RapID can scan through multi-layer paper sacks in seconds
RapID Raw Material ID Verification System (Discontinued)
The RapID Raman system is a solution for raw material testing in pharmaceutical GMP quality control. RapID is a portable scanner that uses Agilent spatially offset Raman spectroscopy (SORS) to enable high-throughput raw material analysis through a range of container types—including plastic barrels and paper sacks.
With conventional techniques, raw material testing in opaque containers can create a bottleneck in pharmaceutical manufacturing. A dedicated sampling area is needed to open, sample, test, and reseal each container to verify the identity of the contents. The RapID system allows the operator to verify the contents of each container through opaque and colored packaging enabling release immediately into production.
The Vaya handheld Raman spectrometer is the latest Agilent product for through barrier raw material identity verification. Vaya provides the through barrier capabilities of RapID but in a more compact and convenient, handheld form.
With conventional techniques, raw material testing in opaque containers can create a bottleneck in pharmaceutical manufacturing. A dedicated sampling area is needed to open, sample, test, and reseal each container to verify the identity of the contents. The RapID system allows the operator to verify the contents of each container through opaque and colored packaging enabling release immediately into production.
The Vaya handheld Raman spectrometer is the latest Agilent product for through barrier raw material identity verification. Vaya provides the through barrier capabilities of RapID but in a more compact and convenient, handheld form.
This product is discontinued effective 1 August 2025. See product replacement—the Vaya Handheld Raman Spectrometer
Product Details
Features
- Expand your capabilities: mobile Raman ID through opaque and transparent containers
- Accelerate workflows: provides fast ID workflow and 100% ID testing for all incoming containers
- Simplify processes: avoid time-consuming sampling procedures and optimize raw material quality
- Reduce risks: maintain sterility, prevent cross-contamination, and eliminate operator exposure through non-invasive analysis. Streamline sterile manufacturing of parenteral and biological products
- Adapt with versatility: compatible with most APIs, excipients, and containers—like multilayer paper and plastic sacks, opaque plastic drums, and thick amber glass bottles
- Meet data integrity standards: facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11, and similar national electronic record regulations
How It Works
