Pantec Biosolutions has received CE marking for its painless laser epidermal system (Please), which creates micropores in human skin prior to transdermal large-molecular-weight drug administration.
The audit is based on a conformity assessment procedure, and scrutinises product development and production documentation to ensure compliance to the Medical Device Directive (MDD).
Medical devices are required to bear a CE mark before they can be sold in member countries of the European Economic Area (EEA).