Beyond the ordinary

Our formulations are engineered for precision, combining clinically studied ingredients with pharmacokinetic modeling to optimize efficacy. Each blend is designed to support targeted biological pathways while minimizing redundancy and metabolic interference.

We source exclusively from suppliers who meet rigorous standards for GMP certification, kosher compliance, and ingredient traceability. Vendor audits include documentation of origin, processing methods, and third-party verification.

Every ingredient is traceable to its country of origin, cultivation method, and extraction process. We maintain full documentation including COAs, batch records, and kosher source files to ensure transparency and halachic integrity.

We use standardized extracts and compounds to ensure consistent potency across batches. Active constituents are verified using HPLC, UV spectrometry, or mass spectrometry depending on compound class.

Ingredients are selected for molecular uniformity, minimizing variability in absorption and bioactivity. We reject raw materials with inconsistent particle size, polymorphic instability, or unverified chirality.

Our blends are designed for biochemical synergy, ensuring that co-factors, enzymes, and transporters work in concert. We avoid antagonistic pairings and prioritize metabolic harmony.

Each product is mapped for compatibility with other supplements in our lifecycle-sensitive stack. We evaluate nutrient timing, absorption pathways, and potential interactions to support safe, effective layering.

We assess ingredient stability under heat, humidity, and light exposure. Sensitive compounds are encapsulated or buffered to prevent degradation and preserve therapeutic value.

Shelf life is determined through accelerated stability testing and real-time degradation modeling. We publish expiration dates based on validated potency thresholds—not marketing estimates.

Antioxidant-sensitive ingredients are protected using nitrogen flushing, opaque packaging, and microencapsulation. We monitor peroxide values and oxidation markers during production and storage.

We avoid common allergens including gluten, dairy, soy, and shellfish unless explicitly declared. Allergen segregation protocols are validated through swab testing and batch-level documentation.

Manufacturing partners follow strict GMP protocols for equipment cleaning, air filtration, and ingredient isolation. We require validated cleaning logs and allergen risk assessments for every production run.

All products are manufactured in FDA-registered facilities that comply with 21 CFR Part 111. Facilities undergo routine inspections and maintain electronic batch records for traceability.

Capsules are tested for disintegration using USP <2040> protocols. We ensure that active ingredients are released within the optimal window for absorption in the gastrointestinal tract.

We map ingredient release profiles based on pH sensitivity, capsule coating, and digestive transit time. This supports targeted delivery to the stomach, small intestine, or bloodstream.

We only work with facilities that are GMP-certified by third-party organizations such as NSF, USP, or Eurofins. Certification includes audits of sanitation, documentation, and quality systems.

Each batch undergoes in-process QC checks including weight variation, capsule integrity, and moisture content. Deviations trigger root cause analysis and corrective action protocols.

QA teams review all documentation, test results, and supplier certifications before product release. This ensures compliance with internal specifications and regulatory standards.

Finished products are tested by independent labs for identity, potency, microbial load, heavy metals, and residual solvents. We publish results upon request for full transparency.

We use vegetarian capsules unless lifecycle-sensitive gelatin is required and certified. Capsule size, coating, and disintegration are optimized for absorption and communal accessibility.

Dosages are based on clinical research, bioavailability studies, and lifecycle needs. We avoid megadosing and prioritize therapeutic ranges that support long-term resilience.

We reject ingredients with synthetic fillers, artificial colors, or unverified excipients. Purity is confirmed through third-party testing and supplier documentation.

We use HDPE or amber glass bottles to protect against UV degradation and moisture intrusion. All packaging is BPA-free and selected for stability and recyclability.

ll ingredients are certified by trusted Orthodox agencies. We maintain editable source files (PDF, AI, INDD, EPS) for every kosher symbol used, ensuring future-proofed compliance and communal trust.