Workshop: Risk management according to DIN EN ISO 14971

Most international regulations for medical devices require manufacturers to implement risk management measures throughout the entire product life cycle of medical devices.

However, many companies find it difficult to define the product life cycle and implement suitable measures.

This workshop is intended to present a model for the product life cycle - or for activities in the design process and after market launch - and to show the various forms of risk management measures.

Examples will be given for most risk management measures and the concept of risk-based thinking when making decisions or finding solutions will be introduced.

Individual methods for risk identification and assessment are shown at a high level.

Speaker: Dr Marian Gransow

Costs:

• €50 for members
• €100 for non-members

The workshop will be held in English.

Register now and send an e-mail to katja.krempler@leap-up.com!