ISSCR News
ISSCR Statement on the Scientific and Therapeutic Value of Human Fetal Tissue Research
The International Society for Stem Cell Research (ISSCR), the largest professional organization of stem cell researchers from around the world, is concerned about a recent statement attributed to NIH that the agency will not renew research grants involving human fetal tissue (HFT), and that research with HFT is not conducted responsibly or transparently. In fact, research with HFT has been indispensable in advancing biomedicine and saving millions of lives, and it continues to play an essential role in accelerating research that benefits patients.
The ISSCR Partners with Nuffield Council on Bioethics to Compile Global Horizon Scan on Stem Cell Research
The International Society for Stem Cell Research (ISSCR) today announced a new partnership with the Nuffield Council on Bioethics (NCOB) to conduct an ambitious international horizon scan focused on the future of stem cell science and its ethical implications. The initiative will help signal and inform updates to the ISSCR Guidelines for Stem Cell Research and Clinical Translation and guide the Society’s broader public policy agenda.
Member Spotlight: Carolyn Sangokoya, MD, PhD
I enjoy problem-solving and designing molecular/genomic tools that help us to gain a new lens on biology. It's rewarding to do science with my team and see them gain skills, succeed, and find their niche.
The ISSCR Holds Inaugural Regulatory Meeting with Japan’s Pharmaceuticals and Medical Devices Agency and South Korea’s Ministry of Food and Drug Safety
On 7 November 2024, the International Society for Stem Cell Research (ISSCR) held its first meeting with Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) and Korea’s Ministry of Food and Drug Safety (MFDS). Held at PMDA’s Tokyo headquarters, the meeting brought together senior officials from PMDA and MFDS alongside ISSCR leaders based in Japan, Korea, and the United States.
At this inaugural meeting, participants convened to discuss key topics related to the:
1) manufacture of human Pluripotent Stem Cell (hPSC) banks as starting materials for allogeneic, PSC-based therapies, and
2) genetic assessment of hPSCs, 3) jurisdictional differences in guidelines for biological Ancillary Materials (AM).
The participants also had the opportunity to gain insights into the regulatory approaches of the PMDA and MFDS regarding PSC-based products.
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