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Pharmaceutical Project Consulting and Design

Define the process, equipment, and facility requirements before procurement. NINGRUI supports pharmaceutical project consulting, feasibility studies, preliminary planning, and design coordination for new facilities and changes to existing operations.

Establish the Basis for Design

Feasibility and Preliminary Planning

Review the intended products, process route, production scale, site conditions, and project objectives. This work identifies the equipment and facility decisions that need to be resolved before detailed design or purchasing.

User Requirements Specification

Clarify the intended function, operating conditions, capacity, quality requirements, and acceptance expectations. An agreed user requirements specification (URS) gives the project team and equipment suppliers a common reference for design decisions.

Process and Layout Coordination

Review the process sequence, equipment arrangement, and material and personnel flows. Coordinate space, utility connections, access for operation and maintenance, and interfaces with the facility design.

Design Review and Handover

Coordinate design inputs and review comments with the relevant project participants. The agreed scope can include feasibility findings, a requirements document, process or layout proposals, and design review records.

Examples of facility layouts, 3D engineering models, and room design views

Work Through the Decisions in Sequence

  1. Share the product, process, location, and current project information.
  2. Define the consulting scope, required outputs, and responsibility for each design input.
  3. Review the planning and design proposals with the project stakeholders.
  4. Confirm the design basis and the information to carry into equipment procurement and subsequent project work.

The deliverables and depth of design are agreed for the project stage. Equipment procurement, site execution, and qualification activities need their own defined scopes.

Information to Prepare

Include the intended dosage forms or products, batch or annual capacity, process description, and available site drawings. Tell us which requirements are already approved, which decisions remain open, and the planned project milestones.

For projects with an existing URS, identify the equipment, layouts, or interfaces that need review.