• Facility design-pharma/Biotech Formulation & API projects
• Finalization of Basis of Design (BOD), process sizing & process equipment sizing
• Basic Engineering- Concept Development, Layouts, Process Equipment Specifications & allied work
• Qualification of Process equipment & clean utility systems
• Cleaning Validation – VMP preparation, Documentation, Matrix development, associated training
• GMP-related training – both on-site and off-site
• GMP compliance Audits of API & Formulation facilities
• Technical Due diligence

Proficient

Org chart

Teams

Offices