As a novel solution to aggregate data within and across multiple trials, Xcellerate Clinical Data Hub helps standardize current operational and clinical data that feed into the Xcellerate Informatics Suite.
Xcellerate Data Review allows data managers to detect instances and sources of missing data, high query rates, delayed data entry and other data quality issues that impact trial data integrity.
Late Binding in Data Warehouses: Desiging for Analytic AgilityHealth Catalyst
Listen to Part 2 of the Late-Binding (TM) Data Warehouse webinar, a separate webinar focused on answering detailed follow-up questions generated from the first Late-Binding (TM) Data Warehouse webinar.
Seattle Code Camp 2016- Role of Data Science in HHealthcareRuba Qaqish
Everyone loves to shake a stick at the healthcare industry for being backward. The fact is that there is no lack of technology or data in healthcare. The biggest challenge for healthcare providers is to identify what questions to ask the data. My team has implemented over 75 enterprise data warehouse projects in the US healthcare industry.
This talk shares some of the examples of how data is used in the healthcare industry for compliance reporting (BI) and predictive analytics.
At the end, I will also share some ideas on what questions to ask from healthcare data. Some of these ideas are now products built by industry leaders like Caradigm, GE Healthcare, Get:Well Network and Philips Healthcare.
Perhaps, you will be inspired to build the next game changing product for the healthcare industry!
HySynth Clinical Data Repository is used for storing, integrating ,managing and reporting on clinical studies.
It enables pooling of clinical and nonclinical data from multiple sources into a single environment. Better regulatory compliance with comprehensive security, an audit trail, and traceability, More-informed decision-making through pooling and analysis of clinical and nonclinical data
CDR has been developed to revolutionize ability to:
- Address complex health authority questions quickly and completely
- Produce CDISC compliant submissions
- Review safety data in real-time, mine our overall database for scientific and commercial queries
At HySynth provide,
- Business case development and cost analysis
- Requirements and design management
- Best practice analysis and recommendations
- Installation and configuration
- Oracle CDA and LSH pilots and proofs of concept
- Hosting
- Oracle CDA and LSH implementation
- CDA and LSH validation
- CDA and LSH training
- CDA and LSH extension development
LST on the following applications
- Argus Safety Suite
- Oracle Clinical / Remote Data Capture (RDC) /
- Thesaurus Management System (TMS)
- Oracle Inform EDC / Central Designer / Central Coding
- Life Sciences Data Hub (LSH)
- Oracle Data Management Workbench (DMW)
- Oracle Clinical Development Analytics (CDA)
- Adverse Event Reporting System (AERS)
- SAS
As a novel solution to aggregate data within and across multiple trials, Xcellerate Clinical Data Hub helps standardize current operational and clinical data that feed into the Xcellerate Informatics Suite.
Xcellerate Data Review allows data managers to detect instances and sources of missing data, high query rates, delayed data entry and other data quality issues that impact trial data integrity.
Late Binding in Data Warehouses: Desiging for Analytic AgilityHealth Catalyst
Listen to Part 2 of the Late-Binding (TM) Data Warehouse webinar, a separate webinar focused on answering detailed follow-up questions generated from the first Late-Binding (TM) Data Warehouse webinar.
Seattle Code Camp 2016- Role of Data Science in HHealthcareRuba Qaqish
Everyone loves to shake a stick at the healthcare industry for being backward. The fact is that there is no lack of technology or data in healthcare. The biggest challenge for healthcare providers is to identify what questions to ask the data. My team has implemented over 75 enterprise data warehouse projects in the US healthcare industry.
This talk shares some of the examples of how data is used in the healthcare industry for compliance reporting (BI) and predictive analytics.
At the end, I will also share some ideas on what questions to ask from healthcare data. Some of these ideas are now products built by industry leaders like Caradigm, GE Healthcare, Get:Well Network and Philips Healthcare.
Perhaps, you will be inspired to build the next game changing product for the healthcare industry!
HySynth Clinical Data Repository is used for storing, integrating ,managing and reporting on clinical studies.
It enables pooling of clinical and nonclinical data from multiple sources into a single environment. Better regulatory compliance with comprehensive security, an audit trail, and traceability, More-informed decision-making through pooling and analysis of clinical and nonclinical data
CDR has been developed to revolutionize ability to:
- Address complex health authority questions quickly and completely
- Produce CDISC compliant submissions
- Review safety data in real-time, mine our overall database for scientific and commercial queries
At HySynth provide,
- Business case development and cost analysis
- Requirements and design management
- Best practice analysis and recommendations
- Installation and configuration
- Oracle CDA and LSH pilots and proofs of concept
- Hosting
- Oracle CDA and LSH implementation
- CDA and LSH validation
- CDA and LSH training
- CDA and LSH extension development
LST on the following applications
- Argus Safety Suite
- Oracle Clinical / Remote Data Capture (RDC) /
- Thesaurus Management System (TMS)
- Oracle Inform EDC / Central Designer / Central Coding
- Life Sciences Data Hub (LSH)
- Oracle Data Management Workbench (DMW)
- Oracle Clinical Development Analytics (CDA)
- Adverse Event Reporting System (AERS)
- SAS
Strokepad is a comprehensive, real-time, point-of-care digital clinical record specifically designed for stroke patients, encompassing the entire management pathway from admission to discharge.
It is a highly optimized, digital tablet interface with 'pen and paper' functionality, eliminating the need for dual entry or the use of parallel paper records throughout the care pathway.
Strokepad contains a built-in data field management which optimizes the collection of clinical and managerial data, reducing revenue loss through inaccurate coding.
Strokepad fully automates the processing of outcome data which eliminates resource intensive duplicate data collection for reporting and audit.ion of clinical and managerial data, reducing revenue loss through inaccurate coding.
The fundamental source of cost and error is in duplication:
^The clinician or nurse inputs the patients data directly into StrokePad at the bedside
^No duplication
^No data misunderstandings
^No duplicate recordings
^Reduced costs
^Reduced errors
More time for patient care
mHealth Israel_Ben Echeazu_Highmark Health_ Startups Engaging with US PayersLevi Shapiro
Presentation by Ben Echeaz, Business Development Director, Highmark Health, March 25, 2019, for the mHealth Israel community: Startups Engaging with US Payers. Includes overview of the US Payerand health insurance sector, Relationship to Blue Cross Blue Shield, Challenges in addressing needs and gaps through Big Data technology, How Payers de-risk their reimbursement and coverage decisions with early stage startups, the role of Big Data in informing the movement toward value-based healthcare, Enterprise focus areas across 7 major applications: Diagnostic, Preventative, Precision Medicine, Adverse medication events, Cost reduction, Medical research Population health, etc. Highmark's VITAL has projects in the top 5 areas, these area are not mutually exclusive.
Value Based Care Model
Inadequate Evidence
Solution
Traversing “Valley of Death”
De-risking Reimbursement
Vital Innovation
Conclusion
Focus areas for evidence development
The Attune LIS is a leading Cloud based lab information system that integrates all departments and centers spread across locations on a stable and secure platform, giving decision makers a unified picture of their business. Attune LIS improves accuracy while accelerating TAT and helping scale business rapidly.
The latest in advanced technology and digital capabilities are changing the way the life sciences industry develops new, life-changing treatments for patients.
Strokepad is a comprehensive, real-time, point-of-care digital clinical record specifically designed for stroke patients, encompassing the entire management pathway from admission to discharge.
It is a highly optimized, digital tablet interface with 'pen and paper' functionality, eliminating the need for dual entry or the use of parallel paper records throughout the care pathway.
Strokepad contains a built-in data field management which optimizes the collection of clinical and managerial data, reducing revenue loss through inaccurate coding.
Strokepad fully automates the processing of outcome data which eliminates resource intensive duplicate data collection for reporting and audit.ion of clinical and managerial data, reducing revenue loss through inaccurate coding.
The fundamental source of cost and error is in duplication:
^The clinician or nurse inputs the patients data directly into StrokePad at the bedside
^No duplication
^No data misunderstandings
^No duplicate recordings
^Reduced costs
^Reduced errors
More time for patient care
mHealth Israel_Ben Echeazu_Highmark Health_ Startups Engaging with US PayersLevi Shapiro
Presentation by Ben Echeaz, Business Development Director, Highmark Health, March 25, 2019, for the mHealth Israel community: Startups Engaging with US Payers. Includes overview of the US Payerand health insurance sector, Relationship to Blue Cross Blue Shield, Challenges in addressing needs and gaps through Big Data technology, How Payers de-risk their reimbursement and coverage decisions with early stage startups, the role of Big Data in informing the movement toward value-based healthcare, Enterprise focus areas across 7 major applications: Diagnostic, Preventative, Precision Medicine, Adverse medication events, Cost reduction, Medical research Population health, etc. Highmark's VITAL has projects in the top 5 areas, these area are not mutually exclusive.
Value Based Care Model
Inadequate Evidence
Solution
Traversing “Valley of Death”
De-risking Reimbursement
Vital Innovation
Conclusion
Focus areas for evidence development
The Attune LIS is a leading Cloud based lab information system that integrates all departments and centers spread across locations on a stable and secure platform, giving decision makers a unified picture of their business. Attune LIS improves accuracy while accelerating TAT and helping scale business rapidly.
The latest in advanced technology and digital capabilities are changing the way the life sciences industry develops new, life-changing treatments for patients.
Leverage near real-time data with risk-based, adaptive site monitoring to identify issues and trigger targeted actions that proactively mitigate threats to a clinical trial's success.
Our INTIENT Clinical suite of tools provides simplified collection, cleansing and management of clinical data, as well as faster, improved access through smart analytics and intelligent data flow. Visit https://accntu.re/2Eaov8N to learn more.
We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry.
Instrument of Change: Creating the next generation of Laboratory MiddlewareTodd Winey
These healthcare challenges create opportunities for the next generation of middleware to provide even more value to labs and the clinicians who depend on them. It requires a shift in thinking about the place and role of lab middleware, as it evolves from an operational tool to a platform that serves all of the business needs associated with running a laboratory.
With deep industry knowledge, OneSource addresses your lab requirements to help optimize your business outcomes, delivering everything from
everyday instrument repair to data integrity services. OneSource takes a one-of-kind managed approach, utilizing a powerful, interwoven suite of
solutions including analytics, compliance, laboratory computing, scientific lab support, asset management, lab relocation, and other services.
Using JReview to Analyze Clinical and Pharmacovigilance Data in Disparate Sys...Perficient, Inc.
Sponsors and CROs naturally rely on various clinical and safety systems from a multitude of software vendors. However, continuously accessing disparate sources for the reporting, analysis, and monitoring of data can be a treacherous undertaking, if you don't have a solution that connects to them right out of the box.
That's where JReview comes in. For almost two decades, life sciences companies, research organizations, in addition to the government, have relied on JReview for the comprehensive analysis and monitoring of clinical and pharmacovigilance data.
The analytics solution works with many Oracle Health Sciences applications, including Argus Safety, Oracle AERS, Oracle Clinical (OC), Remote Data Capture (RDC), Thesaurus Management System (TMS), InForm, Life Sciences Data Hub (LSH), and Clinical Development Center (CDC). JReview also works with non-Oracle solutions, such as ARISg, Medidata Rave, and SAS Drug Development.
In this slideshare, you will learn:
The features and benefits of JReview, including the new functionality in v10.0 (e.g., risk-based monitoring analytics reporting on the clinical data itself, etc.)
Benefits of using JReview for:
Reporting and query of your clinical data
Supplying internal and/or external users/sponsors information
Providing a secure way for your internal users and/or sponsor users to access the clinical data
Examples of how customers use JReview with OC/RDC
The implementation process and options
White paper explores Intel’s latest SSD technology, new Carestream solutions, the impact for PACS, and a look at the future of medical imaging data, access, storage and analysis.
DataArt is a global software engineering firm that takes a uniquely human approach to solving problems. With over 20 years of experience, teams of highly-trained engineers around the world, deep industry sector knowledge, and ongoing technology research, we help clients create custom software that improves their operations and opens new markets. Powered by our People First principle, we work with clients at any scale and on any platform, and adapt alongside them as they evolve.
Similar to Xcellerate Brochure - Successful Clinical Trials Begin and End with the Right Data. (20)
Genomics Solutions - Single Target to Whole Genome AnalysisCovance
With applied Genomics expertise, global co-location with Central Labs and solutions from biomarker discovery to CDx, our genomics solutions will help make your Precision Medicine drug development a reality.
Medical Device and Diagnostics Solutions for Every Stage of Your Product's De...Covance
Getting a medical device to the patient takes more than good technology in today's environment. Compelling evidence and convincing value proposition matter. Competing priorities and differing stakeholder definitions of value are driving the need for creative, connected strategies to get the most from each step in the development process. And - as evidence is gathered - it should be used to inform and iterate regulatory, reimbursement and clinical post-market strategies.
Pharmacovigilance Risk Management for BiosimilarsCovance
This paper focuses on pharmacovigilance (PV) and risk management for biosimilars, the issues and challenges faced in monitoring their safety and possible solutions.
Cell & Gene Therapy post-approval solutions to reduce scientific, regulatory and commercial risks, and accelerate development wherever you are in your product's development.
Cell & Gene Therapy enterprise development solutions to reduce scientific, regulatory and commercial risks, and accelerate development wherever you are in your product's development.
Cell & Gene Therapy Clinical Development SolutionsCovance
Cell & Gene Therapy clinical development solutions to reduce scientific, regulatory and commercial risks, and accelerate development wherever you are in your product's development.
Inhalation Technology - The Future of Effective Respiratory TreatmentsCovance
Nonclinical development channels: technical strategies, formulations and devices. Conventionally, inhaled drugs have been used to deliver medicines targeted at the most widespread respiratory diseases - specifically, chronic obstructive pulmonary disease (COPD) and asthma.
The Challenges Associated with Evaluating the Cost Benefit of Gene Therapies ...Covance
Despite the growing availability of approved gene therapies, decision-makers face significant challenges when evaluating pricing and reimbursement of these novel therapeutics. From determining cost-benefit ratios, setting out patient access criteria and designing reimbursement plans, this white paper explores some of the complex aspects of value assessment for gene therapies, and discusses results from a survey of key decision-makers across Germany, Sweden and the UK responsible for making pricing and reimbursement decisions.
Environmental Risk Assessment for Pharmaceutical DrugsCovance
Understanding the Evaluation and Implications of Findings to the Regulatory Review of Human Medicines in the Environment. Pharmaceutical drugs are intended for the treatment of human disease, therefore the risk of their environmental exposure in clinical use needs to be evaluated. Environmental risk assessment (ERA) is part of the requirements when applying for marketing approval in many geographic regions throughout the world.
Getting Investigators Onboard: Lab Preferences Make a Difference in Trial Par...Covance
Clinical trials are becoming increasingly complex and competitive, so attracting the best investigator sites to participate in a trial is a crucial step in meeting patient enrollment targets. Learn more about how investigator preference can help meet trial recruitment milestones.
Putting the Patient First: Launching a Comprehensive Patient-Centric ProgramCovance
Following a successful sponsor/CRO partnership in which Covance supported a large sponsor's reimbursement call center, a solid partnership had formed, founded on trust and a shared culture. The sponsor expanded this partnership with Covance with the desire to seamlessly transition another reimbursement support program from their current vendor. With the additional successful execution of this project, the sponsor selected Covance as their partner to consolidate all existing hub programs, build a tailored customer relationship management (CRM) tool and develop programs focused on the sponsor's specific needs and enhanced new therapeutic areas and markets.
Top 15 Pharma Gains an Edge in a Highly Competitive Specialty MarketCovance
Due to the complex nature of patient access and reimbursement process for specialty products, the client required a customized hub program to support multiple products, across several therapeutic areas. The unique intricacies of the initiative required a trusted strategic partner who could help advise, inform and support an innovative patient-centric program. In addition to possessing the right expertise and processes, the vendor needed to have a flexible technology platform that could be tailored to support the multiple brand requirements and deliver a seamless experience to various stakeholders including patients, healthcare professionals (HCPs) and specialty pharmacies.
Field Services: Providing On-Site, Field-Based Assistance to Support Customer...Covance
Ensuring access for patients can be complex and impacted by ever-changing factors that require an adaptable and responsive holistic solution to help provider and patients. Relying on a consultative approach, policy expertise and decades of experience, Covance Market Access deploys a variety of different filed-based teams that are tailored to meet your objectives and simplify access for your product.
Overcome the unique challenges of late-phase product development and generate the right data to support your products' objective. Products in late-phase development have complex needs and demands. Programs at this phase support new indications, value communication, adherence strategies, safety and efficacy and more.
Optimizing Each Patient's Product Access ExperienceCovance
Relying on a consultative approach, deep expertise and decades of experience, we work collaboratively with clients to deliver a successful product launch, program transition or program enhancement. Clients benefit from our market insights, strategic and unique approach and ability to continuously refine our processes.
Covance, in partnership with Oracle, offers a full-service, validated, private cloud, single-tenancy solution based on Argus technology, which enables faster and better safety decisions. This automated and integrated solution allows for easy scientific querying and analytics, which improves the quality and efficiency of safety operations. It also enhances compliance with E2B exchange for expedited and periodic reporting, allowing the organization to conduct global case processing, which can scale to tens of thousands of annual cases.
Plant Metabolism Studies: Options for Plant CultivationCovance
Regulators across the world are concerned with ensuring that any residues left in or on a crop after application of a plant protection product (PPP), present minimal risk to the health of humans and animals. To achieve this, regulators need information on the identity of the residues and the levels of residues remaining in or on a crop, in order to assess dietary risk and set maximum residue levels (MRLs). The testing approaches used are harmonized across most countries worldwide, focusing on the Organization for Economic Co-operation and Development (OECD) Test Guidelines (TGs) for pesticide residue chemistry. This e-book paper focuses on the laboratory-based plant cultivation methods that underlie the success of OECD crop metabolism studies, namely TG 501 and 502.
Business Solutions with .NET Development in Quantum Computing.pdfQServices Inc.
Unlock the power of quantum computing with QServices. Our .NET experts deliver cutting-edge solutions to drive your business forward. Experience the future of computing and gain a competitive edge today.
Colors of Wall Paint and Their Mentally Properties.pptxBrendon Jonathan
Discover how different wall paint colors can influence your mood and mental well-being. Learn the psychological effects of colors and find the perfect hue for every room in your home.
Comprehensive Water Damage Restoration Serviceskleenupdisaster
Find out how Disaster Kleenup's professional water damage restoration services can quickly and efficiently restore your property. Find more about our advanced techniques and quick action plans. Visit here: https://iddk.com/disaster-cleanup-services/flood-damage/
A Bulgarian work permit is valid for up to one year, after which it can be renewed as long as the conditions of employment have not changed. After obtaining a work permit, the employee will need to apply for a Type D visa at the Bulgarian embassy or consulate in their country. Urgent requirement for Bulgaria 🇧🇬🇧🇬work D Category National Permit Visa ( Indian /Nepali Nationality only) Visa Validity - 3 to 6 months on renewables basis. Job category - General worker/ Helper Salary - 800 Euro @ 8 hrs.+ Over time extra Age- 20- 40 years Total processing time -4-5 Months
Upvc Bathroom Doors Price and Designs In Keralabpshafeeque
UPVC Bathroom Doors Price in Kerala
When renovating or designing a bathroom, the choice of doors plays a pivotal role in ensuring both functionality and aesthetics. In Kerala, UPVC (Unplasticized Polyvinyl Chloride) bathroom doors have gained popularity for their durability, water resistance, and modern designs. This article delves into the pricing of UPVC bathroom doors in Kerala and why they are a preferred choice for homeowners.
#### Benefits of UPVC Bathroom Doors
UPVC bathroom doors offer several advantages, making them an ideal choice for the humid climate of Kerala:
1. **Water Resistance**: Unlike wooden doors, UPVC doors do not swell or warp when exposed to moisture, making them perfect for bathrooms.
2. **Durability**: These doors are resistant to termites and corrosion, ensuring a long lifespan.
3. **Low Maintenance**: UPVC doors require minimal upkeep, saving homeowners time and effort.
4. **Energy Efficiency**: They provide good insulation, helping maintain a comfortable bathroom temperature and reducing energy costs.
5. **Aesthetic Variety**: Available in various colors and designs, UPVC doors can complement any bathroom decor, from modern to traditional.
#### Price Range of UPVC Bathroom Doors in Kerala
The cost of UPVC bathroom doors in Kerala varies depending on factors such as size, design, and additional features. Here's a general overview of the price range:
- **Basic Models**: Simple UPVC bathroom doors start from ₹2,500 to ₹5,000. These doors are functional and offer essential benefits like water resistance and durability.
- **Mid-Range Models**: For more intricate designs or additional features such as frosted glass panels or metallic handles, prices range between ₹5,000 and ₹10,000.
- **Premium Models**: High-end UPVC bathroom doors, which may include custom designs, advanced locking systems, and superior finishes, can cost anywhere from ₹10,000 to ₹20,000 or more.
#### Conclusion
UPVC bathroom doors are an excellent investment for homes in Kerala, offering a blend of practicality and style. With a wide range of prices and designs available, homeowners can easily find a UPVC door that fits their budget and enhances their bathroom’s aesthetic appeal. When choosing a UPVC bathroom door, consider the specific needs of your space and the long-term benefits these doors provide. Investing in a quality UPVC bathroom door ensures a durable, low-maintenance, and stylish addition to your home.
Delightful Finds: Unveiling the Power of Gifts Under 100JoyTree Global
Stretch your budget and spread joy! This guide explores the world of gifts under 100, proving thoughtful gestures don't require a hefty price tag. Discover unique and practical options for birthdays, holidays, or simply showing someone you care. Find inspiration for every occasion within your budget!
Unlock the potential of Ruby on Rails for your next project. Hire RoR Developers from Semiosis for scalable and efficient web solutions. With expertise in RoR development, our team crafts robust applications to meet your business goals. Dial +1 9177322215 to collaborate with us and elevate your online presence.
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Courier & Package Tracking System Actually WorksIn Targos
In the world of modern logistics, the courier and package tracking system stands as a pivotal tool, offering transparency and efficiency throughout the shipping process. Let’s delve into the intricacies of courier and package tracking systems and explore how INTARGOS plays a key role in this domain.
The Jamstack Revolution: Building Dynamic Websites with Static Site Generator...Softradix Technologies
In this infographic, the Jamstack architecture emphasizes pre-rendered content and decoupling the frontend from the backend. It leverages static site generators (SSGs) to create fast-loading HTML files and APIs for dynamic functionality. Benefits include improved performance, enhanced security, scalability, and ease of deployment. Real-world examples include Netlify, Gatsby, and Contentful. https://softradix.com/web-development/
What Are the Latest Trends in Endpoint Security for 2024?VRS Technologies
In this PDF, Discover the top 2024 endpoint security trends, including zero trust, AI integration, XDR, cloud security, and enhanced mobile protection. VRS Technologies LLC supplies the top level Endpoint Security Service Dubai. For More Info Contact us: +971 56 7029840 Visit us: https://www.vrstech.com/endpoint-security-solutions.html
Learn about Inspect Edge, the leading platform for efficient inspections, featuring the advanced NSPIRE Inspection Application for seamless property assessments. Discover how the NSPIRE Inspection Application by Inspect Edge revolutionizes property inspections with advanced features and seamless integration.
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Xcellerate Brochure - Successful Clinical Trials Begin and End with the Right Data.
1. Graphically height-
ed claim: 48/50 of
the best selling
drugs of 2013 were
developed with
Covance Central
Successful clinical trials begin
and end with the RIGHT data.
As clinical trials become more complex and data-driven, you need to have
unprecedented access to all your clinical trial data to make more timely,
informed decisions and enable complete clinical trial optimization. At
Covance, we understand. We’ve been in the clinical trial business for
over 20 years and we know how important it is for you to have the right
data to help you bring drugs to market with speed, but more
importantly, drugs that are safe for patients.
Uncover new possibilities for your
clinical trials with Xcellerate®
, a fully
integrated informatics platform.
2. The clinical trial of
the FUTURE.
ONE comprehensive platform.
UNPARALLELED RESULTS.
Are you ready? The clinical trial of the future will be highly
predictive – with built-in capabilities that detect risks and protocol
deviations before they hinder progress. For this reason, Covance
has developed the most advanced clinical trial management
software available – the Xcellerate Informatics Suite. The
Xcellerate Informatics Suite was built from the ground up as a
single, unified platform to advance the entire clinical trial process
and reduce delays. Powerful analytics help extract information
from data that enable you to make smarter decisions. With a unique
combination of advanced data integration, clinical informatics and
operational expertise, this award-winning* suite reduces the cost,
time and complexity associated with clinical trials.
*2016 Fierce Innovation Award Winner: Life Sciences Edition in the Data Analytics/Business Intelligence
2018 SCRIP Award: Best Technological Development in Clinical Trials (Clinical Sponsor Focused) - Xcellerate CRA Dashboard
2019 Frost & Sullivan Global Contract Research Organization (CRO) Customer Value Leadership Award
3. BENEFITS OF XCELLERATE:
Xcellerate Trial Design
The Xcellerate Informatics Suite:
Covance has access to more clinical trial data than any other CRO, adding more than
500,000 medical sample results daily to our comprehensive historical database.
The Xcellerate Trial Design solution leverages our extensive knowledgebase to provide
insights into site selection, patient recruitment and resource allocation.
▶ Future-proof: custom-built architecture designed to scale to current and future data volumes
▶ Agnostic: integrates into existing trial management source systems
▶ Easy to use: user-centric web and mobile user interfaces
▶ Effective: fast access to critical information with visualizations for metrics reporting & trending
▶ Efficient: advanced workflow engine to accelerate and automate issue resolution
▶ Compliant: audit trail and history tracking supports adherence to ICH GCP and other guidelines
Components of Covance Informatics Suite
**Also Available as Software as a Service (SaaS)