Cleanrooms
The topic is planned and the article has not been written yet. Nothing on this page is published technical guidance.
This article will examine how the facility requirements for sterile and nonsterile compounding differ: room classification, primary engineering controls, ante and buffer rooms, pressure relationships, and cleaning provisions. It will also cover where the two can share space and where they must stay separate.
If this question is live on your project, you do not need to wait for the article. Tell us about the facility and we can discuss it directly.
01Cleanrooms
In preparationThis article will examine how pressure cascades set the direction of air movement between rooms, when a cascade protects the product and when it protects people, and how airlocks, door leakage, and room tightness affect it. It will also explain why differential pressure targets are defined per project rather than copied between facilities.
02Cleanrooms
In preparationThis article will examine what environmental monitoring covers in controlled areas: nonviable particles, viable air and surface sampling, differential pressure, temperature, and humidity. It will also look at how monitoring points are selected, how alarms and data logging are planned, and why these decisions belong in design.
03Facility Planning
In preparationThis article will examine the first decisions behind a new pharmaceutical plant: product portfolio and dosage forms, sterile or nonsterile scope, capacity and shift assumptions, site constraints, and the regulatory framework of the target markets. It will also explain how these inputs become a brief that design can build on.
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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