Built on Integrity.
Engineered for Analytical Excellence.
Founded to bridge the critical gap between regulatory stringency and rapid commercial release, Satvam Research Private Limited operates an 8,500 sq. ft. modern testing facility in Vapi, Gujarat, delivering technically valid, 21 CFR Part 11 compliant data for life sciences innovators.
Our Vision & Mission
Setting higher standards for analytical reliability and regulatory compliance in South Gujarat and beyond
Our Vision
“To be a globally recognized leader in pharmaceutical and chemical testing, ensuring the highest standards of scientific quality, safety, and reproducible data integrity for the benefit of public health.”
Our Mission
To deliver accurate, technically valid, and timely analytical testing services by pairing qualified scientific talent with qualified chromatography and spectroscopy instrumentation operating strictly under 21 CFR Part 11 and cGLP governance.
8,500 Sq. Ft. Laboratory Architecture
Engineered with segregated testing zones to prevent cross-contamination and ensure maximum workflow efficiency
Chromatography & Trace Analysis Suite
Equipped with Shimadzu Prominence HPLC (UV/PDA), Shimadzu GC-2010 Pro with Headspace autosampler, and Lab India ICP-OES 2100 for sub-ppb heavy metals screening.
Cleanroom Microbiology Suite (Class 10,000)
Environmentally controlled cleanroom facility with calibrated biosafety cabinets, incubators, and autoclaves for Microbial Limit Tests (MLT), bioburden, and pathogen screening.
Stability & Photostability Center
Walk-in and reach-in environmental chambers mapped across ICH conditions (25°C/60% RH, 30°C/65% RH, 40°C/75% RH) with multi-point 24/7 continuous datalogging.
Dedicated Water Testing Suite
Standalone laboratory zone specifically configured for testing potable, packaged, and purified industrial water per Bureau of Indian Standards IS: 10500:2012.
Wet Chemistry & Physical Characterization
Complete instrumentation suite for dissolution profiling (USP App I/II), Karl Fischer moisture titration, FTIR spectral fingerprinting, and particle size evaluation.
Controlled Sample Inward & Archive Suite
Segregated sample storage with dedicated temperature zones (2°C–8°C, ambient, -20°C) and automated barcoded chain-of-custody tracking from receipt to CoA release.
Why Partner With Satvam Research?
The scientific rigor and governance framework protecting your batches
Scientific Rigor & Accuracy
Every test protocol is conducted with uncompromised precision and strict adherence to global compendial monographs (IP, BP, USP, EP, JP) and validated internal methodologies.
21 CFR Part 11 Data Integrity
Multi-tiered user access controls, unalterable electronic audit trails, automated password expiration, and secure local server archiving guarantee zero data tampering.
Regulatory Alignment & Defensibility
Quality systems designed around cGLP, ISO/IEC 17025:2017, NABL criteria, Drugs & Cosmetics Act 1940, and stringent international regulatory expectations.
Qualified Scientific Talent
Staffed by certified analytical chemists, microbiologists, and regulatory experts trained to resolve complex testing bottlenecks and deliver dependable turnarounds.
Strategic Location on National Highway 48
Positioned in South Gujarat's chemical & pharmaceutical manufacturing belt with direct connectivity to Western India
Strategic Highway Connectivity
Situated directly on National Highway 48, providing seamless logistics and same-day sample pickup across Mumbai, Surat, Bharuch, Vadodara, and Ahmedabad.
Proximity to Mega Industrial Hubs
Directly connected to Vapi GIDC, Sarigam GIDC, Umbergaon GIDC, Pardi GIDC, Gundlav GIDC, Daman Industrial Area, and Silvassa Industrial Area—one of India's largest industrial corridors.
Trained Scientific Talent Pool
Availability of qualified pharmaceutical chemists, microbiologists, and regulatory experts experienced with USFDA, WHO, and EU compliance workflows.
Robust Industrial Infrastructure
Continuous power, high-grade water, secure sample warehousing, and cold-chain storage facilities supporting strict turnaround times.
Ready to verify our laboratory capabilities first-hand?
We invite QA heads, regulatory affairs managers, and procurement directors to schedule an on-site facility audit or request sample pickup from our Vapi laboratory.