Jarvogen Website Sitemap
Explore all static pages, 12 specialized analytical testing service subroutes, facility dossiers, and client resources.
Main Navigation & Company Pages12 Links
Core & Leadership
Corporate overview, vision, mission, leadership, and operational team
- Home Page→
Precision Analytical Testing & cGLP Research Lab landing
- About Us→
Vision, Mission, Core Values & 2025 establishment
- Scientific Leadership→
Executive directors, Ph.D. chemists, and domain leads
- Contact Us→
Lab coordinates, location map, and technical inquiry desk
Laboratory & Infrastructure
Analytical instruments, equipment qualifications, and facility specifications
- Laboratory Facilities→
6 specialized labs with HPLC, LCMS/MS, GC-MS & ICP-MS
- Accreditations & Form 37→
FDCA Gujarat State Form 37 approval and statutory licensure
- Quality Assurance (QMS)→
cGLP compliance, ALCOA+ data integrity, and 21 CFR Part 11
Client Intake & Proposals
Sample submission, study requests, downloads, and documentation
- Request a Quote / RFP→
Custom study proposal, budget estimation, and turnaround
- Submit Sample Matrix→
Sample intake form, chain of custody, and LIMS barcoding
- Downloads & Literature→
Testing catalogs, instrument specs, and whitepapers
- Case Studies→
Recent analytical breakthroughs and regulatory studies
- Careers & Culture→
Opportunities for analytical chemists and QC scientists
Analytical Testing Services (12 Subroutes)12 Disciplines
Direct links to each individual analytical study and method validation route
Pharmaceutical Testing
Complete testing of APIs, formulations, excipients & finished products as per USP, EP, BP, IP, and ICH guidelines.
Analytical Method Development & Validation
Stability-indicating, residual solvent, dissolution, and cleaning validation methods per ICH/FDA/USP guidelines.
Stability Studies
ICH-compliant long-term, accelerated, and stressed stability studies with 24/7 monitored climatic chambers.
Extractable & Leachable (E&L) Studies
Assessment of drug-container interactions using LCMS/MS, GCMS, and ICPMS. Data accepted by US & EU regulators.
Elemental Impurity Testing
ICH Q3D-compliant testing of elemental impurities in APIs, drug products, and raw materials using ICP-OES and ICP-MS.
Nitrosamine / NDSRI Testing
Detection of nitrosamine traces in APIs and drug products using LC-MSMS. Compliant with FDA/EMA requirements.
IVRT & IVPT Studies
In-Vitro Release Testing and In-Vitro Permeation Testing for topical semi-solid products using Franz diffusion cells.
Chemical Analysis
Comprehensive wet chemistry and physico-chemical testing for pharmaceuticals, water, food, and industrial samples.
Water Analysis
Chemical, microbiological, and trace element testing of drinking water, purified water, WFI, and effluent samples.
Cleaning Method Validation
Validation that equipment is free from API residues and detergents between production batches, as per FDA cGMP guidelines.
Dissolution Profiling Studies
Comparative, multimedia, and method development dissolution studies for solid oral dosage forms per USP and FDA guidance.
Residual Solvent Testing
Headspace GC and direct injection GC methods for Class 1, 2, and 3 residual solvents in APIs and drug products.
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