Medical Device ISO 14971 Risk Management Training Services.

QSR 820 system counselling in the United States, BGMP system counselling in Brazil, JGMP system counselling in Japan, KGMP system counselling in Korea, UKCA QMS system counselling in the United Kingdom, FDA factory inspection counselling in the United States; and medical device system counselling in other countries.

MDSAP, Medical Device Single Audit Program MDSAP is a third party audit and assessment programme developed by the IMDRF organisation in 2014 to improve the safety and surveillance of medical devices for trade, resources and services. The aim is to achieve uniform recognition among different MDSAP member countries (TGA Australia, ANVISA Brazil, FDA USA, HC Canada, MHLW & PMDA Japan) through a single audit process.