We offer seasoned acumen and expertise in both development and manufacturing, with advanced technological capabilities and the innovative protocols with agile business models to overcome development hurdles and speed your products to market, no matter what challenges may arise.

Our development and cGMP manufacturing capabilities are geared towards nutraceuticals,  dietary supplements, vitamins, proteins, and skincare.  Our formate includes liquid, soft-gel encapsulation, capsules, and powder. Our packaging and fulfillment solutions vary upon our clients requirements from bottles, blister pack, to sleeves.

Our end-to-end process begins with in-depth analysis and strategic critical paths curtailed around your target requirements and product.  Our library of formulas and protocols is vast and robust. We are experts in our explicit ability to accelerate nutrient bioavailability to cells in the body.  All product formulation, development, and manufacturing protocols entails lyophilization or hydrolization to unbind and free amino acids found in peptides derived from plants, or animal sources. This includes studies with accelerated stability (stress) studies, stability-indicating analytical method development, and other physiochemical characterizations designed to pinpoint potential product candidate stability problems and enable formulation optimization.

• Comprehensive biomarker of physicochemical properties
• Estimate a product’s stability when exposed to various common stresses
• Establish stability assays to outline major degradation rates
• Decide upon a lyophilized or hydrolyzed formulation for initial clinical studies
• Finalize a formulation development research protocol (matrix of buffer, pH, stabilizer, tonicity modifier; analytical methods; etc.)

We encompass a robust variety of R&D services to help formulate your product:

• Analytical Methods
• Formulation Development
• Lyophilization Cycle Development
• Hydrolization Cycle Development
• In Use, Compatibility, and Robustness
• Technology & Innovation
• Modalities & Stability Studies

Our robust library of formulas and protocols affords us the ability to create and co-create new intellectual properties by way of licensing.  Our IP strategy and monetization framework is comprised of three pillars:

I. Limited Rights & Uses Of Our Formulas & Protocols In R&D Collaborations

II. PRIVATE LABEL; the purchase of our stock formulas with your logo on the label

A. We provide end to end private labeling solution from concept, to manufacturing, packing, fulfillment

B. We provide the finished formula in bulk client packages and fulfills

III. TRANSFER OF TECHNOLOGY (TOT); we transfer our intellectual property to another organization (licensee) via a licensing agreement whereby the licensee attains a right to use the technology for a fixed period of time by paying a particular fee for it.