Chemical Industry
Contract Research Organizations
Pharmaceuticals
QC & Validation
21 CFR Part 11
GLP
GMP
ISO 17025
Method Validation
Full ICH Q2(R1) / USP <1225> method validation across 8 parameters: specificity, linearity, accuracy, precision, range, LOD/LOQ, robustness. 10-step protocol with signature chain.
Use this template