This document summarizes the Cortellis Clinical Trials Intelligence product. It provides access to over 130,000 clinical trials from around the world across various therapeutic areas. Users can access the data through a web portal or integrate it with other systems using APIs. The platform offers powerful search and filtering capabilities along with dynamic visualizations to analyze trial findings and competitive intelligence. It aims to help users accelerate strategic clinical development decisions and advance personalized medicine.
What Happens After Your Device is Approved? Collecting Data in the Real WorldMedpace
In this workshop, Medpace will discuss key considerations for generating real-world evidence and how to apply critical insights in order to drive late-stage clinical research. To listen to this presentation, visit https://vimeo.com/168768256
Here is the slideset I presented at the 2nd International Conference on Business Analytic and Intelligence (ICBAI). The intent behind the paper/presentation was to bring out awareness on AE analysis and present status of AE data in india. Certainly there are huge potential benefit/insights out of this data if the base is set well. Private health care institutions can reap the benefit (Both financial and patient care) if they invest to define the system for their use.
From Edge Case to Main Case, Michelle Longmire of Medable_mHealth IsraelLevi Shapiro
Presentation by Michelle Longmire, CEO of Medable, April 20, 2021, for mHealth Israel. During CoVID, as physical access to clinics was limited, Medable enabled patients to continue participating in critical research efforts. Medable Supporting over 100 Studies Across a Diverse Array of Therapeutic Areas. Medable provides a platform for seamless evidence
generation, across the entire patient journey. Connecting patients globally for community, care, and research. Improve patient experience and retention. Reduce site burden. Data Cloud & Platform should be flexible and modular to enable protocol-fit digital. Medable Digitome, for data driven decentralized trials and a new era of understanding patients, therapies, and conditions. Clinical research is a small component of the broader healthcare journey. Enable health data and evidence generation from clinical to commercial, from day one. Continuous health data & evidence from clinical to commercial and beyond. The Digitome can provide a
primary observational protocol that collects large scale baseline data in a framework that enables streamlined recruitment, enrollment, and participation into interventional clinical substudies.
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.
Real-world Evidence A Saudi Regulatory PerspectiveUN SPHS
By Mr. Turki A. Al-Thunian, Bpharm, MClinPharm, MSc.Epi, PhD, Acting Director of the Research Informatics Department, Saudi Food and Drug Authority (SFDA), delivered at the Global Forum 2020 Drug Safety and Supply Chains session.
Automate your literature monitoring for more effective pharmacovigilanceAnn-Marie Roche
Embase and QUOSA experts take you through a complete literature management workflow, demonstrating how Elsevier’s Pharmacovigilance solution enables efficient and comprehensive post-market surveillance.
Customized Oncology Development Solutions: Clinical Trials Designed Around You®Covance
Oncology is one of the most research-intensive therapeutic areas, yet no two development programs are the same. No two trials are the same. Each one calls for a customized strategy and distinct trial management approach. Covance develops fit-for-purpose solutions Designed Around You® that enable more efficient clinical trials and focus on what is most valuable to your organization.
What Happens After Your Device is Approved? Collecting Data in the Real WorldMedpace
In this workshop, Medpace will discuss key considerations for generating real-world evidence and how to apply critical insights in order to drive late-stage clinical research. To listen to this presentation, visit https://vimeo.com/168768256
Here is the slideset I presented at the 2nd International Conference on Business Analytic and Intelligence (ICBAI). The intent behind the paper/presentation was to bring out awareness on AE analysis and present status of AE data in india. Certainly there are huge potential benefit/insights out of this data if the base is set well. Private health care institutions can reap the benefit (Both financial and patient care) if they invest to define the system for their use.
From Edge Case to Main Case, Michelle Longmire of Medable_mHealth IsraelLevi Shapiro
Presentation by Michelle Longmire, CEO of Medable, April 20, 2021, for mHealth Israel. During CoVID, as physical access to clinics was limited, Medable enabled patients to continue participating in critical research efforts. Medable Supporting over 100 Studies Across a Diverse Array of Therapeutic Areas. Medable provides a platform for seamless evidence
generation, across the entire patient journey. Connecting patients globally for community, care, and research. Improve patient experience and retention. Reduce site burden. Data Cloud & Platform should be flexible and modular to enable protocol-fit digital. Medable Digitome, for data driven decentralized trials and a new era of understanding patients, therapies, and conditions. Clinical research is a small component of the broader healthcare journey. Enable health data and evidence generation from clinical to commercial, from day one. Continuous health data & evidence from clinical to commercial and beyond. The Digitome can provide a
primary observational protocol that collects large scale baseline data in a framework that enables streamlined recruitment, enrollment, and participation into interventional clinical substudies.
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.
Real-world Evidence A Saudi Regulatory PerspectiveUN SPHS
By Mr. Turki A. Al-Thunian, Bpharm, MClinPharm, MSc.Epi, PhD, Acting Director of the Research Informatics Department, Saudi Food and Drug Authority (SFDA), delivered at the Global Forum 2020 Drug Safety and Supply Chains session.
Automate your literature monitoring for more effective pharmacovigilanceAnn-Marie Roche
Embase and QUOSA experts take you through a complete literature management workflow, demonstrating how Elsevier’s Pharmacovigilance solution enables efficient and comprehensive post-market surveillance.
Customized Oncology Development Solutions: Clinical Trials Designed Around You®Covance
Oncology is one of the most research-intensive therapeutic areas, yet no two development programs are the same. No two trials are the same. Each one calls for a customized strategy and distinct trial management approach. Covance develops fit-for-purpose solutions Designed Around You® that enable more efficient clinical trials and focus on what is most valuable to your organization.
Andwin Scientific specializes in Clinical Supplies and Equipment product manufacturing, sourcing, procurement, storage and distribution as a supplier to global life science organizations and a distributor to direct end using companies (including sites). This makes Andwin Scientific the only company that offers true consolidation for clinical studies by facilitating the purchase of products from various suppliers in one transaction.
This presentation summarizes our research on 40 companies from around the world that are leveraging Artificial Intelligence to improve the Healthcare Industry. They are all well-funded, have highly qualified CEOs & Boards, and are poised to achieve their product development milestones.
The I-Square Ventures proprietary rating algorithm indicates that almost all of these companies will receive more funding, and/or be acquired by larger companies.
Service Overview
Site management services to CRO and SITE:
A) Pre initiation
Identification of Potential Sites
Faster Feasibility
Site set up, supplies and other infrastructure needs
Regulatory and IEC/ IRB communications
Rapid negotiation of CTA
Setting up Standard Operating Procedures (SOPs)
B) During Study Duration
Provide dedicated trained and experienced CRCs (Clinical research coordinators)
Patient recruitment & retention Support
Maintenance of essential documents
Source documentation as per ALCOA standards (Attributable, Legible, Contemporaneous, Original & Accurate
Regular IP (Investigational Product) accountability and storage
Completion of CRF’s within timelines
Faster query resolution
Reporting of AE, SAEs within timelines
Support Monitoring visits and Quality Assurance audit action items.
Patient visit Follow Up and compliance assistance
Preparation of site for monitoring and audits/ inspections
C) Post Close out
· Archiving of site results and documents
Site Identification
Faster Feasibility
Ready Sites
How BrackenData Leverages Data on Over 250,000 Clinical TrialsBracken
Learn about our why we've created our clinical trial intelligence solutions, how they provide big value to teams in the life sciences industry, and how you can start leveraging data immediately.
The Hub – Solutions Distinctly for Nimble Biotechs Brochure Covance
Welcome to a unique experience - one that's Designed Around You®. Where you control your journey from start to finish. Regardless of where you are and how far you aspire to go, choose the options that make the most of your endeavor. Learn more about the innovations you can tap at any stage of the drug development process.
Access the webinar: http://goo.gl/p08pTz
These slides were presented in a webinar by Denodo in collaboration with BioStorage Technologies and Indiana Clinical and Translational Sciences Institute and Regenstrief Institute.
BioStorage Technologies, Inc., Indiana Clinical and Translational Sciences Institute, and Regenstrief Institute (CTSI) have joined Denodo to talk about the important role of technological advancements, such as data virtualization, in advancing biospecimen research.
By watching this webinar, you can gain insight into best practices around the integration of biospecimen and research data as well as technology solutions that provide consolidated views and rapid conversions of this data into valuable business insights. You will also learn how data virtualization can assist with the integration of data residing in heterogeneous repositories and can securely deliver aggregated data in real-time.
Clinical Biometrics, Inc. Executive Overview
Description Clinical Biometrics is an organization dedicated to enabling predictive healthcare and disease prevention with the IoT. We are working on the IoT (Internet of Things) wireless, biomedical patient monitoring and vendor agnostic integration, pioneering programmable biosensors, integration products and services to monitor secure clinical data in real-time and over time, for inpatient and outpatient environments. Our model enables predictive and preventative healthcare delivery. We are developing vendor agnostic middleware that will allow the integration of the various vendor's sensors and protocols into a common platform with rich data analytics capabilities. This technology will impact our healthcare paradigms and usher us into the future of healthcare delivery including real-time predictive healthcare and disease prevention.
- Tim Crammer, CEO
This program, targeted to small and medium sized biotech firms globally, allowed hundreds of companies to experience the new platform and generated significant new revenue for the organization.
The QualityNet Hospital-Specific Report, Readmissions Penalties, & Your HospitalMichael Passanante
The CMS Hospital Readmissions Reduction Program (HRRP) was effective for Medicare discharges beginning on October 1, 2012 and reduces payments to IPPS hospitals with excess readmissions. In FY 2015, over 2,600 hospitals will receive lower Medicare payments totaling $428 million in penalties. This is an increase of over $200 million from FY 2014. It is essentially impossible for hospitals to calculate their own readmission penalty.
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RMD24 | Debunking the non-endemic revenue myth Marvin Vacquier Droop | First ...BBPMedia1
Marvin neemt je in deze presentatie mee in de voordelen van non-endemic advertising op retail media netwerken. Hij brengt ook de uitdagingen in beeld die de markt op dit moment heeft op het gebied van retail media voor niet-leveranciers.
Retail media wordt gezien als het nieuwe advertising-medium en ook mediabureaus richten massaal retail media-afdelingen op. Merken die niet in de betreffende winkel liggen staan ook nog niet in de rij om op de retail media netwerken te adverteren. Marvin belicht de uitdagingen die er zijn om echt aansluiting te vinden op die markt van non-endemic advertising.
What are the main advantages of using HR recruiter services.pdfHumanResourceDimensi1
HR recruiter services offer top talents to companies according to their specific needs. They handle all recruitment tasks from job posting to onboarding and help companies concentrate on their business growth. With their expertise and years of experience, they streamline the hiring process and save time and resources for the company.
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A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
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Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
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Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
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Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
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Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
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CTI Landing Page
1. Cortellis Clinical Trials Intelligence
LIFe SCIeNCeS SoLUTIoNS
CLEARLY CORTELLIS
Cover over 130,000 U.S.
and global clinical trials
for biomarkers, devices,
biologics and drugs.
Integrated with extensive
scientific and competitive
intelligence.
The complete
picture
Precision medicine
strategies
Clear insights
at a glance
Fast discoveries—
anywhere
Access our clinical content
from the iPad compatible
Cortellis web portal.
Or easily integrate your
proprietary content with our
API solutions.
Save time analyzing your
findings with clear and
dynamic visualizations.
Enhancing your fact-based
decision making and
competitive positioning.
Get the right information
for your clinical strategy—
including rare diseases.
With powerful searching,
filtering and exporting, for
both novices and experts.
Accelerate your strategic clinical development
decisions — and advance patient care and
personalized medicine. Coming soon.
Benefits & Features +
Related Articles +
let us know
Care to learn more?
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Care to learn more?
2. Benefits & Features
Access all clinical, competitve and scientific content from the iPad compatible
•
Cortellis web portal.
Integrate content into other applications and platforms in real-time through a
•
suite of APIs (Application Programming Interface).
Incorporate your proprietary content and custom annotations through our
•
Integration Solutions.
—
Related Articles
CLINICAL TRIALS article
Assessing Drug Safety in Clinical Trials
Leveraging analytics to answer common questions about
drug safety across classes of drugs or competing drug
candidates.
Download the article
pharma matters report
Developments in Clinical Trials - coming soon
Correlating biomarker discovery with clinical trial evidence
for the fight against existing, common ailments.
Book your free copy
—
Trusted Global Intelligence
Best-in-Class Technology
Dynamic Analytic Tools
Over 130,000 US and global trials from more than 20,000 sources.
•
More than 200,000 press releases indexed to clinical trial types or events.
•
2.5 million articles related to clinical outcomes or development since the
•
1960s.
Over 21,000 meeting abstracts and 8,000 conference reports.
•
Powerful indexing with enhanced searching and filtering options to retrieve and
•
analyze information by drug class, technology, disease therapy, and more.
Granular quantified outcomes to assess competitive landscape, patient
•
response and CER.
Robust exporting capability (up to 5,000 records at once).
•
Customizable views and alerting options.
•
View distribution of indication, intervention, sponsor, phase, recruitment status,
•
country design, and active control.
Fast insight into trial timelines and disease segmentation with dynamic
•
visualizations.
Save visualizations in PowerPoint so findings can be easily updated and
•
shared with key stakeholders.
Our team of experts can customize analytics and reporting to meet your unique
•
business challenges.
Flexible Access & Integration
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