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Environmental Discipline
FDCA Form 37 Approved21 CFR Part 11 Compliant
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Water Analysis

Chemical, microbiological, and trace element testing of drinking water, purified water, WFI, and effluent samples.

Potable WaterWFIEffluentMicrobial
Turnaround Time5–7 working days
Water TypesDrinking, Purified, WFI, Effluent
StandardsUSP, BIS, WHO, EPA
Parameters50+ chemical & microbial
● Lab Capacity ActiveForm 37 Certified

Study Protocol Support

Direct access to analytical specialists for study design, method validation, and turnaround timelines.

Submit Sample MatrixDownload Service Spec Sheet
Direct Technical Desk:+91 76240 54108
Service Scope & Regulatory Framework

Rigorous Scientific Execution Built for Global Regulatory Dossiers

Jarvogen provides comprehensive water testing services for pharmaceutical-grade water (Purified Water, WFI), drinking water, process water, and effluent samples. Our testing covers chemical purity, microbiological safety, trace element analysis, and TOC determination, compliant with pharmacopoeial and environmental standards.

Compendial Standards & Regulatory Alignment:
✓ BIS (IS 10500)✓ WHO Guidelines✓ USP <645>✓ USP <643>✓ EPA✓ CPCB
Dual-Analyst Review

100% 4-eye verification of all chromatograms, integrations, and calculations before CoA generation.

ALCOA+ Data Integrity

Direct electronic data capture with immutable audit trails, restricted rights, and disaster backups.

Technical SpecificationscGLP Compliant

Turnaround Time5–7 working days
Water TypesDrinking, Purified, WFI, Effluent
StandardsUSP, BIS, WHO, EPA
Parameters50+ chemical & microbial
Quality Credentials
FDCA Gujarat Form 37ICH Compliant (Q1–Q14)21 CFR Part 11
Key Analytical Capabilities

What's Covered in the Testing Scope

Comprehensive assay, stability, and characterization endpoints validated to global pharmacopoeial standards.

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Purified water testing (USP <645>)Executed with validated SOPs and full raw data audit trails.
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Water for injection (WFI) testingExecuted with validated SOPs and full raw data audit trails.
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Drinking water (BIS IS 10500)Executed with validated SOPs and full raw data audit trails.
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TOC determination (USP <643>)Executed with validated SOPs and full raw data audit trails.
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Conductivity and pHExecuted with validated SOPs and full raw data audit trails.
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Heavy metals and trace elementsExecuted with validated SOPs and full raw data audit trails.
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Microbiological testing (TVC, coliforms)Executed with validated SOPs and full raw data audit trails.
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Endotoxin in pharmaceutical waterExecuted with validated SOPs and full raw data audit trails.
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Effluent and wastewater analysisExecuted with validated SOPs and full raw data audit trails.
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Nitrates, nitrites, fluorides, chloridesExecuted with validated SOPs and full raw data audit trails.
Qualified Laboratory Infrastructure

Validated Instrumentation & Data Systems

All instruments operate with full IQ/OQ/PQ qualification, automated audit trails, and 21 CFR Part 11 software packages.

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TOC Analyzer

Total organic carbon in purified water/WFI

IQ/OQ/PQ QualifiedALCOA+ Audit Trail
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Ion Chromatography

Anion and cation analysis

IQ/OQ/PQ QualifiedALCOA+ Audit Trail
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ICP-OES

Trace metals in water

IQ/OQ/PQ QualifiedALCOA+ Audit Trail
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AAS

Heavy metals in water samples

IQ/OQ/PQ QualifiedALCOA+ Audit Trail
Study Execution Lifecycle

How We Execute Your Study

Standardized 4-stage laboratory workflow ensuring traceability from sample intake to CoA release.

01
Stage 01

Sample Collection & Preservation

Water samples collected in appropriate containers with preservation as required.

02
Stage 02

Physical & Chemical Testing

pH, conductivity, TOC, and chemical parameters tested immediately.

03
Stage 03

Trace Element & Microbial Testing

ICP-OES for metals; microbiological testing in cleanroom environment.

04
Stage 04

Compliance Report

Results compared against BIS/WHO/USP limits; compliance report issued.

Scientific Questions & Answers

Technical FAQs

Standard testing is delivered in 5–7 working days. Expedited priority slots are available upon request with dedicated instrument reservations and expedited QC review.
Ready for Sample Testing?

Initiate Your Water Analysis Study

Submit your sample matrix or request a pre-study analytical protocol discussion with our senior scientists today.

Schedule Scientific Consultation
Cross-Discipline Solutions

Related Analytical Services

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Pharmaceutical Testing

Complete testing of APIs, formulations, excipients & finished products as per USP, EP, BP, IP, and ICH guidelines.

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Analytical Method Development & Validation

Stability-indicating, residual solvent, dissolution, and cleaning validation methods per ICH/FDA/USP guidelines.

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Stability Studies

ICH-compliant long-term, accelerated, and stressed stability studies with 24/7 monitored climatic chambers.

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