About AMICOM Analytics
Discover our vision, mission, and unwavering commitment to scientific excellence, regulatory compliance, and trust-based partnerships in analytical and biopharma services.
Discover our vision, mission, and unwavering commitment to scientific excellence, regulatory compliance, and trust-based partnerships in analytical and biopharma services.
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.
Three core commitments that shape everything we do at AMICOM Analytics.
AMICOM is dedicated to building a strong customer relationship based on Trust. Every engagement is an opportunity to demonstrate our integrity and scientific commitment.
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.
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.
A robust, audit-ready quality management framework aligned with global regulatory expectations.
Full compliance with global GMP and GLP expectations across all testing activities.
Regulatory-aligned documentation and reporting ready for FDA, EMA, WHO, and CDSCO submissions.
Robust data integrity and traceability systems ensuring every data point is audit-trail secured.
A comprehensive, audit-ready quality management framework built to withstand any regulatory inspection.
Confidential and secure data handling protocols protecting customer intellectual property at all times.
Internationally certified quality management system demonstrating our commitment to consistent quality.
Our business relation is built on ethics-driven, strong trust-based and transparent partnerships with long-term collaborations, scientific excellence, and regulatory compliance.
We take time to deeply understand each customer's unique analytical challenges, drug pipeline stage, and regulatory pathway requirements.
We build transparent, ethics-driven, long-term collaborations ensuring scientific integrity and mutual growth throughout the engagement.
Every project delivers regulatory-ready, scientifically robust results — meeting global quality standards and exceeding customer expectations.
Our analytical and quality systems are built to meet the highest global regulatory expectations.
World Health Organization
Food & Drug Administration
European Medicines Agency
Central Drugs Standard Control
Q2, Q3C, Q3D, Q6B & more
Our leadership brings over 100 combined years of experience across analytical R&D, quality management, and biopharma sciences.