Regulatory Approvals

Under the new guidance, only infants whose mothers test positive for hepatitis B or whose status is unknown will automatically receive the vaccine at birth.

The newly accredited program will deliver an extensive curriculum covering trauma and emergency management, sports injuries, joint replacement surgeries, and pediatric orthopedic care.

The Bendit17 microcatheter incorporates Bendit’s proprietary real-time 3D steering technology, which enables clinicians to maneuver the device more intuitively through complex vascular pathways.

Waskyra is specifically indicated for pediatric patients aged six months and older, as well as adults diagnosed with WAS who have a mutation in the WAS gene.

The newly approved toolbox serves as a sophisticated aid for healthcare professionals who need to identify signs of acute deterioration in their inpatient populations.

The test distinguishes between three distinct Bordetella species that cause different types of illness: B. pertussis, B. parapertussis and B. holmesii

The Zambia Medicines Regulatory Authority (ZAMRA) granted approval on November 4, 2025, completing its review in just 12 working days through an innovative regulatory pathway.

The therapy delivers the full-length human frataxin gene using a dual-administration approach that combines direct intradentate nucleus (IDN) injection with intravenous (IV) infusion.

This oral formulation offers a more convenient delivery method compared to intravenous treatments.