Resources

Downloads &
Resources

Access our brochures, certificates, forms, and technical guides. All documents are available for download.

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Downloads

Company Brochures

PDF

AnalytiLab Company Brochure 2026

Comprehensive overview of all services, facilities, accreditations, and capabilities.

4.2 MB
PDF

E&L Studies Capability Brochure

Detailed brochure on Extractable & Leachable studies capabilities and regulatory expertise.

2.8 MB
PDF

Stability Studies Brochure

ICH stability studies capabilities, chamber specifications, and study types.

1.9 MB
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Pharmaceutical Testing Services Overview

Complete guide to pharmaceutical analytical testing services at AnalytiLab.

3.1 MB
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Downloads

Certificates & Accreditations

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NABL Accreditation Certificate (ISO 17025:2017)

Current NABL accreditation certificate with scope of accreditation.

0.8 MB
PDF

ISO 9001:2015 Certificate

Quality Management System certification by Bureau Veritas.

0.6 MB
PDF

USFDA Approval Letter

USFDA laboratory approval documentation.

1.2 MB
PDF

FDCA Gujarat Approval

State drug testing laboratory approval certificate.

0.5 MB
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Downloads

Forms & Templates

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Sample Submission Form

Standard form for submitting samples with required information for testing.

0.3 MB
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Quote Request Form

Request a testing quote with service requirements and timeline.

0.2 MB
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Non-Disclosure Agreement (NDA) Template

Standard NDA template for confidential testing projects.

0.4 MB
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Sample Condition Report Form

Form for documenting sample condition upon receipt.

0.2 MB
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Downloads

Technical Guides

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Stability Study Protocol Template (ICH Q1A)

Template stability protocol following ICH Q1A(R2) requirements.

1.1 MB
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E&L Study Design Guide

Guide to designing extractable and leachable studies per USP <1663>/<1664>.

1.5 MB
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ICH Q3D Elemental Impurity Risk Assessment Guide

Step-by-step guide for ICH Q3D risk assessment and testing strategy.

0.9 MB
PDF

Nitrosamine Risk Assessment Framework

Framework for nitrosamine risk assessment per FDA/EMA guidance.

1.3 MB
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Dissolution Method Development Guide

Guide to developing and validating dissolution methods per USP <711>.

0.8 MB
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IVRT/IVPT Study Design Guide

Comprehensive guide to designing IVRT and IVPT studies for topical products.

1.0 MB

Need a Custom Document?

Contact us for custom capability statements, audit questionnaires, or technical documentation.

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