Industrial plant design & construction


We support you from feasibility study to validation, while providing multi-technical coordination for customized or complex installations, in new-build or renovation projects, and carrying out retrospective retrofits.

Ludovic Savary

Senior Project Manager

Laboratories and pilot plants

The design of laboratories andpilot plants was the basis for the creation of Added Value Engineering in 2005. Since 2007, this activity has expanded to the scale of production and manufacturing workshops. Our services can start with feasibility studies feasibility studies and accompany you right through to commissioning and validation.

Every year, numerous customers place their trust in us for the design and construction of their facilities, because we bring a capacity to integrate user needs as well as all legal standards and directives, and do multi-technical coordination.

We have built R&D and QC laboratories for chemistry, biology, medical, materials science and criminal analysis. We have also built laboratories for highly active substances (HPAPI), including cytotoxic compounds.

AVe has set up pilot units in the fine chemicals, base chemicals, pharmaceuticals and food sectors, and has also set up a pilot unit for highly active substances (HPAPI).


Production equipment and production lines

On a production scale, we have numerous achievements in basic and fine chemicals (dosing/reaction/liquid-solid separation/drying/packaging), as well as in the food industry (production, storage and packaging of flavors, chocolate, coffee and dairy products) and microelectronics (gas and liquid dosing, production machine integration).

Our specific know-how in production plant design enables us to design and build customized and/or complex installations. We are experienced in both new installations and renovations (revampings), and have been called upon to carry out retrospective retrofits.

Quality and standards


For biotechnology or pharmacology projects, we implement equipment design that takes into account your quality requirements. Throughout the project, we formalize activities in validated documents. We follow all FDA/Swissmedic requirements, applying ISPE guidelines, and are also able to propose customized approaches if required.