Supplement Ingredient Sourcing
APEX CSM qualifies, purchases, and releases high-purity raw materials through a vetted global network. Every lot is traceable with signed COAs and risk-based testing—so launches stay compliant, consistent, and on schedule.
Built for Speed, Confidence, and Scale
The APEX sourcing model compresses timelines without compromising quality. Our qualified suppliers, disciplined QA, and clear checkpoints help you move from brief to batch with fewer handoffs.
Fast Lead Times
Priority access to common actives and packaging plus proactive testing plans to keep ETAs realistic and reliable.
Flexible MOQs
Right-size each buy: pilot runs for proof, then scale with predictable costs and stable quality as demand grows.
FDA & cGMP-Certified Network
Audited facilities and ISO/IEC 17025 partner labs to safeguard identity, potency, purity, and micro compliance.
Our Sourcing Process
A clear, accountable path from requirements to release. You’ll always know what’s next, what’s needed, and when you ship.
Requirements
Target assay, solvents, micro limits, labeling claims, allergen and market-specific constraints.
Qualification
Supplier questionnaire, document review, quality agreements, audits or equivalency assessments.
Spec Lock
Approved specifications, methods, and acceptance criteria for lot release and ongoing monitoring.
Intake & Testing
Identity testing plus risk-based micro, heavy metals, residual solvents, and contaminants as applicable.
Release
Traceable COAs, chain-of-custody, batch records, and performance scorecards with CAPA when needed.
Quality, Documented
Expect transparent documentation at every milestone. We maintain batch records, test results, and label proofs aligned to retailer and marketplace expectations—so your listings stay live and audits stay predictable.
- Identity, potency, and purity to spec
- Microbial & heavy-metal screening as required
- Stability guidance by dosage form
- COAs and lot traceability on release
Sourced Categories
- Vitamins, minerals, aminos
- Botanicals & extracts
- Lipids, enzymes, probiotics
- Sweeteners & flavors
Documentation
- Signed COAs & specs
- Non-GMO / vegan statements
- Country-of-origin & Organic (as available)
- Allergen & residual solvent status
R&D & Compliance
- Form selection & bioavailability
- Label claim feasibility
- Prop 65 strategy
- Sports screen (risk-based)
Logistics
- Safety stock planning
- Reorder triggers
- Freight mode options
- Retail & DTC workflows
Certifications & Quality Assurance
- FDA- & cGMP-certified facilities
- ISO/IEC 17025 partner labs; compendial methods where applicable
- HPLC, ICP-MS, GC, FTIR, and microbiological testing as required
- Change control, CAPA, and continuous improvement
FAQs
Straight answers to the most common sourcing questions.
Can you match our existing spec?
Yes. Share target assay, limits, preferred methods, and claims. We’ll qualify equivalent or superior sources and provide COAs for approval.
Do you provide Non-GMO, vegan, or Organic documents?
We obtain supplier declarations and certificates when available and retain them with the lot record. Organic availability depends on ingredient and market.
How do you manage lead times?
Quotes reflect supplier capacity, testing requirements, and freight mode. For repeats, we can set safety stock or reorder triggers to protect supply.
Can you source patented or trademarked actives?
Yes. We work with brand owners and authorized distributors to secure licensed use and correct trademark attributions for labels and marketing.