Analytical Testing
Our analytical laboratory provides a comprehensive range of services designed to ensure product quality, safety, and regulatory compliance. From advanced impurity profiling and nitrosamine testing to method development, validation, and transfer, we deliver accurate and reproducible results. With expertise spanning pharmaceuticals, supplements, and raw materials under international pharmacopoeia standards (USP, BP, EP, IP, JP), we help clients achieve faster approvals, stronger compliance, and greater market confidence.
- Nitrosamine testing
- Cleaning validation
- Method Development / Validation & Transfer
- Element analysis
- Assay test for pharmaceuticals and supplements products
- Stability studies
- Raw Material Characterization as per latest Pharmacopoeia (USP / BP / EP / IP / JP)
- Impurity Profiling: Method Development, validation and testing
- HPLC to UPLC method transfer
- Qualification of Standards: Preparation, Characterization & Establishing Assay (Potency Determination)
- Bioanalysis
- ISO 7025
- ISO 9001:2015
- ILAC-MRA
- JFDA GLP/GCLP
- 21 CFR Part 11

