KERNOLOGIX

Kernologix LLC · Richmond, Virginia

cGMP botanical ingredients for North American manufacturers.

B2B wholesale distribution of high-purity botanical raw materials, active cosmetic ingredients, and nutraceutical extracts — US-warehoused, specification-verified, and documented at the lot level.

Company Overview

Kernologix LLC specializes in sourcing and distributing strictly US-warehoused, cGMP-compliant botanical ingredients for dietary supplements and cosmetics. We supply contract manufacturers and brand owners who require industrial volumes, standardized assays, and documentation that QA can release against a written specification.

Quality & Regulatory First

Quality operations are governed by the Kernologix Quality Management System (KLX-QMS). Controls are aligned to FDA 21 CFR Part 111 (dietary supplements) and 21 CFR Part 117 (preventive controls for human food), including standardized specification verification and lot-level Certificate of Analysis documentation for every release.

  • Specification match before offer: identity, assay, and impurity limits versus the buyer or Kernologix material spec.
  • Lot-level CoA retained and transmitted with fulfillment — not a generic product sheet.
  • KLX-QMS documentation aligned to 21 CFR Parts 111 and 117 for dietary supplement and food-facility preventive-control context.

Clinical & Technical Leadership

Kernologix was founded and is led by Harika Vemulapalli, Pharm.D. (PTCB Certified). Procurement and quality control are directed by clinical pharmacy leadership, with emphasis on technical precision, purity verification, and supply-chain integrity rather than commodity brokerage.

Supply Chain Model

We partner with verified domestic cGMP warehouses to provide drop-shipped raw-material fulfillment directly to contract manufacturers (CMOs) across North America. Inventory remains in qualified US facilities; Kernologix coordinates specification release, documentation, and logistics so the manufacturer receives a lot-identified, CoA-backed shipment at the dock.

Core Values

Analytical Verification

Incoming lots are released against standardized specifications. Assay, identity, and impurity data are reviewed before material is offered to contract manufacturers.

cGMP Compliance

Sourcing and documentation follow KLX-QMS controls aligned to FDA 21 CFR Parts 111 and 117. Partner warehouses are verified domestic cGMP facilities.

Transparent Supply Chain

Lot-level Certificates of Analysis accompany every shipment. Traceability is maintained from warehouse release through drop-ship fulfillment to the CMO dock.

Commercial inquiries

Specification packets, lot availability, and CMO drop-ship coordination are handled by operations. Headquarters: Richmond, Virginia.