We help you design pharmaceutical facilities that comply with international standards, from design concepts and space planning to the integration of cleanroom systems, HVAC, water systems, and automation. As an experienced consultant, we provide precise, efficient, and GMP-compliant design services to support the smooth operation of your pharmaceutical production processes.

This SOP serves as a structured working guideline for consulting teams in handling pharmaceutical facility design projects efficiently, systematically, and in compliance with regulations such as CPOB/GMP.

In general, this SOP includes:

1. Project Initiation - Receiving client requests, preparing proposals, and conducting kick-off meetings.

2. Site Survey & Data Collection - Conducting site surveys, analyzing requirements, and reviewing applicable regulations.

3. Conceptual Design - Developing initial layout designs and obtaining client approval.

4. Detailed Design - Preparing complete technical designs for cleanrooms, HVAC systems, water systems, utilities, and automation systems.

5. Finalization & Documentation - Delivering final drawings, reports, and qualification documentation.

6. Project Closure - Conducting project evaluation with the client and documenting lessons learned.

The main objective is to ensure design quality, regulatory compliance, and timely execution at every stage of the project.