•Pharmaceutical Plant Design & Setup – End-to-end facility planning and execution.

•Detailed Project Report (DPR) – Comprehensive report for project feasibility.

•Drug Manufacturing License – Assistance in obtaining regulatory approvals.

•Regulatory Compliance Implementation – Adherence to Schedule M, USFDA, and MHRA and Other standards.

•WHO GMP Compliance – Ensuring Good Manufacturing Practices for global standards.

•Sustainable & Scalable Design – Future-ready and eco-friendly facility planning.

•Civil AutoCAD Drawings – Detailed structural designs for optimal facility layout

•Plumbing & HVAC Drawings – Efficient water, air, and climate control systems.

•Electrical Drawings – Energy efficient planning for power distribution.

•Machine GA Drawings – Strategic machinery placement for smooth workflow.

•Man & Material Flow Drawing – Efficient Man and Material movement planning for high productivity with quality.

•Quality System Management – Implementation and maintenance of GMP-compliant quality systems.

•Regulatory Audit Preparation & Compliance – Assistance in meeting global regulatory standards.

•Regulatory Query Response Support – Expert guidance for handling technical queries.

•Drug Master File (DMF) Preparation – Product-wise documentation for regulatory submissions.

•Staff Training – Preliminary guidance and training for routine quality compliance.