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> Commissioning and Qualification
Our experienced PharmEng consultants strive to exceed your project goals and objectives. We understand the importance of developing the most effective and strategic approach that will meet your project schedules and budgets.
Our Subject Matter Experts (SME’s) thrive on implementing the latest industry strategies to meet your organizational and regulatory needs, as well as the current global regulatory requirements.
Our flexibility and project experiences range from the qualification of an individual piece of equipment to an entire facility.
Our PharmEng professionals have extensive experience in the development, implementation and execution of:
- Enhanced Detail Design Reviews – Design Qualification (DQ)
- Risk Management Tools
- Commissioning / Qualification / Validation Master Plans
- Project Management Tools (Budgeting, Scheduling, Tracking, Resource Planning)
- Facility / Utility System Commissioning Test Procedures
- Critical Utility System Qualification (IQ/OQ/PQ) Protocols
- Process Equipment and Process System Qualification (IQ/OQ/PQ) Protocols
- Controlled Temperature Units(IQ/OQ/PQ) Protocols
- Process Control Systems(IQ/OQ/PQ) Protocols
- Packaging Lines(IQ/OQ/PQ) Protocols
