Berman named vice president of clinical affairs at IlluminOss Medical

ILLUMINOSS MEDICAL has named Amy Orlick Berman vice president of clinical affairs.
ILLUMINOSS MEDICAL has named Amy Orlick Berman vice president of clinical affairs.

EAST PROVIDENCE – Amy Orlick Berman has been appointed IlluminOss Medical’s vice president of clinical affairs.
IlluminOss, a commercial stage medical-device company focused on minimally invasive orthopedic fracture repair, said in a news release that Berman brings almost two decades of clinical affairs experience and has extensive expertise leading global research programs from inception through product approval.
Berman will be responsible for the global clinical trial program at IlluminOss, including the U.S. Lightfix trial towards securing approval for the treatment of impeding and actual fractures of the humerus in patients with metastatic bone disease.
Berman previously was at Cordis, Johnson & Johnson for nearly 10 years where she held roles of increasing responsibility and oversaw a number of high-profile clinical research programs in the U.S., Europe and Japan.
“Ms. Berman has an impressive track record of fostering successful partnerships with the FDA, clinical research organizations, vendors and international scientific advisers to ensure approval and release of new medical devices and drug therapies,” Robert Rabiner, president and CEO of IlluminOss Medical, said in a statement. “We are pleased to make her a part of the IlluminOss Medical team and are confident she is the right fit to support the clinical trial efforts for the IlluminOss system.”
The IlluminOss system utilizes a light-curable polymer, contained within an expandable balloon catheter, resulting in an intramedullary patient-conforming implant to achieve almost instant bone stabilization for the treatment of complex fractures.
The system has proven successful in the treatment of more than 700 patients in Europe, where it is commercially available and has been in clinical use since 2010.
IlluminOss also now has conditional FDA approval for its first U.S. clinical trial.
“It’s a pivotal time for IlluminOss Medical and I am excited to be a part of the effort to validate its groundbreaking technology, which is expected to revolutionize fracture repair by providing a much less invasive option that can benefit both the orthopedic surgeon and their patient,” Berman said.

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