Designing or upgrading pharmaceutical facilities is more than an infrastructure project, it is a strategic investment requiring regulatory compliance, operational efficiency, and long-term scalability.
At ATP-CGPharm Group, we deliver tailor-made Facility & Process Engineering solutions for pharmaceutical, biotech, and life sciences companies.
From greenfield projects to site upgrades, we ensure your facility is optimized, compliant, and future-ready.
Our Expertise Covers
Facility Design & Optimization
Efficient, GMP-compliant manufacturing environments designed to maximize performance and streamline workflows.
Process Engineering & Automation
Advanced solutions improving efficiency, reducing costs, and ensuring consistent product quality.
GMP Compliance & Regulatory Consulting
Audits, gap analyses, and inspection readiness — with productivity always in focus.
Turnkey Project Delivery
From concept to commissioning, we manage the full lifecycle — integrating infrastructure, utilities, processes, and documentation seamlessly.
GxP-Compliant Facilities & Processes
Our services include :
• GxP Engineering
• Commissioning
• Qualification & Validation
• Quality Assurance & Quality Control
• Environmental Monitoring
We support pharmaceutical production sites, laboratories, warehousing, and R&D facilities across France, Switzerland, and internationally.
