The Regulatory Demand for 100% Raw Material ID
GMP regulations mandate that pharmaceutical companies verify the identity of every single container of incoming active ingredients and excipients. Traditional laboratory testing requires opening bags, collecting samples, and waiting for HPLC validation, creating high labor costs and contamination risks.
Instant Dock Door Scans
Using USTECH handheld spectrometers and caliX PCA classification models, operators scan chemical powder bags directly through transparent packaging at warehouse dock doors. The system validates the material identity against a database of verified chemical profiles instantly.
References
- European Pharmacopoeia 2.2.40 - Near-Infrared Spectroscopy.
- "Implementing 100% Receiving Dock Raw Material Verification using Handheld MEMS Spectrometers," Journal of Pharmaceutical Innovation, 2023.