Our 4 Step Process

Quality Assurance Certification

Every Charge formulation begins with a clear question: What dose is supported by evidence to produce a meaningful effect? From there, the formula is built around validated ranges, bioavailability, and functional synergy, not profits.

Before any product carries the Charge name, it progresses through a defined multi-step Quality Assurance process:

Step 1 - Individual Ingredient Testing

All raw materials are sourced against predefined specifications and supplier qualification criteria. Each ingredient is verified for identity, purity, and safety through documented testing and traceable batch records prior to production release.

Step 2 - Efficacy Validation

Ingredient inclusion levels are determined using available clinical literature and established dosing ranges. We assess bioavailability, mechanistic rationale, and cumulative formulation impact to ensure each component contributes meaningfully to the intended outcome.

Step 3 - In-Process Manufacturing Monitoring

Production occurs under controlled conditions with monitored weighing, blending, and filling procedures. Critical control points are assessed to maintain batch-to-batch consistency, uniformity, and label accuracy from first unit to last.

Step 4+ - Continuous Refinement

Scientific understanding evolves. Our formulations are periodically reviewed against emerging research and updated standards to ensure they remain aligned with current evidence and best practice.

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