All pharmaceutical and medical products must be manufactured under controlled conditions in compliance with statutory limit values. Compliance with these specified limit values ​​must be continuously monitored. The requirements for the conditions depend on the product to be produced. There are therefore different clean room classes which are defined in EN ISO 14644 or in the GMP guidelines Annex 1. We offer you turnkey cleanroom concept solutions from a single source. Planning, dimensioning, execution and validation including all documentation are completely included in our offer.