Transparency is the foundation of clinical research. Every batch of Forged Pharma compounds undergoes rigorous, independent third-party analytical testing to guarantee absolute purity, precise concentration, and the absence of heavy metals or biological contaminants.
Standard
99%+ Purity
Methodology
HPLC-UV / MS
We utilize industry-standard pharmacological testing protocols to ensure our researchers receive exactly what is on the label. Our multi-phase verification process leaves zero room for guesswork.
High-Performance Liquid Chromatography separates the compound into its individual components. This allows us to verify the exact concentration (mg/ml) and ensure the active pharmaceutical ingredient (API) matches the label claim with >99% accuracy.
By measuring the mass-to-charge ratio of ions, Mass Spectrometry provides a definitive molecular fingerprint of the substance. This confirms the absolute identity of the compound, ensuring no substitutions or degradation has occurred.
Beyond purity and concentration, our raw materials undergo strict screening for heavy metals (lead, arsenic, mercury) and microbial pathogens. All injectable carrier oils are further sterilized to pharmaceutical standards to prevent injection-site complications.
Understanding the data on our certificates guarantees confidence in your research protocol.
Verify the "Analyte" or "Compound Name" matches exactly what you ordered.
Look at the chromatogram peak area. We require a minimum of 99% baseline purity.
For liquids/orals, ensure the tested mg/ml or mg/tab matches the label dosage claim.