№ files_lp_3_process_7_062614
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Official funding call specifications outlining eligibility criteria, scope, budget, timelines, and administrative requirements for research proposals under the ICMR component of the GACD research programme.
Funding agency:
Indian Council of Medical Research (ICMR)
Funding agency website:
https://www.icmr.gov.in/
Open date:
30 November 2021
Final application deadline:
31 May 2022
Co-funding requirement:
Proposals must include Indian investigators meeting ICMR eligibility criteria and co-Principal Investigator(s) eligible under at least one other GACD funding agency
Total budget available:
INR 30,000,000 (equivalent to USD 420,000)
Maximum amount per project:
Up to INR 15,000,000
Approximate number of projects:
Up to 3
Permitted project length:
3 years
Geographic scope:
Projects conducted in India
Target population:
Young people aged 10–24 years
Intervention scope:
Non-structural, non-pharmaceutical, non-biomedical device interventions
Eligible institutions:
Institutions with a valid SIRO certificate issued by DSIR
Principal Investigator requirement:
Must be based at an eligible institution
Contact person:
Dr Tanvir Kaur
Contact email:
[email protected]
Thematic focus:
Lifelong health improvement and potential intergenerational impacts among youth
Document type:
Funding call specifications
Price: 8 / 10 USD
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Funding agency:
Canadian Institutes of Health Research (CIHR)
Program:
GACD Grant Programme
Status:
Planned participation; applications not yet open
Open date:
TBD
Pre-proposal deadline:
TBD
Final application deadline:
31 May 2022
Total budget available:
CAD 10,000,000
Maximum amount per grant:
CAD 400,000 per year for up to 5 years (maximum CAD 2,000,000 per grant)
Expected number of grants:
At least 5
Permitted project length:
5 years
Geographical focus:
Low- and middle-income countries (LMICs) and disadvantaged populations in Canada
Research focus:
Implementation research using a life course approach to reduce non-communicable disease (NCD) risk
Eligible applicants:
Canadian-LMIC research teams with required representation from LMIC institutions and knowledge users
Additional requirements:
Inclusion of decision makers or policy makers from LMICs; specific requirements for research involving disadvantaged or Indigenous populations
Pre-proposal requirement:
Mandatory
Co-funding:
Possible for proposals involving investigators from other participating GACD countries
Contact:
CIHR Contact Centre ([email protected]
Note:
)
Document type:
Funding call summary
Issuing organization:
Canadian Institutes of Health Research (CIHR)
Year:
2017–2019
Country:
Australia
Population:
Aboriginal and Torres Strait Islander pregnant women
Health Focus:
Smoking cessation during pregnancy
Programme Name:
ICAN QUIT in Pregnancy (Indigenous Counselling and Nicotine)
Project Team:
Gillian S. Gould; Yael Bar-Zeev; Michelle Bovill; Billie Bonevski; Maree Gruppetta; ICAN QUIT in Pregnancy Pilot Group
Setting:
Aboriginal Medical Services (AMSs) in New South Wales, Queensland, and South Australia
Study Design:
Step-wedge cluster randomised pilot trial
Sample Size:
22 pregnant women; 50 health providers
Intervention Components:
Webinar-based provider training; culturally tailored educational resources (“Wingadhan Birrang”); free oral Nicotine Replacement Therapy
Theoretical Framework:
Behaviour Change Wheel (BCW); COM-B model; Theoretical Domains Framework (TDF)
Stakeholder Engagement:
Community-based participatory research; Stakeholder and Consumer Aboriginal Advisory Panel (SCAAP)
Primary Outcomes:
Feasibility; acceptability; provider knowledge and attitudes; validated smoking abstinence at 12 weeks (13.6%)
Implementation Sites:
Six Aboriginal Medical Services
Expansion Initiative:
SISTAQUIT™ (Supporting Indigenous Smokers To Assist Quitting) cluster randomised controlled trial
Source Type:
Implementation science case study
Advertisement Number:
03/2023
Advertisement Date:
24/02/2023
Position:
Junior Research Fellow
Project Title:
Fabrication and testing of Lower Limb Prosthesis for Transtibial Amputee using Biocomposites with Energy Restoring Capability
Funding Agency:
Indian Council of Medical Research (ICMR), Government of India
Project File Number:
ICMR/2021/14663
Implementing Institution:
NIT Uttarakhand
Department:
Department of Mechanical Engineering
Principal Investigator:
Dr. Pawan Kumar Rakesh
Number of Posts:
01
Essential Qualifications:
B.Tech and M.E/M.Tech. or equivalent degree in Mechanical Engineering/Biomedical subjects with minimum 1st class (or 60% if class not specified) or 6.75 CGPA
Fellowship:
Rs. 31,000 per month + HRA
Interview Type:
Walk-In-Interview
Interview Date and Time:
28th February, 2023 at 11 AM
Interview Venue:
Department of Mechanical Engineering, NIT Uttarakhand, Srinagar Garhwal - 246174
Application Procedure:
Submission of application form with originals and self-attested photocopies at interview; advance copy via email to [email protected]
Duration of Post:
Initially one year, extendable up to project duration based on performance
Nature of Appointment:
Temporary, project-based
Additional Conditions:
No TA/DA for attending interview; eligibility subject to reporting time and document verification; option to register for Ph.D. subject to institute requirements
Year:
2022
Region / City:
India
Topic:
Funding opportunities for GACD research projects
Document Type:
Information sheet
Organization:
Indian Council of Medical Research (ICMR)
Author:
Dr Tanvir Kaur
Target Audience:
Researchers applying for funding
Effective Period:
2022–2023
Approval Date:
30 November 2022
Deadline for Letter of Intent:
15 March 2023
Final Application Deadline:
7 June 2023
Funding Amount:
INR 30,000,000 (USD 420,000)
Maximum Project Funding:
INR 15,000,000
Number of Projects Funded:
Up to 3
Project Duration:
3 years
Co-funding Requirements:
Co-funding agencies involved
Eligibility:
Institutions with valid SIRO certificate from DSIR
Location Requirements:
Projects must take place in India
Ethical Guidance:
Refer to co-funding agency’s guidelines
Contact Information:
Dr Tanvir Kaur – [email protected]
Year:
2026
Region / city:
Not specified
Subject:
Financial assistance / bursary application
Document type:
Application form
Organization / institution:
UKZN (University of KwaZulu-Natal)
Author:
Not specified
Target audience:
Undergraduate and postgraduate students
Validity period:
2026 academic year
Approval date:
Not specified
Amendment date:
Not specified
Note:
Year
Context description:
This document is a form for individuals applying for various roles, including external assessors and subject matter experts within the MTM organization, with sections for experience validation and necessary qualifications.
Year:
2017
Region / City:
Jackson, MS, Houston, TX
Topic:
Government Contracting, Solicitation, Acquisition
Document Type:
Contract Solicitation Form
Organization:
Department of Veterans Affairs
Author:
Department of Veterans Affairs
Target Audience:
Contractors, Offerors
Period of Validity:
Not specified
Approval Date:
09-03-2017
Amendment Date:
Not specified
Note:
Year
Region / City:
Seattle
Subject:
Legal proceedings
Document type:
Court notice
Organization / Institution:
King County Superior Court
Target audience:
Attorneys, legal professionals, involved parties
Context:
Court notice for hearing date and procedural requirements in Seattle, Washington.
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Year:
[]
Region / City:
[]
Subject:
Convertible Loan Agreement
Document Type:
Agreement
Organization / Institution:
[]
Author:
[]
Target Audience:
[]
Period of Effect:
[]
Approval Date:
[]
Amendment Date:
[]
Year:
2025
Note:
Region / City
Theme:
Business Software / Presentation Software
Document Type:
Lesson Plan
Author:
Glenda Liddell-White
Target Audience:
Students
Period of Validity:
April 14 – 18, 2025
Contextual Description:
A lesson plan for teaching students how to create and manage professional presentations using Microsoft PowerPoint.
Year:
2021
Region / city:
United States
Topic:
Business communication
Document type:
Template
Organization / institution:
Not specified
Author:
Dusty Davidson
Target audience:
CEOs, business leaders, teams
Effective period:
Weekly
Approval date:
Not specified
Amendment date:
Not specified
Year:
2005
Region / City:
[Not specified]
Topic:
Legal Procedure
Document Type:
Legal Form
Organization / Institution:
[Not specified]
Author:
[Not specified]
Target Audience:
Legal professionals, parties involved in legal proceedings
Period of Validity:
[Not specified]
Approval Date:
[Not specified]
Date of Amendments:
[Not specified]
Year:
[Date]
Region / City:
[Location]
Subject:
Legal document, affidavit
Document Type:
Affidavit
Author:
[Name of the Deponent]
Target Audience:
Legal professionals, courts
Period of Validity:
N/A
Approval Date:
[Date]
Date of Amendments:
[Date]
Year:
[Not provided]
Region / City:
South Australia
Subject:
Affidavit
Document Type:
Legal Form
Agency / Institution:
Court of South Australia
Author:
[Not provided]
Target Audience:
Legal professionals, parties involved in court cases
Period of validity:
[Not provided]
Approval Date:
[Not provided]
Amendment Date:
[Not provided]
Year:
2025
Region / City:
Not specified
Topic:
Nuclear Regulatory Commission Inspection and Performance Indicators
Document Type:
Inspection Manual
Organization / Institution:
U.S. Nuclear Regulatory Commission
Author:
U.S. Nuclear Regulatory Commission
Target Audience:
NRC Inspectors, Licensees of Nuclear Facilities
Period of validity:
From January 1, 2025
Approval Date:
Not specified
Date of changes:
Not specified
Note:
Year
Document Type:
BIM Execution Plan
Articles Included:
Project Information, Designated Delivery Milestones, Software Requirements, Data Security, Modeling Protocols, Model Management, Levels of Development, Reliance Authorization, Model Identification, Other BIM Provisions, Exhibits and Attachments
Document type:
Explanatory memorandum
Legal act concerned:
Regulation (EU) 2023/1115
Policy area:
Environment and climate policy
Subject matter:
Deforestation-free supply chains
Commodities covered:
Cattle, cocoa, coffee, oil palm, rubber, soya, wood
Proposed change:
Postponement of date of application
Length of postponement:
12 months
Original application date:
30 December 2024
Legal basis:
Article 192(1) TFEU
EU institution:
European Commission
Geographical scope:
European Union
Stakeholders concerned:
Member States, operators, traders, third countries
Related strategies:
European Green Deal, EU Biodiversity Strategy for 2030, Farm to Fork Strategy
Regulatory impact assessment:
Carried out for Regulation (EU) 2023/1115
Budgetary implications:
As set out in the legislative financial statement attached to Regulation (EU) 2023/1115
Year:
2024
Region / City:
Singapore
Topic:
Family Law, Court Procedures
Document Type:
Legal Form
Organization:
Family Court
Author:
Family Justice Courts
Target Audience:
Legal practitioners, applicants, respondents involved in family dissolution matters
Effective Period:
2024
Approval Date:
Not specified
Modification Date:
Not specified