The American Society for Reproductive Medicine published a report that concludes preimplantation genetic testing for ...
The lifecycle of a medical device is under renewed regulatory and commercial scrutiny. Although lifetime expectations are not ...
The U.S. FDA has cleared Tessera Therapeutics Inc.’s IND application for TSRA-196, its lead in vivo gene editing therapy for α-1 antitrypsin deficiency (AATD). The Australian Human Research Ethics ...
The study shows that personalized medicine demands new competences that extend beyond traditional medical training.
Operational Resilience & Collaboration: Across every trend, the need for resilient, adaptable, and collaborative approaches ...
The engagement establishes a multi-phase framework to support AI enabled capital efficient development of Teverelix, a next generation GnRH antagonist, as a first in class market product for acute ...
This collaborative project with Montefiore Einstein’s Center for Bioethics aims to ensure that hospital ethics consultation and mediation practices are informed by the needs and values of the Bronx ...
Some of the reasons that friends and strangers alike blame victims for sexual assault may surprise you and make you very ...
The owner of a rescued lab dog considers if insights gleaned through animal research are enough to justify the practice.
FDA Clears IND Allowing Phase 2a Trial of NAV-240 in Hidradenitis Suppurativa to Begin Dosing in Q1 2026HREC Approval ...
Texas Oncology is now offering Texoma residents access to clinical trials for cancer treatment. Texas Oncology provides ...
Identifying copyright holders and response times are major challenges in COA licensing, causing delays in clinical trials. Clear documentation of copyright ownership and standardized response times ...