Pharmaceutical
API, intermediates and GMP facilities engineered for compliance, containment and validation.
Engineering for Pharmaceutical Plants
Pharmaceutical manufacturing requires tight control of contamination, containment, environmental conditions, utilities and documentation. Cheminsight develops engineering solutions for API, intermediates and formulation facilities with the level of control required for regulated manufacturing.
What makes pharmaceutical demanding
cGMP compliance & validation burden
Cross-contamination & containment
Clean utilities (WFI, clean steam)
Regulatory documentation (US FDA, EU)
Pharmaceutical Engineering Solutions
- GMP Facility & Cleanroom Design
- Clean Utility Generation & Distribution
- Containment & HVAC Strategy
- Qualification & Validation Support
- Process & Equipment Engineering
- Multidisciplinary Detailed Engineering
Relevant services
Where we most often support pharmaceutical clients.
FEED
Detailed scope definition, P&IDs and a Class 3 estimate that lock the project basis ahead of detailed engineering and EPC.
ExploreMechanical Engineering
Static and rotating equipment design, specification and vendor engineering to international codes (ASME, TEMA, API).
ExploreInstrumentation & Control
Instrument selection, control philosophy, DCS/PLC architecture and safety systems (SIL) for reliable, safe operation.
ExploreEngineering for pharmaceutical?
Let’s talk about your process, your constraints and your goals.