Well-planned and well-implemented investments strengthen industrial sector competitiveness. Sweco’s industry specialists have the full range of skills needed to drive projects from early studies to final realisation. The results are effective and resource-efficient production and a safe working environment.
Sweco offers consulting and design services for the pharmaceutical and medical device industry. In addition to design, we have comprehensive experience in life cycle management, approvals and quality assurance. We are familiar with Good Laboratory Practice (GLP), Current Good Manufacturing Practice (cGMP), Good Automated Manufacturing Practice (GAMP), Quality System Regulation (QSR), Medical Device Directive (MDD) and the requirements in the ISO 13485 standard.
We have worked together with several leading pharmaceutical and medical device companies in the Nordic countries. By combining our internal expertise, we can supply consulting and design services for all phases of investment projects from preplanning to the management, implementation planning and commissioning of the implementation project.