Solar Energy
Offset production, cleanroom and facility loads while reducing exposure to rising utility costs.
Details →Industry
Energy solutions for bio-medical device manufacturing
Bio-medical device manufacturers need reliable power, controlled environments and efficient production. ecojiva delivers integrated energy solutions that protect your product, your profits and your future.
Medical Device Manufacturing
Key energy challenges
Controlled environments
Cleanrooms and controlled production areas require continuous HVAC, filtration and precise environmental conditions.
Reliability critical
Power interruptions can disrupt production, sensitive equipment, environmental controls and validated processes.
Energy intensive
Cleanrooms, HVAC, process equipment, compressed air and facility systems create significant electrical loads.
High demand & peaks
Production equipment, HVAC and facility systems can operate concurrently, creating costly peak demand.
Cost pressure
Energy-intensive production and environmental controls make electricity a significant and controllable operating cost in Minnesota, Massachusetts, Connecticut, Indiana and Michigan device clusters.
Regulatory compliance
FDA 21 CFR Part 820 QMSR requires documented quality systems and controlled manufacturing processes for finished medical devices.
Integrated solutions
ecojiva solutions will deliver results for your industry
Six solutions, engineered as one system and operated by ecoSEMS®, the AI platform that ties generation, storage and load control together.
Battery Storage
Reduce demand peaks from production equipment, HVAC, cleanrooms and other high-load processes.
Details →ecoSEMS® Controls
ecoSEMS® will monitor, optimize and document critical facility conditions to help support FDA 21 CFR Part 820 QMSR regulated operations.
Details →Sustainability
Lower energy costs and emissions while improving energy efficiency across manufacturing operations.
Details →FAQ
Questions from medical device manufacturing operators
How does ecoSEMS reduce cleanroom energy without affecting classification?
Cleanroom HVAC is often run at full design air-change rates around the clock. ecoSEMS coordinates air handlers, chillers and compressed air against production schedules and the utility peak window while holding pressure, particle and humidity limits, and logs every value for your QMSR records.
Is the QMSR transition relevant to energy systems?
The 2026 QMSR aligns 21 CFR Part 820 with ISO 13485 and keeps the emphasis on controlled processes and records. Continuous facility-condition logging from ecoSEMS supports the documentation your quality system needs.
