Latest FDA Stories
Cost-effective, high-quality production of API using microbial expression systems BOONTON, N.J., Feb.
Pennsylvania Senator Robert Casey says that the U.S.
The report’s publication follows the issuance of two power morcellator warnings from the FDA regarding the potential for morcellation to spread undetected uterine cancers. New
A recent analysis of 2014 Form 483s issued to devicemakers found that purchasing control violations were up 17% over 2013. Join FDAnews on Feb.
VALLEY COTTAGE, N.Y., Feb.
FDA approves Cohera's TissuGlu® Surgical Adhesive, supporting the elimination of drains in abdominoplasty procedures PITTSBURGH, Feb.
Compliance with IEC 62304 is required for all electromedical devices where basic safety is dependent on software or firmware.
On January 28, 2015, Harper’s Bazaar Magazine’s website posted an article about UltraShape, the ultrasound device FDA approved for reducing belly fat. Dr.
SAN DIEGO, Feb.
The filing of this morcellator lawsuit comes just months after the FDA warned that uterine morcellation should be avoided in the majority of women who require hysterectomy and fibroid removal
- A political dynamiter.