Frequently Asked Questions

Insights into Our Capsule CDMO Capabilities

We specialize in manufacturing a wide range of dietary-supplement capsule products, including vitamins, minerals, herbal extracts, probiotics, prebiotics, and postbiotics. Our portfolio is particularly strong in formulations designed for gut health, urinary tract health, longevity, and healthy aging / anti-aging applications. Whether you need simple single-ingredient capsules or advanced multi-ingredient blends, we can support your product development goals.

Yes. We regularly support R&D batches, pilot batches, and small-scale production runs to help brands validate new formulations, conduct preliminary stability testing, and perform market testing prior to full commercial scale-up. Our flexible operations are designed to grow with your brand.

Our manufacturing facility is fully cGMP-compliant and operates under FDA oversight in accordance with 21 CFR Part 111 (dietary supplements) and 21 CFR Part 211 (finished pharmaceuticals where applicable). We maintain strict quality systems, validated processes, and robust documentation to ensure product consistency, safety, and regulatory readiness.

Yes. We provide full turnkey capsule manufacturing services, including:

  • Bulk or bottled capsules
  • Labeling and shrink-seal application
  • Packaging design support
  • Retail-ready packaging solutions
  • Private-label and white-label programs

This allows brands to go from concept to market using a single integrated manufacturing partner.

Our standard MOQs start at 500–1,000 bottles per SKU, making us an ideal partner for emerging brands or pilot launches. For more competitive pricing and optimized production efficiency, we recommend batches in the range of 2,000–10,000 bottles. We are happy to advise on volume planning based on your market strategy.

Absolutely. Our scientific and formulation team can assist with full custom formulation
development tailored to your desired benefits, ingredient profile, and marketing claims.

We also specialize in:

  • Vegan / HPMC capsules
  • Gluten-free and allergen-free formulations
  • Clean-label and plant-based ingredient systems We work closely with you to develop formulations that meet both functional and regulatory requirements.

Standard production lead time is typically 10–12 weeks, depending on ingredient availability, packaging components, and formulation complexity. Once your formula, packaging specifications, and volumes are finalized, we provide a detailed project timeline for transparent planning.

Yes. Every production batch is released with a Certificate of Analysis (CoA) verifying identity, purity, potency, and microbial safety as applicable. We also offer stability testing support to help establish shelf life, packaging suitability, and long-term product performance.