Services

Commissioning Services

Services

Commissioning Services

Engineering and commissioning services ensure Good Engineering Practice (GEP) for biopharmaceutical and medical device companies building new plants, expanding or repurposing existing facilities, and commissioning / decommissioning equipment.

We commission virtually any biopharma, life sciences, or medical device manufacturing equipment and utilities required for greenfield or brownfield developments, including mechanical/HVAC, hold tanks, bioreactors, harvest systems, purification systems, architectural finishes, electrical components, lighting, plumbing, purified water, waste management, telecommunications, mixed gas systems, and much more.

We work with your engineering team to review designs and verify alignment as part of the integrated commissioning, qualification, and validation (CQV) process, increasing efficiencies, reducing cost, and ensuring cGMP compliance.

Life Sciences Commissioning and Qualification

Engineering and commissioning services ensure Good Engineering Practice (GEP) for biopharmaceutical and medical device companies building new plants, expanding or repurposing existing facilities, and commissioning / decommissioning equipment.

We commission virtually any biopharma, life sciences, or medical device manufacturing equipment and utilities required for greenfield or brownfield developments, including mechanical/HVAC, hold tanks, bioreactors, harvest systems, purification systems, architectural finishes, electrical components, lighting, plumbing, purified water, waste management, telecommunications, mixed gas systems, and much more.

We work with your engineering team to review designs and verify alignment as part of the integrated commissioning, qualification, and validation (CQV) process, increasing efficiencies, reducing cost, and ensuring cGMP compliance.

ICQ in Action

It had to be perfect, the first time.

“ICQ produced extraordinary results by maintaining 100% right-first-time metrics, helping to end the consent decree and completing all assigned scope one month early.”

Jim Rice
Former Sr. Director, Facilities & Engineering
Genzyme (now Sanofi)

Jim Rice
Former Sr. Director, Facilities & Engineering
Genzyme (now Sanofi)

Sanofi Genzyme (case study heading image)

Commissioning and Qualification for Life Sciences

  • Cycle Development (CIP and SIP)
  • Engineering Change Management
  • Engineering Test Plans
  • Start-up and Turnover
  • Shake Down Activities
  • Decommissioning
  • System Risk Assessments
  • Quality Risk Management (QRM)
  • System Boundaries
  • Project Planning and Execution

Commissioning and Qualification for Life Sciences

  • Cycle Development (CIP and SIP)
  • Engineering Change Management
  • Engineering Test Plans
  • Start-up and Turnover
  • Shake Down Activities
  • Decommissioning
  • System Risk Assessments
  • Quality Risk Management (QRM)
  • System Boundaries
  • Project Planning and Execution

How Can We Help You Get It Done Right?