Nicomac Europe supplies highly customizable cleanrooms for pharmaceutical and microbiological labs, compliant with the norms USP <797>, USP <800>, cGMP, FDA, NAPRA and adequate for outsourcing facilities 503B.
Our service includes:
Our company follows the client in all the project phases, ensuring assistance even when it comes to validation actions.
Our widespread network of aftersales assistance can answer 24/7 and ensures quick interventions, reducing to the minimum the risks of a production stop.
Nicomac Europe cleanroom features
Nicomac Europe design, realizes and installs cleanrooms for laboratories capable of answering to every need of sterile (injected drugs, given intravenously or directly on the eyes) and non-sterile (oral drugs or topical treatments) compounding, complying with air cleanness standards from ISO 5 to ISO 8. In the case of microbiological analysis, in a medical, molecular or other field, our controlled contsmination environments follow from ISO 5 to ISO 7 standards.
Nicomac Europe laboratories cleanrooms ensure flexible solutions, adaptable to any size and efficient thanks to the modular system, the exclusive Hipharma design, HVAC and filtering (HEPA e ULPA) systems and to the professionalism and experience of its specialized consultants and technicians. Our company can supply solutions for the conservation of dangerous materials and air down flow systems.
Discover all the application fields of our cleanrooms
Nicomac Certified Quality
Nicomac Europe is international leader in the cleanroom sector and in the coating and granulation systems. TIts productive excellence and the reliability of its services are recognized in 65 Countries in the world, in which were completed over 1.800 projects. The North-american market is given to the partner Nicos Group, part of the Nicomac Group, for the distribution and installation.