APIsand R&Ds
We are dedicated to delivering niche Active Pharmaceutical Ingredients (APIs), impurities, and reference standards with a strong focus on quality, compliance, and reliability. Through strategic global partnerships, we provide high-value, low-volume APIs and analytical consultancy services to pharmaceutical companies, research organizations, and healthcare innovators.
Core Operations
End-to-end support for discovery, development, and compliance.
APIs — Active Pharmaceutical Ingredients
High-quality specialty APIs with analytical support and regulatory traceability.
Impurity Standards
Certified impurity & reference standards to support method development and validation.
Analytical Consultancy
Method development, validation (ICH Q2), E&L, nitrosamines, stability and elemental impurity support.
Consultancy Services
On-site investigations, QC operational excellence, inspection readiness and accreditation support.
Custom Synthesis
API route scouting, impurity synthesis and pilot-scale support for R&D and regulatory batches.
Outsourcing Solutions
Vendor qualification, audited global sourcing and compliant supply chain management.
R&D & Innovation
Pioneering scalable, green synthetic routes and integrated analytical solutions for future therapies.
Reference Standards
Working/reference standards and certified materials to support analytical qualification and regulatory filings.
Why Dr. Sahu's Laboratories?
Quality & Compliance You Can Trust
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ICH-aligned Methods
Q2(R1) validation, Q3D elemental impurities, nitrosamines. -
GLP Mindset
Data integrity, traceability & audit-ready documentation. -
ISO Readiness
Support for ISO/IEC 17025 & 17034 journeys.
Global Footprint
Partners and projects across Europe, the Middle East, and Asia ensure timely, compliant supply and support for your programs.