Advanced Solutions for Pharma, Life Science & F&B Industries
Built for industries that can’t afford compromise
In industries where compliance failures halt production, quality issues damage brand trust, and inefficiencies eat into margins, operational excellence is not optional. Utthunga works with pharmaceutical, life sciences, and food and beverage organizations to compress validation timelines, reduce operating costs through automation, accelerate regulatory readiness, and build manufacturing systems that scale without disruption.
Our approach connects process engineering, automation, and digital systems to remove inefficiencies, improve product consistency, and ensure quality at every step—delivering the infrastructure that lets you move faster, operate leaner, and scale smarter while turning regulatory challenges into competitive advantages.
Our Core Competencies
Conduct comprehensive audits aligned with GxP, FDA, EMA, FSSAI, and ICH guidelines to identify non-conformances, improve documentation practices, and ensure inspection readiness across laboratories, production facilities, and supply chains.
Implement SCADA, MES, and LIMS-integrated automation for cleanrooms, bioreactors, filling lines, and analytical labs to enhance throughput, ensure data integrity, and maintain compliance with 21 CFR Part 11 and EU Annex 11.
Enable digital transformation through electronic batch records, cloud-enabled validation platforms, and real-time traceability systems that uphold ALCOA+ principles and meet global standards including PIC/S and WHO requirements.
Provide expert consultation across regulatory submissions, market authorization, QMS implementation, and product lifecycle management—supporting compliance with FDA, MHRA, FSSAI, WHO, and CDSCO for pharmaceuticals, biologics, medical devices, and food products.
Design, optimize, and qualify GMP-compliant production lines and HVAC infrastructure, and utilities for sterile manufacturing and food processing—leveraging cleanroom design, process validation, hygiene zoning, and contamination control protocols.
Deliver turnkey EPCC projects for laboratories and manufacturing plants—covering design, procurement, clean utility systems, and commissioning—ensuring cGMP alignment, validation, and audit-readiness from day one.
Develop dynamic simulation models for aseptic processing, HVAC zoning, and deviation scenarios to support equipment validation, operator training, and performance optimization in GxP-regulated environments.
Lab & Manufacturing Automation Solutions
Digitalization for Data Integrity & Traceability
Specialized Regulatory Consultation Services
Process Engineering for GMP Environments
Simulation for Validation & Operator Training
Our Integrated Solutions for Pharma, Life Science & F&B
Benefits of Our Pharma, Life Science & F&B Solutions
Accelerated Development & Regulatory Approval
Our automation-enabled workflows streamline clinical operations, regulatory submissions, and eCTD workflows—accelerating time-to-market for pharmaceuticals, biologics, medical devices, and novel food ingredients while ensuring full regulatory alignment.
Compliance Excellence Across GxP Environments
We enable consistent compliance with global regulatory standards like FDA, EMA, FSSAI, ICH, and WHO through digital validation systems, continuous audit readiness, and robust GxP/GHP-aligned documentation and reporting frameworks.
Optimized GMP Operations & Quality Control
Our integrated solutions enhance batch consistency, deviation management, and real-time monitoring—minimizing manual errors and enabling scalable, efficient operations across manufacturing, quality control, and supply chain management.