#us fda

Collection of us fda news, found 8 news.

Indonesia takes three key steps to tackle cesium-137 contamination

Indonesia takes three key steps to tackle cesium-137 contamination

  • 7 hours ago

Indonesia’s National Food and Drug Authority (BPOM) said Monday it is taking three key steps to address ...

Task force to probe into cloves contaminated by Cs-137

Task force to probe into cloves contaminated by Cs-137

  • 3rd October 2025

The Cesium-137 Task Force will launch an investigation into reports of radioactive contamination in cloves, while also ...

Preliminary tests show no Cesium-137 contamination in clove products

Preliminary tests show no Cesium-137 contamination in clove products

  • 2nd October 2025

Environment Minister Hanif Faisol Nurofiq reported that preliminary findings from an inspection of a clove export ...

Bloomage Passes GMP Audit by South Korea's MFDS, Strengthening its Global Quality Assurance

Bloomage Passes GMP Audit by South Korea's MFDS, Strengthening its Global Quality Assurance

  • 9th April 2025

Bloomage, a global leader in hyaluronic acid and other bioactive substance innovations, has successfully passed the ...

Ministry-US FDA collaboration aims to ensure shrimp export quality

Ministry-US FDA collaboration aims to ensure shrimp export quality

  • 19th September 2022

The Marine Affairs and Fishery Ministry collaborates with the United States Food and Drug Association (FDA) in ...

Celltrion’s monoclonal antibody treatment regdanvimab, approved by the European Commission for the treatment of COVID-19

Celltrion’s monoclonal antibody treatment regdanvimab, approved by the European Commission for the treatment of COVID-19

  • 15th November 2021

Celltrion Group announced today that the European Commission (EC) has approved Regkirona (regdanvimab, CT-P59), one of ...

Celltrion receives CHMP positive opinion for regdanvimab (CT-P59) as one of the first monoclonal antibodies recommended as a treatment for COVID-19 by the CHMP

Celltrion receives CHMP positive opinion for regdanvimab (CT-P59) as one of the first monoclonal antibodies recommended as a treatment for COVID-19 by the CHMP

  • 12th November 2021

Celltrion Group announced today that the European Medicine’s Agency’s (EMA) Committee for Medicinal Products for ...

Neusoft releases NeuSight PET/CT for global markets

Neusoft releases NeuSight PET/CT for global markets

  • 19th January 2016

- Neusoft Medical Systems Co., Ltd. ("Neusoft Medical Systems") officially launched the NeuSight PET/CT for global ...