Pharmaceutical Manufacturing Facility
A new plant for oral solid, liquid or semi-solid products, engineered from product and capacity to qualified operation.
Facility solutions
Each solution brings the relevant service disciplines together in the order a project needs them, from the first design decisions to qualified operation, engineered against the agreed project regulatory basis.
Solution index
A new plant for oral solid, liquid or semi-solid products, engineered from product and capacity to qualified operation.
Aseptic filling and terminally sterilised products, with contamination control designed into the building, air and utilities.
Sterile, non-sterile and hazardous compounding suites planned around the work, the room classification and the people.
Purified water and water for injection systems, from feed-water analysis to a qualified generation, storage and distribution loop.
Engineering path includes
Quality control, instrument and microbiology laboratories planned around the tests, the samples and the separation they need.
Facilities that handle hazardous or high-potency drugs, engineered to protect the product, the people and the environment.
Upgrading a running plant, suite or laboratory: from gap assessment to phased works and requalification.
Approach
The product, the process and the people define what the building must do before any discipline starts drawing.
Services are sequenced so every discipline works from the same design basis instead of correcting each other later.
Classification, pressure and containment follow the regulatory basis agreed for the project and the process risk.
Before the first layout, the project’s market, product, facility type and authority are agreed as a design basis. Read how that basis is set and what it controls.
Next step
Share the product type, the current stage and the main constraints. We will respond with a proposed scope and next steps.
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