MedTech Europe have requested feedback on the relevant standards applicable to IVD packaging that would influence the minimisation of packaging. This includes both mandatory labelling requirements and specifications of packaging.
Therefore, please provide your input on the following two points relating to MedTech Europe’s draft paper:
- Do you agree with the approach of “considering “contact sensitive packaging” as one ‘most common packaging type” for which the medtech specific standards given further on in the documents should be suggested to apply?
- Could you kindly complete the table of ‘relevant standards to keep in consideration’, and in particular the final column on ‘sector specificities of the standard to be taken into account in the further proceedings on Article 10’
The deadline for feedback is Friday 8 August 2025, EOD.
Please email responses to regulatory@bivda.org.uk. These will be collated and sent to MedTech Europe.
