Publicity and promotion of funded projects in media and at professional meetings.Parts and shipping required to adopt new technology and.Expenses related to the development, hosting, and management of online projects.Subcontracting to outsource creative work, events organization, or other work that requires expertise the imaging community does not provide.Salary for the Imaging Scientist or additional personnel to help with the project or to assist running their imaging core to allow the Imaging Scientist dedicated time for the funded project.Example metrics include the number of researchers using a new technology, the number of participants for a training or a workshop, or the number of attendees at a meeting. Grantees will work towards completion of a collaborative project and specify metrics that will be used to evaluate the project’s success. Selected projects will be funded for two years (24 months). Training and education: Organizing in-person or online courses on imaging for biomedical researchers and train-the-trainers programs, implementing and adapting new media for training and education, and developing teaching materials or courses for researchers who are starting their careers as imaging scientists.websites or coordinating organizations) that enable collaborations in the imaging community and online platforms to exchange methods, tools, and protocols. Building capacity: Developing frameworks (e.g.Validation and dissemination of new imaging technologies: Collaboration between technology developers and imaging scientists to test and validate new imaging systems and/or to adopt new imaging platforms at imaging cores.Cross-institutional applications are strongly encouraged.įunds can be requested in one or more of the categories below: “Imaging Scientists” might be engineers, physicists, mathematicians, computer scientists, or biologists who have focused on technology development in either light or electron microscopy, medical imaging, or data analysis fields, or work at the interface of biology, microscopy hardware, and imaging software at an imaging core facility. Project proposals must be submitted by an imaging scientist who is a faculty member (research or tenure track) with at least one Co-PI and no more than ten Co-PIs. To broaden the impact of these efforts, the Chan Zuckerberg Initiative (CZI) invites applications for new and existing collaborative projects to reduce imaging ecosystem fragmentation and accelerate the spread and adoption of technologies, methods, or training resources. While the quickly growing worldwide imaging community is beginning to collaborate to develop new technologies and resources that can benefit the broader ecosystem, many of these projects are supported by dedicated volunteers and operated without dedicated funding. This project is due to commence in May 2021 and will run until December 2021.Imaging ecosystems are highly fragmented, which slows the spread and adoption of imaging hardware and software technologies, methods, and data. Together, we will work through the CTR timelines and processes for review of a select number of clinical trials ahead of the application of the CTR later in 2021. It aims to enable national readiness for and facilitate a smooth national transition to, the CTR by replicating in, so far as possible, the coordinated processes necessary to deliver a ‘single national opinion’ from the two authorities.Īs part the collaborative project, the HPRA and the NREC-CT, supported by the National Office, will work closely with a small group of volunteer, academic and industry sponsors conducting trials in Ireland. The National Collaboration Project is jointly run by the HPRA and the National Office over a six-month period. The scope of the NREC for review of Clinical Trials of Medicinal Products (NREC-CT) will be based on the requirements of the EU CTR. The CTR represents significant change to the way sponsors submit clinical trial documentation, and how the Health Products Regulatory Authority (HPRA) and the newly launched National Research Ethics Committees (NRECs) review and approve clinical trials in Ireland. This in turn will harmonise submission and assessment processes, improve collaboration and information-sharing, increase transparency, and further improve standards of safety for research participants – collectively fostering an environment that is more favourable for conducting clinical trials across the EU. The CTR will harmonise the assessment and supervision processes for clinical trials throughout the EU, via a Clinical Trials Information System (CTIS). The way clinical trials are conducted across the European Union will undergo major changes under the Clinical Trials Regulation (CTR) – due to be applied in early 2022.
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