Clean Room Validation & Project Management
Maintaining sterile and compliant environments is essential in pharmaceutical and healthcare manufacturing. Ethiqx provides clean room validation and project management services that ensure compliance with international standards while safeguarding quality and patient safety.
End-to-End Clean Room Design, Validation & Qualification
Designing, validating, and qualifying clean rooms for regulatory compliance.
ISO, GMP & International Standards Documentation
Ensuring adherence to the most stringent industry standards.
Project Execution & Lifecycle Management
Complete oversight from facility planning to operational readiness.
Key Features
- Certified validation expertise for pharma facilities.
- Global standard compliance (ISO, GMP, FDA, EU).
- Integrated project management for cost and time efficiency.
- Lifecycle support to maintain long-term operational excellence.