Accepting samples — Chhatral, Gujarat

HPLC and GC analysis for pharmaceutical manufacturers

Method development and validation through routine batch release.

Validated methods, reviewed data and submission-ready documentation for formulation and API manufacturers. Send us a specification and we will confirm feasibility, timeline and cost.
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Techniques on site
HPLC (UV/Vis, DAD) GC (FID, Headspace) Dissolution (Basket/Paddle) FTIR UV-Vis Spectrophotometry Titrimetry & Potentiometry
Modern analytical testing laboratory equipped with high performance liquid chromatography HPLC instruments
Method development & validation
Developed, challenged, documented.
Batch release & COA
Full supporting data with every report.
NABL accreditation in progress.
Data Integrity
Audit trails, raw data preservation and two-tier technical review on every test.
Predictable Lead Times
Committed turnaround times agreed before testing begins.
Regulatory Ready
Protocols, COAs and reports formatted for regulatory submission.
Direct Access
Speak directly with the analyst running your method.
About the lab

An analytical partner for pharmaceutical development and release testing

The Analytical Lab is an independent analytical testing facility based in Chhatral, Gujarat, working with pharmaceutical manufacturers and R&D teams. Our work covers method development and validation through to routine batch analysis, with the protocols, reports and raw data needed for regulatory submission.

HPLC & GC specialization Dedicated instrumentation for assay, purity, related substances and residual solvents.
Method validation to ICH Q2(R1) Specificity, linearity, accuracy, precision, LOD/LOQ and robustness.
Chhatral industrial location Serving formulation and API units across Ahmedabad, Kadi, Kalol and Mehsana.
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Quality control testing laboratory with high precision analytical equipment and dual analyst verification
Analytical chemist conducting method validation and sample analysis
Laboratory sample preparation for HPLC and GC mass spectrometry testing
Our services

Two service lines, one quality standard

R&D support for products in development, and routine analysis for products in production. Both run on the same documented methods and review process.

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Method development & validation

Custom HPLC & GC method development for novel APIs, complex formulations and stability studies.

  • Method development & optimization
  • ICH Q2(R1) validation protocols & execution
  • Forced degradation & stability-indicating method design
  • Method transfer to client / commercial site
Method development details →

Routine analysis & COA release

Rapid, reliable testing for raw materials, finished products and in-process samples with full data packets.

  • Raw material & excipient testing
  • Finished product release testing (COA)
  • Assay, related substances & dissolution
  • Residual solvent analysis by GC-headspace
Routine testing details →
Why The Analytical Lab

Precision is a process, not a promise

Every result we issue is traceable to a written method, a calibrated instrument and a second review. That is what makes data usable in a submission.

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01
Protocol-driven analytical execution

Every study follows an approved written protocol before bench work begins.

02
Traceable reference standards & instruments

All standards tracked; instruments calibrated against certified references.

03
Independent secondary data review

Raw data and chromatograms reviewed by a senior analyst prior to release.

04
Audit-ready documentation packages

Reports include method details, sample logs, chromatograms and calculation sheets.

Who we work with

Industries & applications

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Formulation Manufacturers

Finished product release, dissolution profiling and stability testing for solid oral and liquid dosage forms.

API Manufacturers

Purity profiling, assay, related substances and residual solvents for active pharmaceutical ingredients.

Pharma R&D Teams

Analytical support during early development, formulation screening and method feasibility.

Excipient & Chemical Suppliers

Raw material identification, purity testing and COA verification against monograph standards.

How we work

From enquiry to final report

See the full process →
01

Discuss requirements

Scope, specification and timeline agreed in writing.

02

Sample submission

Samples logged with reference standards and documentation.

03

Analysis

Testing performed against the approved method and protocol.

04

Review & reporting

Data reviewed, then issued as COA or full study report.

05

Ongoing support

Queries, repeat testing and method transfer as needed.

Have an analytical requirement?

Send us your specification or method and we will confirm feasibility, timeline and cost.

Request a Quote or call +91 72038 58401