Our experience includes mechanical construction work for Eli Lilly and Company since the 1950s. We also provide conceptual design input, budget estimates, and realistic schedules for customers to confidently obtain project financing. We know that equally important as the work itself is the audit trail and validation document support required by the FDA (i.e. installation, operation, and performance qualification). Thus our projects are reliably performed without costly rework or regulatory shortcomings. We regularly provide project design input to ensure our biotech work meets both current and future customer needs. Furthermore, we manufacture/test custom process skid assemblies and provide local passivation services. Biotechnology/Pharmaceutical Technical Capabilities: cGMP manufacturing facilities   (including validated plants) Pilot plants Fermentation systems Ultra-high purity piping Equipment installations (i.e. bioreactors) Water-for-injection systems Waste-kill systems RO/DI water system installation/service Clean steam systems SIP/CIP systems Passivation Videoscope inspections Skid fabrications Medical gas systems Validation documentation support ASME coded tank repairs Instrumentation and controls