Clean and safe – the pure validation strategy

You want a clean and safe medical device in order to minimise patient risk and bring a perfect product to the market?

Then you should familiarise yourself with ISO 19227 and validate your cleaning process using this guideline and the associated guidelines.
With the upcoming webinar, we would like to give you an insight into ISO 19227 and guide you through the standard together in order to identify and evaluate the necessary and critical points.
We would like to identify the requirements and develop a validation strategy based on these requirements.
Furthermore, methods will be presented on how the requirements can be fulfilled and the evidence provided.
So if you would like to define your manufacturing process in terms of cleaning on a safe basis and thus guarantee your patients the greatest possible safety, then join our webinar.