Awards are available for successful applicants from LMICs to cover the cost of their travel, accommodation and single-entry visa.
Meeting summary:
Artificial intelligence (AI) is increasingly being used in global health research but frameworks, policy and best practice for the ethical review and oversight of AI-enabled studies is currently lacking. The Forum will discuss how traditional research ethics regulatory frameworks have responded to the rapid advances in AI technology, and what changes are required, including to the role and responsibility of research ethics committees (RECs). It will explore the ethical challenges such as bias, privacy, data provenance and ownership, along with the need for transparency, accountability and engagement during the design and use of AI in global health research. To date, these discussions have predominantly taken place in high-income countries, and low- and middle-income country (LMIC) perspectives have been underrepresented. The Forum will consider the LMIC context where AI has the potential to address critical skills shortages and improve access to care, but where the ethical challenges are made harder due to existing disparities in infrastructure, knowledge and capacity. The Forum will take a multidisciplinary approach to explore how AI technology is being designed and used in health research, reflecting the range of actors involved in this space and the importance of computer scientists and technologists who apply AI for health to understand research ethics frameworks and considerations.
As part of the upcoming meeting, the GFBR is seeking case studies that bring attention to key ethical issues that have emerged regarding the use of AI in health research in LMIC settings and proposals to participate in a session on governance issues. The GFBR is also seeking participants to attend the meeting, with places awarded on a competitive basis.
Full details on how to apply are available on the GFBR website and the background paper provides further details on the meeting theme.
The deadline for applications is 17.00 CET on 17 June 2022.
The Stop
TB Partnership Working Group on New TB Vaccines (WGNV) and the National
Institute for Allergy and Infectious Diseases (NIAID)are
co-hosting a workshop on the topic of Recognition and Control of Mtb
Infected Cells: From Basics to the Clinic. This workshop is intended to address
the need for correlates and to identify platforms that measure recognition or
control of the infected cell - especially in humans - as identified in the EDCTP/AIGHD Global Roadmap for
Research and Development of New TB Vaccines and the Strategic Framework for
New TB Vaccines in the Stop TB Partnership Global Plan to End TB 2023 - 2030.
The overall goals of this workshop
are to:
The workshop format will be largely
discussion-based. Each session will have three short presentations that will
provide a high-level overview of key topics within the session theme, followed
by a discussion between the session chairs, speakers, and participants.
Click here
to view the programme and
speakers.
This workshop is free of charge and
open to any participants interested in this topic.
The International Society for Infectious Diseases (ISID) and the Swiss
Society for Infectious Diseases (SSI) are inviting applications for their joint
Infectious Diseases Research Fellowship Program. The purpose of this programme
is to support infectious disease physicians and scientists from under-resourced
countries through multidisciplinary clinical and laboratory training at a
select biomedical institution in Zurich, Switzerland. The one-year SSI/ISID
Fellowship programme is open to applicants who are 40 years or younger,
citizens and permanent residents of under-resourced countries or Eastern
Europe. The deadline for applications is 16 June 2023.
More information: https://na.eventscloud.com/eSites/748378/Homepage
The MRCT Center and Medable convened a multi-stakeholder task force to address ethical and regulatory opportunities and challenges related to Decentralized Clinical Trials (DCTs). Join them on June 20, from 10 - 11 AM ET, for a joint webinar entitled, "Ethical Review of Decentralized Clinical Trials (DCTs): Tools, Resources & Best Practices."
During the webinar, Barbara Bierer (MRCT Center), Pam Tenaerts
(Medable) and Leanne Madre (Medable) will present a framework, recommendations,
and tools organized around 3 DCT domains: People, Remote Data Collection, and
Data Oversight. Best practices for the ethical review, approval, and conduct of
DCTs will be provided.
Clinical trial stakeholders (IRB/ECs,
HRPP, sites, sponsors, investigators, and others) to register for the webinar here