Expertise

Pharma Manufacturing Operational Readiness

Expertise

Pharma Manufacturing Operational Readiness

We take a proactive, hands-on approach to pharmaceutical CQV project controls, so you don’t have to. With our deep pharma-specific expertise, we know what works. Proprietary, customized procedures and project templates allow us to spend less time on paperwork and more time operating and executing your CQV strategy.

Our Level 1–3 project schedules are fully integrated with milestone dates and construction deliverables, updated in real time, and shared with your quality and engineering teams for full transparency. What does this mean for you? We can quickly and accurately identify resource constraints before they happen, helping you adjust load management or schedules to avoid delays.

Pharma Manufacturing Operational Readiness

We take a proactive, hands-on approach to pharmaceutical CQV project controls, so you don’t have to. With our deep pharma-specific expertise, we know what works. Proprietary, customized procedures and project templates allow us to spend less time on paperwork and more time operating and executing your CQV strategy.

Our Level 1–3 project schedules are fully integrated with milestone dates and construction deliverables, updated in real time, and shared with your quality and engineering teams for full transparency. What does this mean for you? We can quickly and accurately identify resource constraints before they happen, helping you adjust load management or schedules to avoid delays.

$20MM

Planning Pays Off

Our pragmatic approaches and proactive planning methods help pharmaceutical companies complete projects ahead of schedule, often saving enough in overhead costs to pay for a majority of the capital project. For one client, we helped save $20MM by finishing the qualification project ahead of schedule.

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)

Pharmaceutical Expertise

  • Commissioning and qualification program development
  • Comprehensive validation planning and execution
  • Quality procedure audits
  • Quality management system alignment
  • Strategic gap assessments
  • Operational and inspection readiness
  • Project controls
  • Facility start-up
  • Change management processes
  • GMP facilities
  • CDMO facilities
  • Single-use facilities
Contact Your Local Rep

Contact Your Local Rep