We are experienced Trainers in Medical Device subjects, presenting on-site courses to regulators and industry in the US, Ireland, Scotland, Denmark, Sweden, Germany, Czech Republic, Brazil, and India.
Training in medical device quality systems and risk management can be provided on-site or via internet. We can provide customized training on medical device subjects such as ISO 13485, 21 CFR 820, ISO 14971, Process Validation, and IEC 60601-1 3rd Edition.
We have provided a number of webinars available at AAMI, Compliance On-line, and Global Compliance Panel.
Also we provide medical device risk management education at Virginia Tech in the graduate on-line program, Health Product Risk Management. More information at VT. We act as adjunct faculty in the medical device risk management course.
