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Focus on the Latest Regulatory and Risk Management Requirements for Medical Plastics

Here are the new, key regulatory and risk management requirements for plastics and additives used in medical devices, from design all the way to use.

How to Reduce Risk As Far As Possible

How to identify and analyze risk control options and implement those risk control measures that reduce risk as far as possible, without adversely affecting the benefit-risk ratio.

European Union Medical Device Regulation (EU MDR) and Risk Management — Reduce, Eliminate, Minimize, Remove or Avoid Risk?

Learn about the updated EU MDR's strong emphasis on safety and risk management.

Difference between Tollgate Reviews and Design Reviews

Tollgate Reviews and Design Reviews are both vital elements of product development, but many companies confuse the two. Here's the difference.

Integrating Medical Device Product Development, Design for Six Sigma and Quality Systems Requirements - Part 1

How to harmonize Quality System Requirements and DfSS with your New Product Development Process, Part 1

Integrating Medical Device Product Development, Design for Six Sigma and Quality Systems Requirements — Part 2

How to harmonize Quality System Requirements and DfSS with your New Product Development Process, Part 2

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