Risk Management

A risk management process covering all product realization processes starting from design and development is very important to ensure product safety and regulatory compliance.

ISO 14971 is the basis for a medical device risk management process. Special processes like software, packaging, sterilization validations has to be included to the risk management processes starting from the planning phase. ConsulTeam experts provide consultancy services covering all product realization processes in line with ISO 14971 requirements.

For detailed information you may contact us or read the current post.