Robust manufacturing processes, advanced technology and continuous training — so that safe, effective, high-quality product is the ordinary outcome, not the exception.
Manufacturing capabilities
World-class delivery
Everything below is standard practice at Graviti — written into batch records, trained on repeatedly and verified in every campaign.
Manufacturing under controlled environmental conditions (ISO Class-8 with temperature and RH control)
Line clearance performed before every manufacturing and packing run to prevent cross-contamination
Only qualified equipment, maintained under a rigorous programme of continuous operational control
All manufacturing and packing carried out to approved batch records for batch-to-batch consistency
Trained personnel operating in full compliance with current Good Manufacturing Practice guidelines
Thorough process validations, including cleaning validations and hold-time studies
Periodic and on-the-job training keeping teams current on cGMP requirements and best practice
Compression suite
Blister & band sealing
Specialty platforms
Laser drilling for osmotic controlled-release systems
Band sealing for moisture-sensitive capsules
Mini and micro tablet manufacturing
Precision functional and enteric coating
Modified-release matrix and multiparticulate platforms
Advanced oral solid drug delivery systems
Our facility runs laser drilling machines, band sealing machines, mini/micro tablet lines and precision coating — all aligned with USFDA standards and supported by an EIR. Planned expansions will further enhance capacity, operational efficiency and regulatory compliance.
From compression to container, one validated chain.
HPLC & GC analytics
Lab capabilities
Smart science, safer drugs
We are pioneers in pharmaceutical quality control with cutting-edge laboratory technologies, ensuring precision, compliance and reliability in every batch.
01
Comprehensive Analytical Expertise
In-depth QC analysis of raw materials, in-process samples and finished products using validated methodologies for consistency and efficacy.
Operating under strict compliance with USFDA, WHO-GMP and global regulatory standards.
04
Stability & Environmental Monitoring
Controlled stability chambers ensuring product efficacy and safety throughout shelf life.
05
Quality Control & Scientific Rigour
GLP practice, equipment qualification, calibration and robust data management.
Automation
Driving efficiency and compliance
We are investing heavily in robotics and futuristic technology, minimising human error, optimising processes and maintaining the highest standards of global regulatory compliance.
Robotic sample handling
Automated Equipment Cleaning & Maintenance
Ensuring high-level hygiene and repeatable compliance without manual variability.
Process Monitoring & Control Systems
Holding optimal manufacturing conditions continuously rather than checking them periodically.
Automated Line Clearance & Batch Processing
Reducing manual interventions and the error modes that come with them.
Real-Time Data Capture & Analysis
Turning plant data into better decisions and faster process optimisation.
Zero-intervention monitoring
By integrating automation into manufacturing and quality operations, we reduce human error, enhance process control and ensure regulatory compliance with global standards.
