We are specialized in Pharma Turnkey Projects.

US Pharma provides end to end solutions for all your pharmaceutical formulation process & packaging needs. Our team of technical experts and professionals support your business right from the planning stage to commencing production. A one-stop solution in the pharmaceutical formulation industry for all your process and packaging worries i.e. tablet, capsule, liquid, oral, dry syrup, injectable and IV fluids, we equip your manufacturing line with the right systems to ensure maximum productivity. We employ the best technical knowhow to deliver effective sustainable results. From project planning, producing fabricating machinery to packaging materials for finished products, our aim is to meet all your project aspirations. Managing turnkey projects for some of the largest pharmaceutical manufacturing units; we design them as per WHO-GMP, USFDA, MHRA, TGA and cGMP norms & requirements. Our team provides valuable support and assistance even after project completion to ensure continued
prouction and minimal down times. Our cost-effective solutions improve overall project efficiency ultimately improving performance. Our ingenious designs and ethical business practices have helped us make our mark on the global markets as well.

Pharma Turnkey Project

Our Pharmaceutical Turnkey Solutions helps in setting up the entire processing plant.


Conception & Design Qualification

Conceptualization & Verification of the design to meet quality needs


Detailed Engineering

Studying every aspect of project development before starting construction


Validation Master Plan & SOP

Defining the areas and systems to be validated in the qualification phase


Equipment Construction & Proceurement

The phase of machine fabrication and equipment procurement


Factory Acceptance Test (FAT)

Evaluating the systems during and after assembly process that it is built as per design specifications


Shipping & Installation

Transferring and installing the systems to user site


Site Acceptance Test (SAT)

Testing after complete installation and final configuration to verify no damage occurred during shipment and installation


Validation Documentation (IQ/OQ/PQ Protocols)

Methods for demonstrating that equipment and system will offer a high degree of quality assurance consistently


Training, Commissioning & Start-up

Providing appropriate training to the staff and helping them set up the systems and initiate production phase



Procuring Licensors and Know How Transfers