimer's. Sage Bionetworks also supports data challenges and the development of collaborative research platforms.
NIH Drug Discovery and Development - NCTT and CTSAsCTSI at UCSF
Presented at the UC Braid Retreat: Imagine a statewide research engine of pooled resources, data, and expertise that accelerates the “translation” of academic research to direct patient benefit. That's the goal of the University of California Biomedical Research Acceleration, Integration, and Development (UC BRAID) program.
Advanced Analytics for Clinical Data Full Event GuidePfizer
This document provides information about the "Advanced Analytics for Clinical Data" conference to be held February 1-2, 2017 in San Francisco. The conference will focus on applying advanced analytics and data-driven methodologies in clinical research and drug development. It will feature presentations from experts in clinical data science from major pharmaceutical companies. Topics will include implementing analytics from areas like biostatistics, omics, and wearables. Attendees will learn how to extract value from large datasets and new sources of data. The agenda also includes panels on leveraging big data in clinical trials and evolving the role of clinical data management.
1. Collaboration and data sharing in science is essential but requires technological and cultural changes to allow for analysis and insights.
2. Improving data sharing across organizations is challenging due to heterogeneous systems and social barriers.
3. The Medicines Discovery Catapult is supporting the biopharma sector by developing solutions to improve data interpretation, collaborative data sharing between organizations, and by matching industry challenges to technology providers.
SMi Group's AI in Drug Discovery 2020 conferenceDale Butler
This document provides information about an upcoming conference on AI in Drug Discovery taking place from March 16-17, 2020 in London, UK. It includes details about the program, speakers, registration fees and deadlines. The conference will explore how machine learning and AI are being applied across the drug discovery process, from compound design and virtual screening to toxicity prediction. There will be case studies presented from major pharmaceutical companies on their experience integrating AI. The document also advertises sponsorship opportunities for the event.
This document discusses challenges and opportunities in the pharmaceutical industry. It notes that R&D costs are high due to extensive outsourcing, and benchmarking outsourced R&D units could lower costs by 40%. It also describes a software tool called PAT that would help predict side effects and check patent uniqueness of new drug formulas, saving 40% of time wasted on failed experiments. Overall the document analyzes ways to improve innovation and lower costs in pharmaceutical R&D through analytical solutions.
Slides from CDD's March 22 Webinar - Penetrating Gram Negative Bacteria. Hosted by Brad Sherborne (Merck) featuring Derek Tan (Memorial Sloan Kettering Cancer Center) and Helen Zgurskaya (University of Oklahoma).
Open Drug Discovery Teams Feature OverviewAlex Clark
This document describes Open Drug Discovery Teams (ODDT), a free mobile app for iOS devices that aggregates open chemistry data from various sources. ODDT allows users to browse topics like rare diseases, endorse or comment on entries, and view chemical structures and reactions. Future developments may include more topics, data sources, and advanced cheminformatics tools. The goal is to facilitate collaboration in open drug discovery and chemistry.
Clinical Research Informatics Year-in-ReviewPeter Embi
Peter Embi's 2018 Clinical Research Informatics Year-in-Review. Presented as closing Keynote address at the 2018 AMIA Informatics Summit in San Francisco, CA.
2015-02-10 The Open PHACTS Discovery Platform: Semantic Data Integration for ...open_phacts
The Open PHACTS Discovery Platform integrates multiple biomedical data resources into a single open access point using semantic web technology. It is guided by business questions from pharmaceutical companies to integrate data from sources like ChEMBL, DrugBank, UniProt, and more. The platform is run as a public-private partnership through 2021 to support drug discovery.
After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success.
This document provides information about the "Big Data & Analytics for Pharma Summit" event taking place on November 3-4, 2016 in Philadelphia. The event will focus on challenges in pharmaceutical R&D, drug development, and safety monitoring, and how analytics can help address these challenges in an evolving market focused on patient-centricity. Key themes include real-world data usage, marketing, business models, decision making, and drug research. The agenda includes keynote speakers from major pharmaceutical companies discussing various analytics applications and case studies.
dkNET Webinar: Creating and Sustaining a FAIR Biomedical Data Ecosystem 10/09...dkNET
Abstract
In this presentation, Susan Gregurick, Ph.D., Associate Director of Data Science and Director, Office of Data Science Strategy at the National Institutes of Health, will share the NIH’s vision for a modernized, integrated FAIR biomedical data ecosystem and the strategic roadmap that NIH is following to achieve this vision. Dr. Gregurick will highlight projects being implemented by team members across the NIH’s 27 institutes and centers and will ways that industry, academia, and other communities can help NIH enable a FAIR data ecosystem. Finally, she will weave in how this strategy is being leveraged to address the COVID-19 pandemic.
Presenter: Susan Gregurick, Ph.D., Associate Director of Data Science and Director, Office of Data Science Strategy at the National Institutes of Health
dkNET Webinar Information: https://dknet.org/about/webinar
This document discusses how big data can help reduce costs and increase productivity in drug R&D. It outlines challenges such as increased clinical trials, patients, and data requirements that have led to higher R&D costs. Big data is presented as a solution by bringing more insights from data rather than resources. The document provides case studies and a 6-step approach for companies to leverage big data in R&D, including establishing an analytics strategy, identifying relevant data sources, and optimizing their analytics organization.
Clinical Research Informatics World 2015Jaime Hodges
The document provides information about the "Clinical Research Informatics World 2015" conference to be held on May 6-7, 2015 in Boston, MA. It includes details about keynote speakers, sessions, sponsors and registration. The conference will focus on topics such as leveraging new technologies and analytics to advance clinical trials, using existing data sources to support trials, and cross-industry data sharing. Sessions will provide case studies and discuss strategies for areas like establishing big data strategies, bringing patient centricity to trials, and innovating clinical trial processes with new technologies.
This document discusses ways to help advance research for rare and orphan diseases through open collaboration and data sharing. It provides examples of how collaborative platforms and tools can help organizations with limited resources pool data and expertise. Specifically, it describes a secure web-based platform that allows private and public data to be simultaneously searched to facilitate partnerships across various sectors.
Pistoia Alliance datathon for drug repurposing for rare diseasesPistoia Alliance
This document provides information about a datathon focused on drug repurposing for rare diseases. It discusses:
1) The goals of the datathon to use data science approaches like machine learning to identify potential drug repurposing opportunities for rare diseases.
2) The partners involved - The Pistoia Alliance, Cures Within Reach, and Mission: Cure.
3) How participants can access data on the Entellect platform and work collaboratively on the datathon challenge to find new treatments for rare diseases.
CureMatch is developing a software tool to help cancer doctors choose treatment options for their patients. The software combines data from multiple sources to suggest personalized drug combinations for individual cancer patients. It aims to move cancer treatment towards precision medicine by providing data-driven guidance to physicians. CureMatch was founded in 2015 and is based in San Diego. It has 5 employees and funding from investor Analytics Ventures. The company's software analyzes genetic and diagnostic information about a patient's cancer to recommend potential drug combinations, and it will become more accurate as doctors add treatment outcomes to the database.
This document discusses Sage Bionetworks, a non-profit organization that pilots components to build an open and collaborative biomedical research commons. It describes several consortia and projects Sage supports that involve data sharing and collaborative research across disciplines. It also discusses the mPower mobile health study for Parkinson's disease research and efforts to promote an open ecosystem where research is conducted for others to consume and analyze while balancing privacy and oversight.
Healthcare Conference 2013 : Genes, Clouds and Cancer - dr. Andrew LittD3 Consutling
Dell Healthcare provides IT services to healthcare organizations worldwide. They serve over 50% of US hospitals, the top 10 pharmaceutical companies, and 100 insurance organizations. Dell Healthcare manages billions of medical images in the cloud, billions of security events daily, and provides genomic sequencing services. They are sponsoring the first FDA-approved clinical trial using whole genome sequencing to provide personalized cancer treatment to children with neuroblastoma. The trial aims to reduce analysis time from weeks to hours using Dell's high performance computing capabilities and improve collaboration using their genomics cloud. The goal is to expand personalized medicine from treating a few children to hundreds and thousands.
biomedical research in an increasingly digital worldBrian Bot
Sage Bionetworks is a non-profit organization that supports open and collaborative biomedical research across organizations through various consortiums and partnerships. Some of its initiatives include the TCGA Pan-Cancer Consortium involving analysis of 12 tumor types, the CommonMind Consortium involving collection and analysis of brain tissue samples for schizophrenia research, and the Accelerating Medicines Partnership, a public-private partnership focused on diseases such as Alzheimer's. Sage Bionetworks also supports data challenges and the development of collaborative research platforms.
NIH Drug Discovery and Development - NCTT and CTSAsCTSI at UCSF
Presented at the UC Braid Retreat: Imagine a statewide research engine of pooled resources, data, and expertise that accelerates the “translation” of academic research to direct patient benefit. That's the goal of the University of California Biomedical Research Acceleration, Integration, and Development (UC BRAID) program.
Advanced Analytics for Clinical Data Full Event GuidePfizer
This document provides information about the "Advanced Analytics for Clinical Data" conference to be held February 1-2, 2017 in San Francisco. The conference will focus on applying advanced analytics and data-driven methodologies in clinical research and drug development. It will feature presentations from experts in clinical data science from major pharmaceutical companies. Topics will include implementing analytics from areas like biostatistics, omics, and wearables. Attendees will learn how to extract value from large datasets and new sources of data. The agenda also includes panels on leveraging big data in clinical trials and evolving the role of clinical data management.
1. Collaboration and data sharing in science is essential but requires technological and cultural changes to allow for analysis and insights.
2. Improving data sharing across organizations is challenging due to heterogeneous systems and social barriers.
3. The Medicines Discovery Catapult is supporting the biopharma sector by developing solutions to improve data interpretation, collaborative data sharing between organizations, and by matching industry challenges to technology providers.
SMi Group's AI in Drug Discovery 2020 conferenceDale Butler
This document provides information about an upcoming conference on AI in Drug Discovery taking place from March 16-17, 2020 in London, UK. It includes details about the program, speakers, registration fees and deadlines. The conference will explore how machine learning and AI are being applied across the drug discovery process, from compound design and virtual screening to toxicity prediction. There will be case studies presented from major pharmaceutical companies on their experience integrating AI. The document also advertises sponsorship opportunities for the event.
This document discusses challenges and opportunities in the pharmaceutical industry. It notes that R&D costs are high due to extensive outsourcing, and benchmarking outsourced R&D units could lower costs by 40%. It also describes a software tool called PAT that would help predict side effects and check patent uniqueness of new drug formulas, saving 40% of time wasted on failed experiments. Overall the document analyzes ways to improve innovation and lower costs in pharmaceutical R&D through analytical solutions.
Slides from CDD's March 22 Webinar - Penetrating Gram Negative Bacteria. Hosted by Brad Sherborne (Merck) featuring Derek Tan (Memorial Sloan Kettering Cancer Center) and Helen Zgurskaya (University of Oklahoma).
Open Drug Discovery Teams Feature OverviewAlex Clark
This document describes Open Drug Discovery Teams (ODDT), a free mobile app for iOS devices that aggregates open chemistry data from various sources. ODDT allows users to browse topics like rare diseases, endorse or comment on entries, and view chemical structures and reactions. Future developments may include more topics, data sources, and advanced cheminformatics tools. The goal is to facilitate collaboration in open drug discovery and chemistry.
Clinical Research Informatics Year-in-ReviewPeter Embi
Peter Embi's 2018 Clinical Research Informatics Year-in-Review. Presented as closing Keynote address at the 2018 AMIA Informatics Summit in San Francisco, CA.
2015-02-10 The Open PHACTS Discovery Platform: Semantic Data Integration for ...open_phacts
The Open PHACTS Discovery Platform integrates multiple biomedical data resources into a single open access point using semantic web technology. It is guided by business questions from pharmaceutical companies to integrate data from sources like ChEMBL, DrugBank, UniProt, and more. The platform is run as a public-private partnership through 2021 to support drug discovery.
After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success.
This document provides a summary of A.P.S Saini's qualifications and experience. Saini has a Master's degree in Electrical and Computer Engineering and over 1 year of experience as a Telecommunications Engineer. Key skills include networking, routing protocols, IP telephony, fiber optics, wireless communications, and hardware and software programming languages. Relevant experience includes engineering internships at Scope Telecomm and Havells India, where duties involved monitoring networks, troubleshooting issues, and assisting with telecom systems and circuit breaker installation and testing. Projects highlight design and simulation experience with communication systems and protocols using tools like MATLAB, Qualnet, Optisystem, and hardware verification using SystemVerilog and formal verification tools.
This poster analysis compares two horror movie posters that feature a moth. Both posters place the character in the center with a moth. While the first poster features a woman with angelic features and red eyes, the second has a man with a rough, worn appearance and red eyes. This suggests the characters have two conflicting personalities - one gentle and the other evil. The red eyes in both posters link the characters and imply they are alike despite their different appearances. One poster provides more information typically found in film posters while the other is a simpler teaser design.
The document discusses various types of slim and lightweight laptops, including bargain slim line laptops from auctions and sales. It also mentions slim line DVD combos and burners that can be used with laptops from brands like Dell, Acer, Sony, and others.
This document provides project details for the rehabilitation of Main Street from Route 1 to just west of Railroad Avenue in Biddeford, Maine. It includes a title sheet, typical road sections, estimated quantities, and general notes. The project will repair and resurface the existing roadway with hot mix asphalt and includes sidewalk and drainage improvements. Estimated quantities of excavation, base materials, pavement, and other items are provided for two rehabilitation options. General notes specify construction requirements and responsibilities.
This document discusses supply chain management. It defines a supply chain as involving two or more parties linked by the flow of materials, information, and money to fulfill customer requests. Supply chain management aims to get the right goods to the right place at the right time while maximizing total value. It encompasses logistics and focuses on managing the flow of items, information, cash, and ideas through coordination across the supply chain. The document also outlines the primary cycles in a supply chain process between suppliers, manufacturers, distributors, and customers.
Este documento describe los aspectos que deben evaluarse en una Planeación didáctica argumentada, incluyendo los aprendizajes esperados por grado, un escrito de reflexión basado en los aprendizajes esperados, y detalles sobre la elaboración de la planeación como el contexto escolar, diagnóstico del grupo, plan de clase, estrategias de enseñanza y evaluación. También explica que los maestros de primaria deberán diseñar una Planeación didáctica argumentada en cuatro horas durante su evaluación, basándose en un aprendiz
The document provides details of a marketing campaign for the World Wildlife Fund (WWF). It includes a situational analysis, SWOT analysis, analysis of competitors like Greenpeace and Humane Society International, identification of key product benefits of WWF, description of the target audience and big idea for the campaign. Media recommendations include TV, radio, print and digital advertisements to raise awareness about climate change and encourage actions among working adults aged 25-40 in Singapore. The total proposed media budget is $150,000.
Powering Scientific Discovery with the Semantic Web (VanBUG 2014)Michel Dumontier
The document discusses how the semantic web can help power scientific discovery. It proposes building a massive network of interconnected data and software using web standards to 1) generate and test hypotheses by discovering associations in the data, 2) gather evidence to support or dispute hypotheses, and 3) contribute new knowledge back to the global network. This network, called the semantic web, treats data as a web of facts that can be shared and queried using semantic web standards. The document provides examples of how linked open data in the life sciences is being created and used via semantic web technologies to integrate data from multiple sources and answer complex queries.
Identifying Drug Interaction Candidates in Real-World DataNeo4j
The document describes the Real-world Evidence Drug-Drug Interaction (REDDI) Match project. It introduces the multidisciplinary team developing the solution. REDDI Match analyzes real-world data to identify potential drug-drug interactions, including for off-label drug uses like chloroquine for COVID-19. It represents prescription data as a graph to efficiently identify interaction patterns. The team detects communities in the graph and explores interactions within those contexts. A demo of the system is provided with notes on potential future enhancements.
The FDA Digital Health Center of Excellence and the Advancement of Digital He...Greenlight Guru
The FDA Digital Health Center of Excellence is part of the planned evolution of the digital health program with the intent to drive synergy for digital health efforts, align strategy with implementation, prepare the FDA for the digital health future, and protect patients and maintain the FDA standards of safety and effectiveness.
Ultimately, the program works to strategically advance science and evidence for digital health technologies that meets the needs of
stakeholders.
This free in-depth webinar, presented by Matthew DiamondChief Medical Officer, Digital Health Center of Excellence, will cover the digital health landscape and areas of application, goals and outcomes, planned services and launch plan, and the current areas of focus - including AI/ML-Based SaMD.
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
Big Data and its Impact on Industry (Example of the Pharmaceutical Industry)Hellmuth Broda
While we bemoan the ever increasing data tsunami new technologies allow to harvest the gold nuggets in the hay stack.
Using the example of the Pharmaceutical Industry some of the possible business uses for Big Data Analitics are outlined.
The document advertises the Big Data Leaders Forum 2015 conference on big data and eHealth in clinical development. The two-day conference will be held on October 7-8, 2015 in Washington, DC and feature over 80 speakers from pharmaceutical companies, biotechs, payers, CROs, government, and academia. Attendees will include senior decision makers from various stakeholders looking for big data and eHealth solutions. Sessions will address using big data to inform clinical trial design, commercial and payer strategies, and precision medicine. The conference provides an opportunity to network with leaders across industries.
The document advertises the Big Data Leaders Forum 2015 conference on big data and eHealth in clinical development. The two-day conference will be held on October 7-8, 2015 in Washington, DC and feature over 80 speakers from pharmaceutical companies, biotechs, payers, CROs, government, and academia. Attendees will learn about how big data and eHealth technologies can inform clinical trial design, generate real-world evidence, support commercial and payer strategies, and enable precision medicine. Sessions will explore using data from sources like EHRs, mobile technologies, wearables, social media, and patient-reported outcomes to enrich drug development and improve patient outcomes.
Harnessing Edge Informatics to Accelerate Collaboration in BioPharma (Bio-IT ...Tom Plasterer
As scientists in the life sciences we are trained to pursue singular goals around a publication or a validated target or a drug submission. Our failure rates are exceedingly high especially as we move closer to patients in the attempt to collect sufficient clinical evidence to demonstrate the value of novel therapeutics. This wastes resources as well as time for patients depending upon us for the next breakthrough.
Edge Informatics is an approach to ameliorate these failures. Using both technical and social solutions together knowledge can be shared and leveraged across the drug development process. This is accomplished by making data assets discoverable, accessible, self-described, reusable and annotatable. The Open PHACTS project pioneered this approach and has provided a number of the technical and social solutions to enable Edge Informatics. A number of pre-competitive consortia and some content providers have also embraced this approach, facilitating networks of collaborators within and outside a given organization. When taken together more accurate, timely and inclusive decision-making is fostered.
The document provides information about an upcoming conference on clinical data disclosure and transparency taking place on January 28-29, 2015 in Philadelphia, PA. It lists the conference sponsors and over 30 speakers from 20+ companies that will discuss approaches to data sharing and ensuring compliance with regulations. Attendees will include chief medical officers, general counsels, and clinical professionals involved in disclosure, clinical operations, and regulatory affairs. The conference will explore implications of increased transparency requirements and navigating public disclosure on platforms like ClinicalTrials.gov and EudraCT.
Interactive Business Intelligence for Big Data in Life SciencesPerficient, Inc.
Visual. Dynamic. Flexible. The ability to make intelligent business and clinical decisions faster is what life sciences companies want from business intelligence (BI) solutions. That's why pharmaceuticals, medical device companies, and CROs use data visualization technologies that work with a multitude of data sources across various organizational departments.
In our webinar, Perficient’s Andre Serafini, Senior Solutions Architect, discussed how you, too, can leverage analytics and reporting applications to support your BI needs. He used a cutting edge BI tool to perform several live demonstrations of real-life applications in the life sciences industry.
See how interactive, real-time BI and analytics on Big Data can be a valuable asset for your organization’s clinical, pharmacovigilance, and sales operations.
Big data plays an important role in promoting emerging scientific and interdisciplinary research by enabling decision-making. However, in order to provide actionable insights relevant for the support of decision-making, several challenges for data management, analytics, and knowledge discovery need to be addressed. In this talk, we will describe a knowledge-driven approach capable to ingest Big data sources and integrate them into a knowledge graph that represents not only the meaning of the entities published by these data sources, but also that provides the basis for the discovery of unknown patterns and associations between these entities. The features of this knowledge-driven framework are shown in the context of the EU funded project iASiS (http://project-iasis.eu/) , where it is used to pave the way for personalized diagnosis and treatments
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This document advertises and provides an agenda for the "Data Quality & Technology in Clinical Trials 2016" conference to be held in Philadelphia on April 18-19, 2016. The conference will focus on how pharmaceutical companies can maximize data quality, become data-driven organizations, and harness analytics to improve clinical trial design, monitoring, and outcomes. Speakers will include executives from major pharmaceutical companies as well as regulators and discuss topics like unlocking value from clinical trial data, using patient-generated data, and harnessing new technologies in clinical trials. The goal is to help pharmaceutical companies transition to being data-driven organizations and improve clinical development timelines and success rates through better data practices and technologies.
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Online communities and social networks like Twitter and Facebook have become important real-world data repositories that can be leveraged by life sciences organizations to gain insight into the patient experience, as well as to identify potential safety issues related to drugs and devices – otherwise known as safety signal detection.
Perficient’s director of safety and pharmacovigilance, Dr. Rodney Lemery, discussed the methods, benefits, and challenges involved with mining real-world data for adverse event drug reactions and other safety signals.
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Edge Informatics is an approach to accelerate collaboration in the BioPharma pipeline. By combining technical and social solutions knowledge can be shared and leveraged across the multiple internal and external silos participating in the drug development process. This is accomplished by making data assets findable, accessible, interoperable and reusable (FAIR). Public consortia and internal efforts embracing FAIR data and Edge Informatics are highlighted, in both preclinical and clinical domains.
This talk was presented at the Molecular Medicine Tri-Conference in San Francisco, CA on February 20, 2017
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The document discusses Strand Genomics Inc., which offers genomic analysis and clinical interpretation software and services. It focuses on personalized medicine by using its StrandOmics platform to analyze genomic data and determine disease risks for individuals. StrandOmics aims to make genomic testing routine in medical care to help clinicians make more informed decisions. Strand has grown to over 200 scientists and serves over 2,000 labs and 100,000 patients. Its partnership with Health Care Global Enterprises successfully piloted cancer risk assessment and molecular diagnosis for over 50 patients in India.
CORD Rare Drug Conference, June 8 - 9, 2022
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• AI for Data Management and Enhancement: Aaron Leibtag, Pentavere
• Patient Support and RWE: Laurie Lambert, CADTH
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CDD aids collaborations by revealing known drugs that can reverse chloroquine resistance. CDD has successfully built collaborative drug discovery communities with thousands of engaged scientists. The CDD platform includes secure vaults for private data sharing, modules for collaborating by selectively sharing data subsets, and public datasets from community members and vendors.
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White & Case Digital Health: Rethinking Healthcare in a
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The document discusses breaking down information silos by promoting information sharing and collaboration. It describes how information silos are caused by rigid technologies, legacy processes, and lack of incentives for collaboration. This limits productivity, innovation, and collaboration. The document proposes providing technologies and processes that support information sharing, integrating data through standards, and building a collaborative culture with mutual trust. It provides examples of public-private partnerships between organizations like NIH, FDA, and companies to analyze clinical trial data and stimulate further research.
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This webinar discusses workflow tools to support life science research. It includes presentations on the Common Workflow Language (CWL) by Michael Crusoe and uses of Knime and Pipeline Pilot workflows with Open PHACTS examples. There will also be a panel discussion on the future of workflows for life science research with speakers from Eli Lilly, Janssen, and others. Example CWL workflows are shown to demonstrate portable life science workflows.
Open PHACTS provides a single access point for integrating multiple biomedical data resources. It has transitioned from an EU project to the Open PHACTS Foundation to sustain the platform long-term. Challenges included addressing licensing issues across different data sources and enabling maximum dissemination. Usage has grown to over 500 million queries. The Foundation is pursuing collaboration, grants, and industry partnerships to support ongoing development and new projects. It welcomes contributions to improve services and develop new data and workflows.
Open PHACTS Webinar: Computational Protocols for In Silico Target Validationopen_phacts
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Combination Therapies
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Chemotherapy
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Open PHACTS webinar June 2016 - Data2Discovery
1. DATA2DISCOVERY
OpenPHACTS:
Maximizing Impact for
Pharmaceutical Applications
DAVID WILD, PhD.
CEO Data2Discovery Inc
Associate Professor and Director of Data Science, Indiana University
http://d2discovery.com - http://djwild.info - david@d2discovery.com
DATA SCIENCE DATA2DISCOVERY
1