Responsive Validation & Commissioning
Joulé manages all aspects of commissioning and validation for pharmaceutical, biotech, and other regulated manufacturing processes and equipment. Our services not only ensure quality, functionality, and performance, they also reduce costs and headaches.
Extensive Validation Experience
We know our business. Joulé’s staff validation experts offer significant industry insight and understanding of GxP requirements, for both newly-constructed and existing facilities. From SOP development and custom IQ, OQ, and PQ documentation, to full plan execution, you can count on quality workmanship. To meet FDA requirements, we also deliver complete documentation packages.
Core Validation Services
- Standard Operating Procedure (SOP) and Protocol Development
- Analytical and Manufacturing Equipment Commissioning and Validation
- Process, Facility and Utility Equipment Commissioning and Validation
- Metrology and Calibration Program Development
- Preventive Maintenance Program Development
Simply put, Joulé excels at equipment and process validation. And because we offer a full suite of integrated equipment services, you’ll never have to go anywhere else.
Employers & Clients
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