Ensuring that your product is adequately labelled and the correct information is supplied is a requirement of medical device regulations (Note: for example see Annex 1 clause 13 of the Medical Device Directive 93/43/EEC).
QCS can provide guidance to ensure your products are labelled correctly for the markets that they are sold in, allowing you to have confidence that you have met the desired labelling and information requirements for you to finalise your packaging and product design.
QCS consultants have vast experience in compiling technical documentation to ensure that your labelling meets all requirements.
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