The pacproject team holds significant experience in design, development, specification and implementation of packaging concepts and packaging processes in the medical device industry. We know about the importance of verifications and validations during all phases of packaging development processes and packaging implementations. In the early phase of projects, we are able to identify the USER NEEDS of products and packaging to translate those into packaging benefits. We have the expertise to support in all matters of packaging (incl. planning and implementation of packaging machinery), as well as the preparation for compliance and support during the execution of audits (e.g. FDA, ANVISA, CE). We are familiar with the requirements of relevant standards and norms (e.g. MDD, DIN ISO 13485).