HTCert defines clearly all conditions, rights and duties, as well as operating processes for assessment and certification of medical devices according to 93/42/EEC Directive.

A relevant document contains information on certificate maintenance, withdrawal or cancellation as well as handling of complaints, appeals and disputes.

Terms and conditions presented in this document govern the relation between HTCert and its clients and are applicable to all, unless exceptions are specifically agreed upon between the parties. In any case, exceptions cannot in any way concern the conformity assessment procedures according to which HTCert is required to operate.