ProMedic is pleased to announce the hire of Nichole Leahy-Glass. Nichole provides technical consulting services in Quality Management Systems. During her career, she has had several specific roles throughout the medical device life-cycle including Design Engineer, Quality Engineer, RA/QA Specialist, and Subject Matter Expert for Medical Device Start-ups and mid-sized companies. She has driven cohesion…
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FMMC Annual Symposium – ProMedic Exhibiting
The 2017 Florida Medical Device Symposium will be held May 8-9, 2017, at the Hilton Carillon Park in St. Petersburg. The symposium is Florida's premier event for medical device manufacturing firms, featuring nationally recognized speakers, expert panels on regulatory issues and industry trends, legislative updates and quality networking opportunities. The entire ProMedic team will be…
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Target-Controlled Infusions: Paths to Approval
Recently, Paul Dryden, President of ProMedic, authored an article regarding TCI. The purpose of this special article is to explore possible regulatory paths that could lead to TCI marketing clearance or approval by the FDA, permitting clinical use of this widely available technology in the United States. The article can be found HERE.
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District of Columbia Bar Admission
Congratulations to Matt Dryden on his recent Bar admission to the District of Columbia. Matt was sworn in the District of Columbia Court of Appeals on April 06, 2015.
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