Presentation by Dr Merran Smith, PHRN, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Adrian Burton, ARDC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Prof Lisa Askie, ANZCTR, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Davina Ghersi, NHMRC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
International perspective for sharing publicly funded medical research dataARDC
Presentation by Olivier Salvado, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Kelly Hart, ONDC in PM&C, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Adrian Burton, ARDC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Prof Lisa Askie, ANZCTR, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Dr Davina Ghersi, NHMRC, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
International perspective for sharing publicly funded medical research dataARDC
Presentation by Olivier Salvado, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Kelly Hart, ONDC in PM&C, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Strengthening data sharing for public health: ethical, legal and political is...ExternalEvents
http://www.fao.org/about/meetings/wgs-on-food-safety-management/en/
Strengthening data sharing for public health: ethical, legal and political issues. Presentation from the Technical Meeting on the impact of Whole Genome Sequencing (WGS) on food safety management and GMI-9, 23-25 May 2016, Rome, Italy.
Samantha Robertson - NHMRC Perspectives on Increasing Access to Data from Pub...Wiley
Governments and industries all over the world are tackling the challenges and opportunities of ‘Big Data’. In view of these challenges, the key drivers of change in this area are the behaviour of researchers, the introduction of incentives or rewards and funding for data sharing infrastructure. Governments and taxpayers also expect a return on investment from the money spent on publically funded research. Building on and learning from the successes (and failures) of others need to be part of the research vernacular. Issues such as open access, data curation, handling of data, and sharing of that data are all matters on which the National Health and Medical Research Council (NHMRC) has an interest in. NHMRC works with the sector to develop best practise policies on such matters.
Samantha Robertson
Executive Director, NHMRC Evidence, Advice & Governance
Presented at the 2015 Wiley Publishing Seminar, 5 November, Melbourne, Australia.
Sharing and standards christopher hart - clinical innovation and partnering...Christopher Hart
Acknowledging the increasing need for cooperation and collaboration in data sharing and access. Describing the complexity that this can bring. Then describing some of the ways to simplify that.
Originally presented at Terrapin's Clinical innovation and partnering world March 8-9 2017.
http://www.terrapinn.com/conference/innovation-and-partnering/index.stm
GlobalSurg global surgery research collaboration - GASOC presentation in OxfordDr Edward Fitzgerald
GlobalSurg was established to represent practising surgeons from around the world and support collaborative international research into surgical outcomes by fostering local, national and international research networks.
Our growing network now includes over 5000 clinicians in more than 100 countries. The ethos is inclusive and collaborative: our international cohort studies are open to all collaborators, including medical students, clinical officers, doctors, nurses and researchers.
We run annual research prioritisation events, allowing surgeons from all over world to contribute to the direction of the group.
Our cohort studies aim to give grass-root surgeons the opportunity to participate in major projects. They are designed to ensure easy delivery by local surgeons and will not require extra resources or funding. Every researcher who contributes data into a cohort study is a Pubmed-citable collaborator on study papers which will be published under one main name – GlobalSurg – to represent our group effort.
Informatics and Clinical Decision Support in Precision MedicineAndre Dekker
Talk given during http://www.miccai2015.org/ in Munich Germany. Part of the Satellite Workshop and Challenges in Imaging & Digital Pathology (https://wiki.cancerimagingarchive.net/x/JgM7AQ).
Work Package (WP) 12 – PEARL Barriers In search for an inventory and assessme...ExternalEvents
http://www.fao.org/about/meetings/wgs-on-food-safety-management/en/
International challenges regarding the future sharing of sequence data. Presentation from the Technical Meeting on the impact of Whole Genome Sequencing (WGS) on food safety management and GMI-9, 23-25 May 2016, Rome, Italy.
Ethical, Legal, and Social Implications of ELSI Learning Health Systems 2017 Conference, University of Michigan. Learning from the experience and outcomes of every cancer patient
Data management planning in the Australian funding landscape by Sarah OlesenMarta Ribeiro
Data management planning in the Australian funding landscape by Sarah Olesen at eResearch Australasia Conference
1.Australian Code for the Responsible Conduct of Research (2007)
2. National Statement on Ethical Conductin Human Research (2007 – updated 2014)
Leading by Success Impact of a Clinical & Translational Res.docxcroysierkathey
Leading by Success: Impact of a Clinical & Translational
Research Infrastructure Program to Address Health Inequities
Bruce Shiramizu1, Vicki Shambaugh2, Helen Petrovich2, Todd B. Seto3, Tammy Ho4,
Noreen Mokuau5, and Jerris R. Hedges4
1Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School
of Medicine (JABSOM), University of Hawaii at Manoa (UHM), Honolulu, HI
2Pacific Health Research and Education Institute, Honolulu, HI
3Department of Medicine, JABSOM, UHM, Honolulu, HI
4JABSOM, UHM, Honolulu, HI
5Myron B. Thompson School of Social Work, UHM, Honolulu, HI
Abstract
Building research infrastructure capacity to address clinical and translational gaps has been a focus
of funding agencies and foundations. Clinical and Translational Sciences Awards, Research
Centers in Minority Institutions Infrastructure for Clinical and Translational Research (RCTR) and
the Institutional Development Award Infrastructure for Clinical and Translational Research funded
by United States (US) government to fund clinical translational research programs have existed for
over a decade to address racial and ethnic health disparities across the US. While the impact on the
nation’s health can’t be made in a short period, assessment of a program’s impact could be a
litmus test to gauge its effectiveness at the institution and communities. We report the success of a
Pilot Project Program in the University of Hawaii RCTR Award in advancing careers of emerging
investigators and community collaborators. Our findings demonstrated that the investment has a
far-reaching impact on engagement with community-based research collaborators, career
advancement of health disparities investigators, and favorable impacts on health policy.
Keywords
health disparity; clinical research; health inequity; translational research
INTRODUCTION
Health inequities continue to persist in communities across the disease spectrum throughout
the United States (US) and globally1–3. Contributing to the culture of health disparities has
Correspondence: Bruce Shiramizu, 651 Ilalo Street, BSB 325AA, Honolulu, Hawaii, 96813; [email protected]
COMPLIANCE WITH ETHICAL STANDARDS
The scope of the work did not involve human participants as reviewed by the University of Hawaii Institutional Review Board.
The authors have no other potential conflicts of interests except for the funding agencies as acknowledged.
HHS Public Access
Author manuscript
J Racial Ethn Health Disparities. Author manuscript; available in PMC 2018 April 28.Au
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partly been a function of the imbalance of biomedical research funding from government
agencies, private foundations, industry and other sources4–7. Innovative concepts and bold
initiatives to increase collaborations and partnerships were established through government,
industry and fou ...
Strengthening data sharing for public health: ethical, legal and political is...ExternalEvents
http://www.fao.org/about/meetings/wgs-on-food-safety-management/en/
Strengthening data sharing for public health: ethical, legal and political issues. Presentation from the Technical Meeting on the impact of Whole Genome Sequencing (WGS) on food safety management and GMI-9, 23-25 May 2016, Rome, Italy.
Samantha Robertson - NHMRC Perspectives on Increasing Access to Data from Pub...Wiley
Governments and industries all over the world are tackling the challenges and opportunities of ‘Big Data’. In view of these challenges, the key drivers of change in this area are the behaviour of researchers, the introduction of incentives or rewards and funding for data sharing infrastructure. Governments and taxpayers also expect a return on investment from the money spent on publically funded research. Building on and learning from the successes (and failures) of others need to be part of the research vernacular. Issues such as open access, data curation, handling of data, and sharing of that data are all matters on which the National Health and Medical Research Council (NHMRC) has an interest in. NHMRC works with the sector to develop best practise policies on such matters.
Samantha Robertson
Executive Director, NHMRC Evidence, Advice & Governance
Presented at the 2015 Wiley Publishing Seminar, 5 November, Melbourne, Australia.
Sharing and standards christopher hart - clinical innovation and partnering...Christopher Hart
Acknowledging the increasing need for cooperation and collaboration in data sharing and access. Describing the complexity that this can bring. Then describing some of the ways to simplify that.
Originally presented at Terrapin's Clinical innovation and partnering world March 8-9 2017.
http://www.terrapinn.com/conference/innovation-and-partnering/index.stm
GlobalSurg global surgery research collaboration - GASOC presentation in OxfordDr Edward Fitzgerald
GlobalSurg was established to represent practising surgeons from around the world and support collaborative international research into surgical outcomes by fostering local, national and international research networks.
Our growing network now includes over 5000 clinicians in more than 100 countries. The ethos is inclusive and collaborative: our international cohort studies are open to all collaborators, including medical students, clinical officers, doctors, nurses and researchers.
We run annual research prioritisation events, allowing surgeons from all over world to contribute to the direction of the group.
Our cohort studies aim to give grass-root surgeons the opportunity to participate in major projects. They are designed to ensure easy delivery by local surgeons and will not require extra resources or funding. Every researcher who contributes data into a cohort study is a Pubmed-citable collaborator on study papers which will be published under one main name – GlobalSurg – to represent our group effort.
Informatics and Clinical Decision Support in Precision MedicineAndre Dekker
Talk given during http://www.miccai2015.org/ in Munich Germany. Part of the Satellite Workshop and Challenges in Imaging & Digital Pathology (https://wiki.cancerimagingarchive.net/x/JgM7AQ).
Work Package (WP) 12 – PEARL Barriers In search for an inventory and assessme...ExternalEvents
http://www.fao.org/about/meetings/wgs-on-food-safety-management/en/
International challenges regarding the future sharing of sequence data. Presentation from the Technical Meeting on the impact of Whole Genome Sequencing (WGS) on food safety management and GMI-9, 23-25 May 2016, Rome, Italy.
Ethical, Legal, and Social Implications of ELSI Learning Health Systems 2017 Conference, University of Michigan. Learning from the experience and outcomes of every cancer patient
Data management planning in the Australian funding landscape by Sarah OlesenMarta Ribeiro
Data management planning in the Australian funding landscape by Sarah Olesen at eResearch Australasia Conference
1.Australian Code for the Responsible Conduct of Research (2007)
2. National Statement on Ethical Conductin Human Research (2007 – updated 2014)
Leading by Success Impact of a Clinical & Translational Res.docxcroysierkathey
Leading by Success: Impact of a Clinical & Translational
Research Infrastructure Program to Address Health Inequities
Bruce Shiramizu1, Vicki Shambaugh2, Helen Petrovich2, Todd B. Seto3, Tammy Ho4,
Noreen Mokuau5, and Jerris R. Hedges4
1Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School
of Medicine (JABSOM), University of Hawaii at Manoa (UHM), Honolulu, HI
2Pacific Health Research and Education Institute, Honolulu, HI
3Department of Medicine, JABSOM, UHM, Honolulu, HI
4JABSOM, UHM, Honolulu, HI
5Myron B. Thompson School of Social Work, UHM, Honolulu, HI
Abstract
Building research infrastructure capacity to address clinical and translational gaps has been a focus
of funding agencies and foundations. Clinical and Translational Sciences Awards, Research
Centers in Minority Institutions Infrastructure for Clinical and Translational Research (RCTR) and
the Institutional Development Award Infrastructure for Clinical and Translational Research funded
by United States (US) government to fund clinical translational research programs have existed for
over a decade to address racial and ethnic health disparities across the US. While the impact on the
nation’s health can’t be made in a short period, assessment of a program’s impact could be a
litmus test to gauge its effectiveness at the institution and communities. We report the success of a
Pilot Project Program in the University of Hawaii RCTR Award in advancing careers of emerging
investigators and community collaborators. Our findings demonstrated that the investment has a
far-reaching impact on engagement with community-based research collaborators, career
advancement of health disparities investigators, and favorable impacts on health policy.
Keywords
health disparity; clinical research; health inequity; translational research
INTRODUCTION
Health inequities continue to persist in communities across the disease spectrum throughout
the United States (US) and globally1–3. Contributing to the culture of health disparities has
Correspondence: Bruce Shiramizu, 651 Ilalo Street, BSB 325AA, Honolulu, Hawaii, 96813; [email protected]
COMPLIANCE WITH ETHICAL STANDARDS
The scope of the work did not involve human participants as reviewed by the University of Hawaii Institutional Review Board.
The authors have no other potential conflicts of interests except for the funding agencies as acknowledged.
HHS Public Access
Author manuscript
J Racial Ethn Health Disparities. Author manuscript; available in PMC 2018 April 28.Au
th
o
r M
a
n
u
scrip
t
A
u
th
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a
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scrip
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a
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scrip
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A
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th
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scrip
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partly been a function of the imbalance of biomedical research funding from government
agencies, private foundations, industry and other sources4–7. Innovative concepts and bold
initiatives to increase collaborations and partnerships were established through government,
industry and fou ...
Growing the health and wealth of the nation through research, pop up uni, 11a...NHS England
Expo is the most significant annual health and social care event in the calendar, uniting more NHS and care leaders, commissioners, clinicians, voluntary sector partners, innovators and media than any other health and care event.
Expo 15 returned to Manchester and was hosted once again by NHS England. Around 5000 people a day from health and care, the voluntary sector, local government, and industry joined together at Manchester Central Convention Centre for two packed days of speakers, workshops, exhibitions and professional development.
This year, Expo was more relevant and engaging than ever before, happening within the first 100 days of the new Government, and almost 12 months after the publication of the NHS Five Year Forward View. It was also a great opportunity to check on and learn from the progress of Greater Manchester as the area prepares to take over a £6 billion devolved health and social care budget, pledging to integrate hospital, community, primary and social care and vastly improve health and well-being.
More information is available online: www.expo.nhs.uk
Professor Louisa Jorm - Director, Centre for Big Data Research in Health, UNSW Australia. http://www.garvan.org.au/news-events/leaders-in-science-and-society
The Philippine Council for Health Research and Development.docxJamaicaSalvador
The Philippine Council for Health Research and Development (PCHRD)
- is one of the three sectoral councils of the Department of Science and Technology (DOST).
- It is a forward-looking, partnership-based national body responsible for coordinating and monitoring research activities in the country.
- was created on March 17, 1982 through Executive order No. 784. In 1987, Executive Order No. 128 reaffirmed its existence and relevance. This directive reorganized the National Science and Technology Authority into what is now the Department of Science and Technology.
ABOUT PRACTICE-BASED RESEARCH NETWORKSSupporting Better Sc.docxransayo
ABOUT PRACTICE-BASED RESEARCH NETWORKS
Supporting Better Science in Primary Care: A
Description of Practice-based Research Networks
(PBRNs) in 2011
Kevin A. Peterson, MD, MPH, Paula Darby Lipman, PhD, Carol J. Lange, MPH,
Rachel A. Cohen, MPH, and Steve Durako, BA
Background: Bound by a shared commitment to improving medical care through systematic inquiry,
practice-based research networks (PBRNs) provide a basic laboratory for primary care research and
dissemination.
Methods: Data from US primary care PBRNs were collected as part of the 2011 Agency for Healthcare
Research and Quality PBRN registration process. Data addressed PBRN characteristics, research activi-
ties, and perceived strengths and weaknesses.
Results: One hundred forty-three primary care PBRNs were registered with the resource center in
2011, including 131 that were identified as either eligible for Agency for Healthcare Research and Qual-
ity recognition (n � 121) or as developing (n � 10). These PBRNs included 12,981 practices with more
than 63,000 individual members providing care to approximately 47.5 million people. PBRNs had an
average of 482 individual members (median, 170) from 101 practices (median, 32).
Conclusions: PBRNs are growing in experience and research capacity. With member practices serving
approximately 15% of the US population, PBRNs are adopting more advanced study designs, disseminat-
ing and implementing practice change, and participating in clinical trials. PBRNs provide valuable ca-
pacity for investigating questions of importance to clinical practice, disseminating results, and imple-
menting evidence-based strategies. PBRNs are well positioned to support the emerging public health
role of primary care providers and provide an essential component of a learning health care system.
( J Am Board Fam Med 2012;25:565–571.)
Keywords: Family Medicine Research, Practice-based Research, Practice-based Research Networks
Primary care practice-based research networks
(PBRNs) enhance the performance of clinical re-
search in community settings and speed the dissem-
ination of new knowledge into practice.1,2 Bound
by a shared commitment to improving medical care
through systematic inquiry, PBRNs provide a basic
laboratory for primary care research and dissemi-
nation involving every state and territory in the
United States.3,4 The ability of PBRNs to involve
“real-world” practices in clinical research provides
new opportunities to engage understudied popula-
tions, to study a range of health problems, and to
accelerate community adoption of new knowledge
and best practices.5,6
The Agency for Healthcare Research and Qual-
ity (AHRQ) has a long history of supporting pri-
mary care research networks. In 2002, the AHRQ
created the National PBRN Resource Center to
identify existing networks and promote growth in
their capacity for clinical research. Led initially by
the University of Indiana and National Opinion
Research Center at the University of Chicago, i.
The Clinical and Translational Science Awards (CTSA) Program: What can it do ...CTSciNet .org
Meeting: Physician-Scientist Career Development Meeting, New York Academy of Sciences, November 3-5, 2010
Panel: Successful Strategies for the Physician-Scientist
Presentation: The Clinical and Translational Science Awards (CTSA) Program: What can it do for you?
Speaker: Lisa Guay-Woodford, M.D., Professor and Vice Chair of Genetics, CTSA director, University of Alabama, Birmingham
View online with audio at http://community.sciencecareers.org/ctscinet/groups/sessions/2010/12/the-ctsa-program.php
IMPLEMENTING ELECTRONIC HEALTH RECORDS IN NEW ZEALAND: A CRITICAL APPRAISAL O...hiij
New Zealand health sector has increasing demands in theageing population and ongoing inflation of medical costs. These demands are growing, and the importance of technology could optimise the healthcare sector performance. Advancement in technology drives Electronic Health Records
implementation to add substantial value to health delivery systems. The investment and promotion of health informationinfrastructure have positioned New Zealand as a world leader in the field of primary care sector. Factors such as organisation structure, culture, leadership and workflow design are important to achieving successful implementation of Electronic Health Records. This review intends to critically appraise the advantages of EHRs over paper-based records (PBRs). It outlines the measures introduced by Ministry of Health to implement EHRs across the health sector in New Zealand. Furthermore, the review will provide an international comparison in implementing EHRs with that of New Zealand.
Contents:
- Facts & figures
- Ecosystem overview
- Unique assets: medical research, researchers and data
- Health tech & life sciences talent in the Helsinki region
- Success stories
- Universities and research
- Industry organisations
- Easy access to EU markets
- Finland - the most advanced testbed in the world
- Health tech & life sciences focus areas in the Helsinki region:
/ Med tech
/ Cancer treatment
/ Genomics & Precision medicine
/ Finngen
/ Digital health
Presentation by Dr Steve McEachern, ADA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Hugo Leroux and Liming Zhu, CSIRO, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Presentation by Prof Chris Rowe, ADNet, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
FAIR for the future: embracing all things dataARDC
FAIR for the future: embracing all things data - Natasha Simons, Keith Russell and Liz Stokes, presented at Taylor & Francis Scholarly Summits in Sydney 11 Feb 2019 and Melbourne 14 Feb 2019.
How to make your data count webinar, 26 Nov 2018ARDC
Slides from the 26 Nov Make your data count webinar. The research community has long grappled with the problem of assessing and tracking the results of scholarship. Research data is no exception. The Make Data Count (MDC) project (https://makedatacount.org/), funded by the Sloan Foundation, has delivered a data usage metric standard (Code of Practice) and a workflow for the retrieval and display of standardised usage and citation metrics in your repository interface.
Listen to this webinar to learn more about the Make Data Count project and the 5 steps you can take to make the data in your repository count. Hear from MDC project team members who have already implemented MDC in the dash (https://dash.ucop.edu) and DataOne (https://search.dataone.org/data) repositories. Learn from their experience, see the results.
Our international speaker line-up includes Daniella Lowenberg (California Digital Library) and Patricia Cruse (DataCite).
Recording available: https://youtu.be/Lkysz0Mc7fo
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
For more information, visit-www.vavaclasses.com
Safalta Digital marketing institute in Noida, provide complete applications that encompass a huge range of virtual advertising and marketing additives, which includes search engine optimization, virtual communication advertising, pay-per-click on marketing, content material advertising, internet analytics, and greater. These university courses are designed for students who possess a comprehensive understanding of virtual marketing strategies and attributes.Safalta Digital Marketing Institute in Noida is a first choice for young individuals or students who are looking to start their careers in the field of digital advertising. The institute gives specialized courses designed and certification.
for beginners, providing thorough training in areas such as SEO, digital communication marketing, and PPC training in Noida. After finishing the program, students receive the certifications recognised by top different universitie, setting a strong foundation for a successful career in digital marketing.
Azure Interview Questions and Answers PDF By ScholarHat
NCRIS and the health domain
1. NCRIS and the health domain
Merran Smith, Chief Executive, PHRN
ARDC Forum, Canberra, 6 March 2019
2. NCRIS overview
Australian Government’s National Collaborative Research
Infrastructure Strategy (NCRIS)
Managed by the Department of Education and Training,
with input from governments, universities and institutes
Supports a wide range of national research
infrastructure, including e-research/ARDC
3. NCRIS and health
Recent NCRIS documents (2016 Roadmap; Research Infrastructure Investment Plan)
highlight health in context of therapeutic development, through four capabilities:
Australian Phenomics Network (APN)
BioPlatforms Australia (BPA)
Therapeutic Innovation Australia (TIA)
Population Health Research Network (PHRN)
4. Focus of health capabilities
APN: Gene discovery; genomic medicine
BPA: Genomics; metabolomics; proteomics;
bioinformatics (health and non-health)
TIA: Translational services, biologics, cell therapies,
small molecules, pre-clinical testing and clinical trials;
support the ANZ Clinical Trials Registry
5. Focus of PHRN
PHRN’s focus is linked data:
Support national, state and territory data linkage units
Also secure file transfer, remote access and storage
We link administrative, clinical and other data,
including data from clinical trials, registries
and cohorts
6. Some health domain trends
Ongoing NCRIS investment via the four health
domain capabilities
Expanding and emerging platforms for clinical
research data
Opportunities eg for FAIR-er data