Quality Control
Every Batch. Independently Verified.
Forge Scientific was built around one principle: researchers deserve to know exactly what they’re working with. Here’s how we verify the identity, purity, and integrity of every product we offer.
Process
Our Quality Process
Here’s how Forge Scientific approaches quality verification at every stage.
Source Selection
We work with a limited set of manufacturing partners selected for consistency and documentation practices, not just price.
Independent Lab Testing
Whenever applicable, incoming batches are sent to independent third-party laboratories for analytical verification rather than relying on supplier-provided data alone.
Purity & Identity Analysis
Testing methods such as HPLC (High-Performance Liquid Chromatography) and mass spectrometry are used to confirm compound identity and measure purity.
Documentation & Release
Only after a batch’s results are reviewed is it moved into sellable inventory, with its Certificate of Analysis published for researchers to reference.
Why Batch Testing Matters
Research outcomes depend on knowing exactly what’s in the vial. Variability in purity or identity between batches can undermine reproducibility — which is why documentation matters as much as the material itself.
Each batch is checked against its expected identity and specification before being made available.
Batch-specific Certificates of Analysis are made available so researchers aren’t relying on marketing claims alone.
Testing practices are applied uniformly across products and reordered batches, not just on a sample basis.
Every vial is labeled with a lot number that maps directly back to its corresponding test documentation.
View Certificates of Analysis
Match the lot number on your vial to its corresponding COA and see the full test results for your batch.
View COAsFrequently Asked Questions
Common questions about our testing process and how to read your Certificate of Analysis.