About AMICOM Analytics

Discover our vision, mission, and unwavering commitment to scientific excellence, regulatory compliance, and trust-based partnerships in analytical and biopharma services.

A Specialized CRO Built on Trust & Scientific Rigour

AMICOM Analytics is a specialized analytical and biopharma services organization supporting drug discovery, development, characterization, and regulatory submissions for peptides, biologics, and non-biological complex drugs (NBCDs).

We serve pharmaceutical, biotech, and biopharma companies across the drug development lifecycle — from early-stage discovery and method development through to regulatory submissions and commercial-stage testing.

Backed by strong scientific and quality expertise, we deliver end-to-end characterization ensuring compliance, integrity, and regulatory-ready documentation aligned with global GMP and GLP standards including WHO, CDSCO, FDA, and EMA.

ISO 9001:2015 Certified GMP Compliant GLP Compliant Audit-Ready
AMICOM Analytics - Analytical Laboratory
Swift Turnaround Fast, reliable results

Our Guiding Principles

Three core commitments that shape everything we do at AMICOM Analytics.

🤝

Customer Trust

AMICOM is dedicated to building a strong customer relationship based on Trust. Every engagement is an opportunity to demonstrate our integrity and scientific commitment.

🔬

Technical Excellence

We are committed to staying ahead of the curve by using the most advanced technology in our testing methods and instrumentation for specialty studies — including consultancy services.

Swift Turnaround

We are proud to provide swift turnaround of test results to all our valued customers, ensuring projects stay on track and timelines are met without compromise.

Our Quality Framework

A robust, audit-ready quality management framework aligned with global regulatory expectations.

🌍

Global GMP/GLP Compliance

Full compliance with global GMP and GLP expectations across all testing activities.

📋

Regulatory Documentation

Regulatory-aligned documentation and reporting ready for FDA, EMA, WHO, and CDSCO submissions.

🔗

Data Integrity & Traceability

Robust data integrity and traceability systems ensuring every data point is audit-trail secured.

🛡️

Audit-Ready QMS

A comprehensive, audit-ready quality management framework built to withstand any regulatory inspection.

🔒

Confidential Data Handling

Confidential and secure data handling protocols protecting customer intellectual property at all times.

📊

ISO 9001:2015 Certified

Internationally certified quality management system demonstrating our commitment to consistent quality.

Our Business Relationship Philosophy

Our business relation is built on ethics-driven, strong trust-based and transparent partnerships with long-term collaborations, scientific excellence, and regulatory compliance.

🔍

Understanding Scientific Needs

We take time to deeply understand each customer's unique analytical challenges, drug pipeline stage, and regulatory pathway requirements.

🤝

Trusted Partnership

We build transparent, ethics-driven, long-term collaborations ensuring scientific integrity and mutual growth throughout the engagement.

Quality Outcomes

Every project delivers regulatory-ready, scientifically robust results — meeting global quality standards and exceeding customer expectations.

Globally Aligned with Major Regulatory Standards

Our analytical and quality systems are built to meet the highest global regulatory expectations.

🌐
WHO GMP

World Health Organization

🇺🇸
US FDA

Food & Drug Administration

🇪🇺
EMA

European Medicines Agency

🇮🇳
CDSCO

Central Drugs Standard Control

📖
ICH Guidelines

Q2, Q3C, Q3D, Q6B & more

Get to Know Our Expert Team

Our leadership brings over 100 combined years of experience across analytical R&D, quality management, and biopharma sciences.

Meet Our Team Get in Touch