Workshop: Regulating Medical Software – What to expect in the coming year?

Thursday 14 November 2013 – 8:30-13:10

DITTA, the global voice for the diagnostic imaging, radiation therapy, healthcare IT, electromedical and radiopharmaceutical industry, is delighted to invite you to the Workshop: Regulating Medical Software – What to expect in the coming year?

Europe’s only event to exclusively focus on software used in medical practice…

• Latest updates on current medical software regulations and international comparison
• International and EU standards supporting regulations
• Complying with regulations
• Brief outlook into the future
• A unique opportunity to review latest regulatory and standardization developments in software used in medical practice

…with an international scope!

• Take advantage of the IMDRF meetings in Brussels to meet with regulators from 8 geographies (Australia, Brazil, Canada, China, EU, Japan, Russia, US)
• This workshop will be held the day after the IMDRF stakeholder forum 
• Speakers will be key international stakeholders including but not limited to regulators, notified bodies and industry representatives who are at the forefront of regulations and standards development for medical software

For the agenda and to register please click here