Supplements are one of the fastest-growing consumer categories today —...
Read MoreSupplement Manufacturing
Reliable supplement manufacturing starts with the right factory, the right formulation, and zero shortcuts on compliance.
How Sourcify Supports Your Supplements Sourcing
We operate as your sourcing team — protecting quality, compliance, and momentum.
Vetted GMP Facilities
Factories screened for real GMP execution, not marketing claims.
Formulation & Scale Guidance
Support on excipients, bioavailability, and manufacturability before you commit.
Compliance & QC Oversight
COAs, stability data, labeling alignment, and audit preparedness.
Multi-Factory Backup Planning
Contingency options to prevent supply chain disruptions.
Ongoing Issue Resolution
We stay involved after the intro — fixing problems before they escalate.
Best Countries for Manufacturing Supplements
United States
Canada
China
India
United States
Ideal For: Brands prioritizing compliance, retail readiness, or investor scrutiny
Cost Snapshot: High
Lead Times: 8–16 weeks
Canada
Ideal For: Premium or clinically positioned brands
Cost Snapshot: Medium–High
Lead Times: 10–18 weeks
China
Ideal For: Cost-sensitive products with strong QC oversight
Cost Snapshot: Low–Medium
Lead Times: 12–20 weeks
India
Ideal For: Ingredient-forward or bulk supplement lines
Cost Snapshot: Low
Lead Times: 14–22 weeks
Ready to Start Your Supplements Project?
Clarity, compliance, and factories you can trust without the guesswork.
Supplement Types We Support
We support a wide range of supplement formats, each with different formulation, manufacturing, and compliance requirements.
Capsules
Hard-shell and veggie capsules require precise blend uniformity, flow control, and encapsulation accuracy.
Tablets
Compressed formats where tooling quality, binder selection, and hardness testing directly affect performance and shelf life.
Powders
Stick packs, tubs, and sachets that demand tight controls on particle size, moisture, and flavor masking.
Liquids & Tinctures
Alcohol- or glycerin-based formulas with stricter microbial controls and packaging compatibility needs.
Gummies
High-risk formats requiring expertise in gelatin or pectin systems, heat control, and stability management.
Softgels
Oil-based supplements that require specialized encapsulation equipment and oxidation management.
Key Manufacturing Risks to Avoid
Most supplement issues don’t show up at launch, they show up at scale.
Inconsistent Potency
Poor blend uniformity or inadequate testing leads to failed COAs and recalls.
Non-Compliant Labeling
Structure/function claims or missing disclosures can trigger FDA warning letters.
Weak Stability Data
No real shelf-life testing puts expiration dates and trust at risk.
Ingredient Substitution
Unauthorized swaps to cheaper raw materials compromise efficacy and compliance.
GMP Gaps
Facilities that claim compliance but lack real documentation or audit readiness.
When Brands Seek a New Manufacturer
Founders usually don’t switch factories lightly.
- Failed third-party lab results
- Inconsistent batches or flavor drift
- Missed production timelines
- Poor documentation or audit readiness
- Ingredient sourcing opacity
- Scaling issues at higher MOQs
- Labeling or regulatory violations
- Communication breakdowns
- Rising costs without explanation
Frequently Asked Questions
Real compliance shows up in documentation, audit readiness, testing protocols, and batch records not just certifications on a website.
MOQs vary by format, but most start between 50,000–200,000 units depending on complexity and geography.
Yes, but it increases coordination risk. Many founders underestimate how ingredient sourcing affects batch consistency and timelines.
From formulation finalization to finished goods, expect 8–20 weeks depending on location and testing requirements.
Yes. We flag formulation issues early and help adjust before they become expensive problems.
Recent Supplement Blogs
Ready to Start Your Supplements Project?
Clarity, compliance, and factories you can trust without the guesswork.
