cGLP & 21 CFR Part 11 Accredited Laboratory

Precision Testing & Scientific Analytical Services

Operated across 7 accredited analytical divisions in our 8,500 sq. ft. modern facility in Vapi, Gujarat. Delivering audit-proof, technically defensible test reports for pharmaceutical, water, environmental, food, and industrial manufacturers.

7
Specialized Divisions
Pharma, Water, Air, Food & more
8,500
Sq. Ft. Testing Lab
On NH-48 in Vapi, Gujarat
21 CFR
Part 11 Compliant
Electronic audit trails & QA sign-off
24-48h
Express Turnaround
Available for urgent batch releases
Comprehensive Testing Portfolio

Our 7 Testing & Analysis Divisions

Every division operates under dedicated standard operating procedures (SOPs), qualified instrumentation, and certified reference standards.

Pharmaceutical & Formulation Testing
cGLP • 21 CFR Part 11 Compliant

Pharmaceutical & Formulation Testing

Comprehensive Defensible Analytical Testing for APIs, Excipients & Finished Formulations

Satvam Research delivers cGLP and 21 CFR Part 11 compliant analytical testing for pharmaceutical manufacturers across Gujarat, Maharashtra, and pan-India. Operating an 8,500 sq. ft. laboratory on NH-48 in Vapi, our pharmaceutical testing covers Active Pharmaceutical Ingredients (APIs), excipients, pellets, tablets, capsules, injectables, and medical devices strictly per IP, BP, USP, EP, JP, and ICH guidelines.

Key Test Scope:
Assay, Purity & Related Substances
Residual Solvents & Volatile Impurities
Trace Elemental Impurities (ICH Q3D)
In-Vitro Dissolution & Physical Release
TAT: 5 to 7 Business Days
•Indian Pharmacopoeia (IP), United States Pharmacopeia (USP <621>, <232>, <467>, <711>)
Water, Wastewater & Environmental Water Testing
IS 10500:2012 • BIS & CPCB Norms

Water, Wastewater & Environmental Water Testing

Precision Chemical, Trace Metal & Microbiological Evaluation for Industrial, Drinking & Effluent Streams

Satvam Research operates an advanced water and environmental analytical division in Vapi, Gujarat, delivering full physicochemical, toxic heavy metal, and microbiological testing. We test drinking water per IS 10500:2012, packaged natural mineral/drinking water (IS 13428 / IS 14543), pharmaceutical Purified Water / WFI, and industrial wastewater (ETP/STP effluent) per CPCB and GPCB pollution control standards.

Key Test Scope:
Potable & Drinking Water Analysis (IS 10500:2012)
Industrial Effluent & Wastewater (ETP / STP)
Pharmaceutical Process Water (Purified Water & WFI)
Borewell, Groundwater & Boiler Feed Water
TAT: 3 to 5 Business Days
•Bureau of Indian Standards: IS 10500:2012 (Drinking Water), IS 14543:2018 (Packaged Drinking Water)
Environmental Monitoring & Industrial Hygiene
MoEF&CC Aligned • CPCB Guidelines

Environmental Monitoring & Industrial Hygiene

Field Sampling & Laboratory Analysis for Ambient Air, Stack Emissions, Workplace Hygiene & Noise

Satvam Research provides certified environmental monitoring and industrial hygiene services across industrial manufacturing zones in Gujarat and Maharashtra. Equipped with calibrated high-volume air samplers, stack monitoring kits, flue gas analyzers, and Class-1 sound level meters, we measure ambient air quality (NAAQS), stationary emission sources (DG sets, boilers, scrubbers), workplace chemical exposure, and noise levels.

Key Test Scope:
Ambient Air Quality Monitoring (AAQM)
Stationary Stack & Flue Gas Emission Testing
Workplace Air Quality & Industrial Hygiene
Noise Level Monitoring
TAT: 4 to 6 Business Days after field sampling completion
•National Ambient Air Quality Standards (NAAQS - CPCB Notification 2009), The Air (Prevention and Control of Pollution) Act, 1981
Food, Agriculture & Dietary Supplement Testing
FSSAI Aligned • Nutritional & Contaminant Profiling

Food, Agriculture & Dietary Supplement Testing

Rigorous Chemical, Nutritional, Heavy Metal & Pathogen Testing for Food & Agricultural Commodities

Satvam Research operates an advanced food and agricultural testing division evaluating raw agricultural products, processed foods, edible oils, spices, dairy products, dietary supplements, and nutraceuticals. Our testing strictly adheres to Food Safety and Standards Authority of India (FSSAI) regulations, Agmark, and international export standards, providing verified nutritional profiling, pesticide screening, and toxic heavy metal quantification.

Key Test Scope:
Nutritional Labeling & Proximate Analysis
Toxic Trace Elements & Heavy Metals
Pesticide Residues & Agricultural Contaminants
Mycotoxins, Aflatoxins & Preservatives
TAT: 4 to 6 Business Days
•Food Safety and Standards Act, 2006 (FSSAI Regulations), FSSAI Food Safety and Standards (Contaminants, Toxins and Residues) Regulations
Agrochemical & Pesticide Testing (CRO Services)
CIPAC Guidelines • CIB&RC Standards

Agrochemical & Pesticide Testing (CRO Services)

Contract Research & Quality Control Testing for Technical Grade Actives & Formulated Crop Protection Products

Satvam Research delivers dedicated contract testing and analytical research (CRO) services for agrochemical manufacturers, pesticide formulators, and technical active ingredient producers. Located in the chemical industrial corridor of Vapi, Gujarat, we perform active content assay (HPLC/GC), complete CIPAC physicochemical characterization, accelerated storage stability (CIPAC MT 46.3), 5-batch analysis support, and container compatibility studies aligned with Central Insecticides Board & Registration Committee (CIB&RC) standards.

Key Test Scope:
Active Ingredient (AI) Quantification & Purity Assay
CIPAC Physical-Chemical Characterization
Storage Stability & Shelf-Life Studies
Packaging & Container Compatibility
TAT: 5 to 7 Business Days (Chemical assay); 20 to 25 Business Days (Accelerated stability studies)
•Collaborative International Pesticides Analytical Council (CIPAC) Methods, Central Insecticides Board & Registration Committee (CIB&RC) Guidelines
Equipment Calibration & Metrology Services
ISO/IEC 17025 Aligned • NABL Traceable Standards

Equipment Calibration & Metrology Services

Precision Calibration, Thermal Validation & Metrology Solutions for Analytical & Industrial Equipment

Satvam Research provides precision calibration and thermal validation services for analytical laboratories, pharmaceutical manufacturing units, chemical plants, and testing facilities across Vapi, Daman, Silvassa, and Gujarat. Operating under strict ISO/IEC 17025 principles with NABL-traceable reference standards, our metrology team calibrates analytical balances, thermal chambers, UV-Vis spectrophotometers, volumetric glassware, and digital instrumentation.

Key Test Scope:
Thermal Validation & Temperature-Humidity Mapping
Mass Metrology & Weighing Equipment
Optical & Spectrophotometric Metrology
Volumetric Glassware & Liquid Handling
TAT: On-site validation: 1 to 2 Days; Glassware calibration: 3 to 4 Business Days
•ISO/IEC 17025:2017 (General requirements for the competence of testing and calibration laboratories), NABL Specific Criteria for Calibration Laboratories
Global Export & Regulatory Release Testing (CRIA / NAFDAC Aligned)
Export Release • CRIA & NAFDAC Aligned

Global Export & Regulatory Release Testing (CRIA / NAFDAC Aligned)

Authorized Analytical Dossier Testing, CRIA Compliance & Commercial Consignment Release for Global Markets

Satvam Research provides comprehensive export consignment testing, commercial batch release verification, and regulatory dossier support for pharmaceutical, chemical, cosmetic, and food exporters. We specialize in testing required for the Clean Report of Inspection & Analysis (CRIA) for exports to Nigeria (NAFDAC guidelines), GCC health ministries, ASEAN countries, and international regulatory bodies.

Key Test Scope:
Export Consignment Commercial Batch Release
NAFDAC & CRIA Testing for Nigeria Exports
Export Regulatory Dossier & Stability Support
Export Food, Beverage & Chemical Consignments
TAT: 3 to 5 Business Days
•National Agency for Food and Drug Administration and Control (NAFDAC) Nigeria Guidelines, Clean Report of Inspection and Analysis (CRIA) Scheme
Standard Operating Procedure

Sample Testing Workflow in 4 Steps

From sample login to authorized Certificate of Analysis (CoA) dispatch

01

Sample Receipt & Login

Samples logged into LIMS with unique tracking barcode, condition check, and temperature verification.

02

Validated Analysis

Analysis executed strictly per validated method or compendial monograph on qualified instrumentation.

03

Dual QA Review

Senior analyst calculation check and independent Quality Assurance officer data integrity audit.

04

CoA Authorization

Tamper-evident Certificate of Analysis (CoA) issued electronically and dispatched with original raw data packets.

Frequently Asked Questions

Frequently Asked Questions

What testing and analytical divisions are operated by Satvam Research?

Satvam Research operates 7 specialized analytical testing divisions at our 8,500 sq. ft. cGLP facility in Vapi: (1) Pharmaceutical & API Testing, (2) Water, Wastewater & Environmental Water, (3) Ambient Air & Stack Environmental Monitoring, (4) Food, Agriculture & Nutritional Testing, (5) Agrochemical & Pesticide Formulation CRO Testing, (6) Equipment Calibration & Metrology, and (7) Global Export & Regulatory Release Testing (CRIA / NAFDAC aligned).

How does Satvam Research ensure data integrity in analytical reports?

All chromatographic instrumentation (Shimadzu HPLC Prominence-i, Shimadzu Brevis GC-2050 Headspace, LabIndia Dual-View ICP-OES) operates under 21 CFR Part 11 computerized data management. All analyses feature immutable electronic audit trails, automated password aging, role-based operator controls, and dual-level QA authorization.

How can industrial clients submit samples for testing from Vapi, Daman, Surat, or Mumbai?

Our logistics coordinators provide express on-site sample collection across Vapi GIDC, Sarigam, Umbergaon, Daman, Silvassa, and Valsad. For clients in Mumbai, Surat, Ankleshwar, and Ahmedabad, we accept direct cold-chain courier drop-offs and express highway shipments directly at our NH-48 laboratory.

What are the standard turnaround times for laboratory test reports?

Standard testing turnaround ranges between 3 to 7 business days depending on test complexity. For urgent commercial batch clearance, customs hold consignments, and critical manufacturing audits, expedited 24 to 48-hour rush processing is available.

Schedule Your Testing & Protocol Review

Contact our laboratory in Vapi to discuss test specifications, request express sample collection, or book a facility audit.